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		<id>https://wiki.dmt-nexus.me/Known_substance-interactions_and_their_effects</id>
		<title>Known substance-interactions and their effects</title>
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				<updated>2014-08-05T16:43:24Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* AM-2201 + MDMA */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{ShowInfo|[[Image:Error.png]]|'''WARNING:'''|'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
This article is about the interactions and effects of  mixing different entheogens, both with each other and with medicine. Some combinations have a good synergy while others can be a DEADLY combination! Taking any substance carries a high responsibility, please read the WARNING section with great care!&lt;br /&gt;
&lt;br /&gt;
== Warning! ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: orangered;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&amp;lt;br /&amp;gt;&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: red;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Even though the interactions of certain substances are described here, it is extremely important to be safe at all times! This article is only to give information about interactions and their effects, '''this article is NOT meant for advice on taking any combination!'''&lt;br /&gt;
&lt;br /&gt;
Many interactions described here are ''subjective descriptions'', so what is shown here is only an ''indication'' on how certain combinations can affect you and how safe they are. Many times those effects are dependent on dose (of each substance), route of administration, timeline of administration, set and setting, your mood, your physical health, your mental health and many other factors. &lt;br /&gt;
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== Psychedelics ==&lt;br /&gt;
&lt;br /&gt;
=== DMT ===&lt;br /&gt;
&lt;br /&gt;
Some report dysphoria at lower doses. I (House) do not find this to be the case I find low doses incredibly euphoric. Higher doses can be known to go beyond human emotions and concepts. Higher doses of DMT are also known to cause strange bodily hallucinations like the feeling that you have stopped breathing, or that your heart has stopped beating. These hallucinations are common and can be countered with conscious relaxation and meditation prior and during the experience. You do not have to submit, per se, but beware that you may have to let go of certain intensities during the experience. It can easily be the most &amp;quot;intense&amp;quot; experience of your life for some people, and this is *NOT* a bad thing!&lt;br /&gt;
&lt;br /&gt;
==== DMT + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Alcohol|#805000|#E0A040|SAFE But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|I find that combining the spice with a carcinogenic neurotoxin like [[alcohol]] completely negates the experience and masks it with toxic nullification (Yes, I am quite biased)}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The alcohol did  have a negative impact on me. I tried to drink a few beers beforehand to mitigate the anxiety of the [[pharmahuasca]] but that only resulted in dulling down, confusion and nausea.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|The Spice doesn't like Alcohol, you'll either wont remember or get a bad vibe.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + Benzodiazepines (Xanax) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + enzodiazepines|#406040|#FF6060|BAD IDEA!|....|&lt;br /&gt;
{{UserDescription|stoopkidpzpz|[[Image:negative.png]]|I took 1 MG of Xanax, and felt relaxed in about an hour.&lt;br /&gt;
Decided to smoke some enhanced leaf... I smoked A LOT... I re-dosed for about 2 straight hours, 100mg doses each time.&lt;br /&gt;
When I was finished I took another 1 MG of Xanax... &lt;br /&gt;
A few hours later I became mildly confused, got a SEVERE headache, the worst I have ever had in my life. I had crippling nausea, could barely walk straight.. Ended up projectile vomiting multiple times until I fell asleep..}}&lt;br /&gt;
}}&lt;br /&gt;
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==== DMT + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK, although some people don't like it. If you are a daily cannabis smoker it shouldn't be a problem, but if you get anxiety from using [[Cannabis]] occasionally it may be wise not to mix it with [[DMT]].}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:neutral.png]]|If I smoke DMT / Changa 1-2 hrs after my last hit of cannabis it is great, if I smoke DMT &amp;amp; Cannabis together it is not so great.}}&lt;br /&gt;
{{UserDescription|Entheogenerator|[[Image:neutral.png]]|I always enjoyed DMT + cannabis when I was a daily cannabis smoker. At that time it worked to reduce anxiety and made it easier for me to relinquish control of the situation and allow the DMT to take over. Cannabis does not typically cause anxiety for me when it is used alone. But now that I only smoke cannabis on occasion (5-10 times a year), combining the two tends to cause a lot of anxiety and fear for me. I find that a puff or two of cannabis during the tail end of the DMT afterglow can help with integration, but I can no longer smoke cannabis prior to or at the same time as DMT.   }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + Dissociatives ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Dissociatves|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|By far my absolute favourite combination. This experience is equal in intensity as DMT but without the ego loss. An entirely new realm all together where YOUR controller. This can mean many things, its sheer awesomeness with seemingly no downside gives it quite an addictive quality. During my first encounters with this combination I probably went through more DMT in one night then I normally would have in months, maybe a year.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Harmalas (MAOI)|#406040|#60FF60|OK|[[Harmalas]] potentiate and prolong the effects of [[DMT]], while at the same time it adds a slight psychedelic effect of it's own. For DMT to be orally active, a [[MAOI]] is mandatory.|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Oral activation. Potentiation. Slowed-down effect. The two go hand in hand creating a perfect synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + LSD ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Negative.png]]|I didnt like it at all because it felt like LSD acts as an anchor and holds one down, preventing breakthrough}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Euphoric, not as deep of a trip, but there is zero anxiety present which can be useful and awesome in it's own right.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Mescaline|#406040|#60FF60|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy here. Potentiates the [[mescaline]] and smooths it out.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Neutral.png]]|The mescaline seems to 'dull' the [[DMT]]. So there was not as much effects from smoking the DMT on Mescaline as you would expect.}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Negative.png]]|The mescaline seemed to hold the [[DMT]] towards the center of the vision, as if it didnt let it &amp;quot;expand&amp;quot;. I saw the DMT visuals curling up, like as if a magnetic/gravitational force didnt let it happen freely. The trip felt weird, it didnt feel 'natural' or 'flowing' to me. Tried it twice in different occasions to similar results and didnt feel like it's a good combination for me}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DMT + Mushrooms (psilocybin) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Mushrooms (psilocybin)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Another profound synergy that seems to unlock the potential of the [[mushroom]]. Either @ peak or after.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Positive.png]]|When DMT is smoked at the peak or post-peak of mushrooms, there is an extreme synergy that can make it for an incredible experience that can take one very very far! My favourite combo}}&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized DMT whilst on mushrooms- Potentiation, intense synergy between the two tryptamines, very strong visuals came thick and fast.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== DMT + Suboxone (Buprenorphine + Naloxone) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Suboxone|#406040|#60FF60|OK|....|&lt;br /&gt;
{{UserDescription|Entheogenerator|[[Image:neutral.png]]|I used DMT several times while on a daily Suboxone maintenance program, and the Suboxone did not have any noticeable effect on the DMT experience. I did not notice any difference between vaporized DMT with Suboxone and vaporized DMT without Suboxone. This may only apply to a person who is undergoing regular buprenorphine treatment and has developed a tolerance to the effects of buprenorphine to the point that it does not produce a &amp;quot;high&amp;quot;. If a person without any tolerance to opiates/opioids were to take buprenorphine and then smoke/vaporize DMT, it may dull the effects of DMT to some extent as other opiates/opioids seem to.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Harmalas (MAOI) ===&lt;br /&gt;
&lt;br /&gt;
Side effects include contraindication with certain substances. Make sure you understand interactions with substances before using them! At higher doses users experience nausea and vomiting, but this also isn't necessarily a bad thing, since harmalas are anti-parasitic, purging is often considered cleansing to both the body and the mind. Chest pressure is also common with ayahuasca. Feelings of having something heavy sitting on you. This is normal and if experienced just relax and let it be, it's part of the serpents coil.&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas + caffeine|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally don't mind a low dose of harmalas on top of caffeine, it can counter act the sedation from the harmalas in the right dosages. Too much of both and you will experience uncomfortable heart rate. So new users to this synergy take caution and start low!}}&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|I had one cup of average strength coffee about 2 hours after smoking changa and I got very edgy and nervous. Coffee barely even wakes me up but I was wired for about an hour. Quite uncomfortable.}}&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|For me, a cup of yerba matè plus ayahuasca equals awful experience. There seem to be some people who can't take caffeine and ayahuasca}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Oral Harmalas (MAOI) + 5-MeO-DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas + 5-MeO-DMT|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|this could be hard on some metabolism, or dangerous, but IME, a great form of pharmahuasca, more nausea than with N,N-DMT, but also more euphorie.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Neutral.png]]|Harmalas will significantly increase potency of 5-MeO-DMT. 40-60mg harmaline + 10mg 5-MeO-DMT orally is equivalent to 30-35mg oral 5-MeO-DMT by itself or 10 mg intranasally (see Ott 2001 Note that 35mg by itself was not active dosage to shulgin but was for ott}}&lt;br /&gt;
{{UserDescription|Picatris|[[Image:Negative.png]]|Potentially unsafe combination and health risks due to metabolic issues. For more info search the forum for the thread titled &amp;quot;Does Anyone Here Eat 5-MEO-DMT?&amp;quot;.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + Kava kava ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas + Kava Kava|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + Opioids ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Oral Harmalas (MAOI) + Opioids|#604040|#FF6060|BAD IDEA!|Has the potential for adverse reactions, namely CNS excitation or depression (resulting in high or low blood pressure).|&lt;br /&gt;
}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + L-dopa ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas + L-dopa|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|taking levodopa with MAOIs runs the risk of a hypertensive crisis and levodopa should not be taken for at least 2 weeks after MAOIs; the risk of taking RIMAs (specifically moclobemide) with levodopa is one of increased side effects which include anorexia, nausea, vomiting, agitation, postural hypotension, tachycardia, arrythmias, hypomania, psychosis, depression, headache, flushing, gastrointestinal bleeding, itching, rashes, abnormal involuntary movements. &lt;br /&gt;
&lt;br /&gt;
The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinations}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Oral Harmalas (MAOI) + tyrosine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas + tyrosine|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|l-tyrosine taken with MAOIs renders it more likely to be a vasopressor ie cause an elevation in BP.&lt;br /&gt;
&lt;br /&gt;
The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinationss}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + Dissociatives ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + Dissociatives|#604040|#FF6060|BAD IDEA!|Even though there are reports on the net of people combining MXE with harmalas, in the right dosages harmalas + dissociatives have the potential to cause cardiac arrest.|}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + Corticosteroids / Prednisone ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Oral Harmalas (MAOI) + Corticosteroids / Prednisone|#604040|#FF6060|BAD IDEA!|If you have been on prednisone for more than a couple of weeks you should NEVER stop the treatment abruptly; the dose should always be tapered down to allow your adrenal gland to 'wake up' and start producing glucocorticoids again.&lt;br /&gt;
&lt;br /&gt;
Harmala alkaloids inhibit CYP3a4 which has a role in metabolising prednisone, so the combination can magnify the effects of the steroid including adverse effects on glucose tolerance and lipid profiles.).|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Mushrooms (psilocybin) ===&lt;br /&gt;
&lt;br /&gt;
I (House) think the most common side effect I hear about with shrooms is stomach discomfort. A lot of people don't know that you really are not supposed to consume any kind of raw mushroom. It's a rare case in the culinary and medicinal fields where raw mushrooms are told to be ingested. (I can think of a few exceptions, of course.) So for some ingesting the raw material can be very nauseating, myself included. Making a tea or the lemon tek is the way to go. By soaking raw mushrooms in lime juice, the citric acid literally cooks the mushrooms breaking down the cell walls. This is also known as a ceviche in the cooking world. Personally I just slip the shot of lime juice with the mushrooms in it back, it tastes good and I don't experience nausea this way. Some people filter out the mushroom material from the solution. Experiment. Taking too many mushrooms can lead to a feeling of being poisoned, but as far as I know no one has ever died from taking them on their own. Dose accordingly!&lt;br /&gt;
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&lt;br /&gt;
==== Mushrooms + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I won't use mushrooms without cannabis; Noticeable synergy and eases any anxiety present. Some people who don't use cannabis often find that this combo causes paranoia.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Mushrooms + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Profound synergy. Great for meditation and dance}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Harmalas (MAOI)====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Harmala (MAOI)|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love the harmala + mushrooms synergy, but some have noted that the harmalas potentiate the mushrooms very much and have had rough trips! If you want to experiment with this combo, start low and work your way up!}}&lt;br /&gt;
&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Neutral.png]]|I tried this combo at a fairly high dose, it GREATLY potentiated the effects.. And I absolutely loved it, quite more then the intensity I was looking for. Although after the first 6 hours, I felt the trip had come to conclusion, I was ecstatic, but physically and mentally exhausted, only to have the experience continue at practiaclly the same intensity for ANOTHER 6 hours. Before I could get any sleep whatsoever.  If you try this combo, its great, just be prepared to trip for a LONG time.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Mushrooms + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Alcohol|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, slower than cocaine however. Also, people tend to get negative from this combo. One might hypothesize that alcohol tends to turn the trip in a darker direction.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad idea, high chances to end up puking and feeling miserable.}}&lt;br /&gt;
{{UserDescription|Frankycou|[[Image:Negative.png]]|This is potentially very unsafe! some type of mushroom are known to develop poison when mixed with alcohol. This is very rough information that I am reporting since I don't remember the exact text and source but basically I read from a reputed source that some types are EXTREMLY BAD  to mix and should be avoided at all cost.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Alcohol + Cocaine + MDMA====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Alcohol + Cocaine + MDMA|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad bad idea. I took the MDMA, Coke and Alcohol at the end of a Shrooms trip. Anxiety and profound guilt were felt in my whole body}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Cocaine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Cocaine|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, or even stop it dead in it's tracks.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== LSD ===&lt;br /&gt;
&lt;br /&gt;
LSD is a potent vasoconstricting substance. This means it causes an increase in blood pressure by tightening the blood vessels in the body. This can be countered with vasodilating substances. Some find that oral hash completely diminishes the vasoconstriction. I like using transdermal magnesium prior to a dose to also help with things like jaw tension. Also, conscious relaxation, deep breaths, and massage (even done by the self) can help curb tension experienced from the drug. If you feel over stimulated or uncomfortable, you probably need to &amp;quot;Flow&amp;quot;, so to speak. Get up, stretch, dance around, laugh, have an orgasm, be creative, play a musical instrument, take a hot shower. Things like this help with getting energy flowing and making meditation easier. Eat a bit of fruit on the come-up if you feel some unease! Many people find cannabis greatly eases the transition, but of course not everybody. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + Ayahuasca + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Ayahuasca +DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is my favorite synergy of all time. First take the LSD, then take a comfortable dose of banisteriopsis caapi tea, then smoke as much DMT/Changa as you desire. Absolutely astonishing.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Mushrooms|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A lot of people don't like this combination for some reason- both drugs are just so powerful they may not need to go together, with that said however some people like the combo and it is OK to take.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy with Psilocybe mushrooms.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|I took the Mushrooms while coming down from the LSD and I didn't feel any effect whatsoever. (EDIT: You probably have to take lots of Shrooms to fight the tollerance)}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I haven't experimented enough with this combination to say for sure. Only very small doses, and they were kind of hazy.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Classic Combo. Take at the same time or let the acid kick in then take the MDMA. Profound synergy!}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDMA gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|MDMA and LSD together is one of the most amazing synergy in terms of dancefloor experience...}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|The only time I did it, I took the LSD a while after the MDMA. Everything was very smooth and shiny. Great dancing combo!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|&lt;br /&gt;
MDMA removes any negative experiences I feel with LSD. POWERFULLY beautiful combination! All aesthetics are increased 10x, music is beautiful and flowing, playing music is amazing, dancing is amazing. Cuddling, hugging, telling people you love them... yes, this is a winner.}}&lt;br /&gt;
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==== LSD + MDAI ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDAI|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDAI gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Mescaline ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy but it's hard to tell how each drug is affecting each other. A bit like LSD + MDMA but a deeper, so to speak.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Cannabis vasodilates the vasoconstriction of LSD especially if taken orally. Potentiates and smooths out the trip. Great for daily smokers. Has been known to cause anxiety in those who don't use Cannabis too often.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|I almost never use [[cannabis]], I wanted to use the cannabis versus the stimulation of the LSD. It gave me more visuals but it also made me dizzy. Overall I did not like it.}}&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|Definitely has led to a bunch of paranoia at times (I'm prone to that with weed alone though) but if combined carefully it can be totally worth it although i never do it anymore (no lsd). If a large amount is smoked at the peak-especially if i have a low tolerance- then it can really catapult the experience into a sort of out of body type thing with full blown 3-d immerse visions, IME}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|It gives a bit of anxiety, although the effect of LSD is potentiated for a little while. Be aware, it's very hard to roll a spliff while tripping }}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Cannabis + Tobacco====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I mostly smoke spliffs, but I find spliffs (a 50/50 mix of cannabis and tobacco) To be quite pleasant at all periods of the LSD comeup. Usually my physical form is quite shakey and or cold during the LSD comeup, and cannabis warms me up and calms down any tension or shakiness. Spliffs induce a deep trance state for me, very pleasant.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + MXE ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Aetherius Rimor|[[Image:Negative.png]]|Did 30mg of [[MXE]] in the 2nd hour of 2 hits. That's the only time I've not been at home and unable to verbalize/coordinate movement. Luckily that's what designated drivers are for! Won't combine them again. Definitely stronger effects than same dose of each independent of each other.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The MXE potentiates the [[LSD]] effects with more visuals but it also significantly alters motor function to the point of immobility at high doses.}}&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Radical and profound potentiation/synergy. 12+ hour trip and much longer to sleep. I really love the synergy of LSD+MXE but I'm the kind of person who naturally chills during a trip, so being pancaked by effects is just an extra plus for me.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|I have tried this combination many times, but only at high doses of MXE, I loved this combination, it intensified and increased the depth and power of the dissociated 'hole' while making it easier to bring back more from the experience. The only negative effects Ive felt is the dissociated 'whobblies' that last for an hour or two after the hole, which can be annoying while trying walk around on LSD. In my experience, it is best taken early in the LSD trip, when the effects subside you are usually at the LSD peak, this also seems to ease any anxiety. (I would also like to mention I am quite mobile at high doses of MXE while on LSD, only after mobility can be hindered by the drunken like 'whobblies')}}&lt;br /&gt;
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==== LSD + Amphetamines ====&lt;br /&gt;
{{SubstanceInteraction|LSD + Amphetamines|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:neutral.png]]|Somewhat safe but...Makes the LSD less visual and a bit more difficult to handle mentally because of the stress caused by the stimulants. It can be an interesting mix if partying but I would try to avoid it if possible. At least try to get pharmaceutical grade stimulants and not dirty street pills.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Harmalas (MAOI)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|You MUST make sure you have pure LSD, however! You do not want to mix harmala (RIMA, MAOI) with an unknown drug laid on blotter. It's great taken with a dose or taken after the dose has kicked in, as the vasodilation of the harmala counters the vasoconstriction of the LSD.}}&lt;br /&gt;
{{UserDescription|Enoon|[[Image:Neutral.png]]|Super strong synergy, stronger than usual visuals, visions, OBE, but also nausea, imobility and substatial amount of apprehension}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy/potentiation, first timers should take very small doses to see how they react and only raise gradually.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I must admit I'm a bit of a Harmala &amp;quot;fiend&amp;quot;. I love them and I see no negative applications to them, pretty much, as long as you are physically safe. They potentiate the visuals of LSD, get rid of the shakes and nervousness, help me emotionally sort through things and make me warm and content and happy. This is a WINNING combination, especially with chocolate caffeine or spliffs. all very good in my books. Great for meditation, dancing, writing, drawing, or playing music.}}&lt;br /&gt;
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==== LSD + Amanita Muscaria/Pantherina ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Amanita Muscaria/Pantherina|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Great synergy, tends to make the trip more challenging and more visionnary, more entheogenic also, but it is again harder than LSD on it's own.}}&lt;br /&gt;
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==== LSD + Alcohol====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mescaline|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|Doesn't make sense to me to combine a CNS depressant with the brilliant effects of LSD.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Great and jolly, but it makes the trip a bit blurry and less powerful. Don't over do it, your liver wont appreciate it!.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't enjoy alcohol in general, so I'm slightly bias. When I was younger (15-16) I would shotgun beers on LSD and that was quite nice, but any hard alcohol combined with LSD turns you into a flailing, falling idiot apologizing for making such a big mess.}}&lt;br /&gt;
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==== LSD + GHB====&lt;br /&gt;
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{{SubstanceInteraction|LSD + GHB|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't have enough concrete experience with this combination, but I haven't experienced negative interactions the few times I have done them. the GHB is very warm and mellow, although a bit of nausea or headache or spinny-ness can occur at higher doses, if everything is kept moderate it is much more pleasant than alcohol, although not quite as pleasant as MDMA.}}&lt;br /&gt;
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=== Mescaline ===&lt;br /&gt;
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&lt;br /&gt;
Mescaline is a phenethylamine that does not have an amphetamine group on the molecule, unlike MDMA. This allows it to be able to be used with harmalas without contraindication. A very gentle and long lasting psychedelic with great empathic and stimulating properties. &lt;br /&gt;
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==== Mescaline + Caffeine ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A great way to potentiate your mescaline dose is with caffeine, especially coffee. Yerba mate and other teas are good too. Even the days after a trip, a nice cup gets you right back in that lovely state-of-mind. Some may find this combo too stimulating, however. The coffee can also be used to get digestion flowing if you are having indigestion from the cactus.}}&lt;br /&gt;
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==== Mescaline + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Noticeable potentiation and takes the edge off the stimulation subsequently. These two go hand-in-hand if you are a regular cannabis user. If not, start low!}}&lt;br /&gt;
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==== Mescaline + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Harmala|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|No contraindication here. A nice synergy. The harmala takes away some of the stimulation of the mescaline and makes the experience more dreamy. }}&lt;br /&gt;
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==== Mescaline + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|You can drink a lot of alcohol on mescaline, but I don't see the point. Takes away from the profound effects of the psychedelic.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|In high doses it's extremely confusing! Good chances to blackout and puke. }}&lt;br /&gt;
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==== Mescaline + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Nice combo, but it wasn't enough to understand its effects.}}&lt;br /&gt;
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=== Iboga ===&lt;br /&gt;
&lt;br /&gt;
Careful with this one! Much research and tests must be done before ingesting this substance. It is clinically proven to slow down a rhythm of the heart beat and has killed people because of this. A heart panel and EKG are common tests preformed before ingesting this substance. Please beware of this and do a lot of research before even considering this very profound medicine! Side effects include disorientation, immobility, nausea, in high doses for very long periods of time. Some people still can't drive a car 1 week after a flood dose, for example.&lt;br /&gt;
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==== Iboga + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|LSD becomes much more potent after Iboga and I would suggest taking it sometime between 1-7 days after taking a low dose of Iboga. For me I find that the LSD really puts the teachings of the Iboga into perspective. Be careful though, there is a definite potentiation.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:negative.png]]|very challenging in my experience so the LSD was probably very high (vial wash) with loads of noribogaine (2 grams RB every days for four to five days) in the system. I personnally wouldn't recommend it.}}&lt;br /&gt;
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==== Iboga + Mushrooms ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I find that psilocybe mushrooms are a really great synergy. They seem to kick in the Iboga about 3x as hard, so a low dose of both makes for a good journey. Euphoric, meditative, deep combination. Great for sorting things out in your life.}}&lt;br /&gt;
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==== Iboga + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with Iboga and cannabis. Noticeable potentiation. Also takes care of the intense nausea with higher doses of Iboga a bit. I believe this synergy is even used traditionally in some instances.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Iboga and canabis are great together, the iboga focus the train of thought from canabis while canabis relax the iboga (stimulant at low doses) experience.}}&lt;br /&gt;
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==== Iboga + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Harmala|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|While myself and others have found a low dose of harmala to be a nice synergy with Iboga, others have found the combination too intense. Start low and work your way up.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:positive.png]]|Iboga and harmalas must be treaten with caution though in low doses, it seems like a very good combo though questionnably safe (in regards of mixing RIMA and SSRI).}}&lt;br /&gt;
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==== Iboga + Coffee ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Coffee|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love a low dose of Iboga with a good cup of coffee, and cannabis. I find it stimulating both physically and with the clarity of mind. Some may find this too stimulating. Don't expect to sleep the night of taking this combo!}}&lt;br /&gt;
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=== MDMA ===&lt;br /&gt;
&lt;br /&gt;
The most common side effects of MDMA are jaw tension, feeling burnt-out the next day, and it's minimal amount of neurotoxicity.&lt;br /&gt;
A lot of people &amp;quot;pre load&amp;quot; with substances that are neuroprotectant before, during, and after the experience. Neuroprotectants include cannabis, nootropics, vitamin C, 5-HTP, and others. Jaw tension can be countered again with transdermal magnesium, conscious relaxation, meditation and massage. As for feeling burnt-out, try to only redose a small amount one time or not at all. Constantly redosing can cause more burnout srensations. Also dosing too high. You might want to touch, hug, kiss, and tell how much you love everything around you, too.&lt;br /&gt;
  &lt;br /&gt;
Taking MDMA with MAOI and certain prescription medications can lead to seratonin syndrome and even death so plesse be careful!&lt;br /&gt;
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==== MDMA + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + Harmalas (MAOI)|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with MDMA and cannabis. Smooths out the stimulation. Biologically speaking, the cannabis actually works as a neuroprotectant against the neurotoxicity of MDMA. They go hand-in-hand if you are a fan of cannabis!}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Very nice, but you end up smoking way too much.}}&lt;br /&gt;
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==== MDMA + LSD + Ketamine + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + LSD + Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Better than OK for me. Have had some of the best nights of my life with this cocktail.}}&lt;br /&gt;
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==== MDMA + DMT + Ketamine ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + DMT + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Out-of-this-world OEVisuals. The euphoria of the MDMA is present and the visual quality of the K synergizes with the DMT in a very strange way. I would suggest taking only small dosages with all of those three if you are to give this combo a try.}}&lt;br /&gt;
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=== Ketamine ===&lt;br /&gt;
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==== Ketamine + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is a pretty classic and noteable synergy that many people love. The K takes you very deep into yourself, and away from yourself at the same time.}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. Similar to the 2CB combo, be careful, both of these drugs have a tendency to be a bit mind bending, and in combo, expect it to get wild!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|LSD + Ketamine is definitely a strange combination. In my experience it lends itself to meditation because alot of the time the mind is too befuddled to properly draw a train of thought. I find this combination quite inarticulating, it's one of the few drug interactions that make me a bit of a &amp;quot;dumbass&amp;quot;, and just puddle me on the floor. Lower doses of ketamine + lsd are good for dancing, higher doses, for trancing.}}&lt;br /&gt;
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==== Ketamine + LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Love it!}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. You will get lost in the deepest recesses of your mind for quite some time, I love comatose tripping, but it isn't for everyone.}}&lt;br /&gt;
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==== Ketamine + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Harmala|#604040|#FF6060|BAD IDEA!|Harmalas are contraindicated with dissociatives, this means you do not want to combine them. At high doses the cardiovascular system can shut down.|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|Made the mistake of trying changa on top of LSD + K once and I will never do that again. Intense bronchial constriction and chest pain was noted.}}&lt;br /&gt;
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==== Ketamine + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coming back from the ketamine trance and smoking cannabis. Great for meditation and integration if you enjoy cannabis!}}&lt;br /&gt;
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==== Ketamine + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|DMT on Ketamine is out of this world stellar. The dissociative properties of ketamine completely eliminate any anxiety present, and the two work together to take you deep into whatever it is that we are...}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Some people suggest ketamine may smooth the entry int tryptamine space and some report incredible experiences. Special care is needed with ketamine due to it's potentially addictive nature and due to being dissociative/anaesthetic and increased risks of physical accidents. Justin Case's best results have been reported when k dose is kept low and tryptamine dose is solid but not excessive.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|This combination is grandeur, extremely powerful. I agree with both House and Endlessness, especially about the addictive part. Extensive use of the this combination and other DMT + Dissociatives, seems to make a preexisting addiction worse. It's a lot of strain on ones psyche to abuse this combo.) }} &lt;br /&gt;
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==== Ketamine + LSD + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Throwing DMT into the mix is just that much more powerful.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|^ What House said.}}&lt;br /&gt;
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==== Ketamine + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Some people love it, I don't. I don't like small bumps of K, so when I take it, it always end up taking over all the rest.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Ketamine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|I heard it's not very safe. I did it few times and the day after I always felt miserable.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Salvia Divinorum===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|OK. can be extremely disturbing though or unbelievably profound and real.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + Changa + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Changa + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is probably my favorite mix. I've had some of my deepest experiences mixing these three including one with multiple breakthroughs one on top of the other cascading deeper with a new universe created and destroyed each time.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is a very therapeutic anesthetic. This kills pain very well and leaves me in a dreamy visionary state without the mind warping dissociating effects that salvia has on its own. As long as you don't go heavy on the salvia! }}&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good! Great way to take the edge off of the pre-flight anxiety for salvia, which can be pretty rough at times.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Effects are dramatic but its not clear if there is synergy or more like additive effects. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== RC's ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 2C-B ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== 2C-B + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-B + Ketamine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Have seen 2 people lose the plot on this combo, so be careful. For me, it subdues the edginess of the phenethylamine buzz, while adding a trippy colourful edge to the Ketamine. Can get confusing, which I think was why people freaked out a bit.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + 2CB + K + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + 2CB + K + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Similar to the above, moar euphoria, but again please be careful with dosages.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 2C-I ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== 2C-I + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-I + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:negative.png]]|made me feel sick, smoking anything on 2CI wasn't nice.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== MXE ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MXE + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MXE + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. deep, visual, introspective, make sure you don't have anything to do / people to entertain as chances are you will be lost in thought. Did experience a little muscle tremoring, but less than 2CI on its own.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== 5-MeO-DALT + MXE ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|5-MeO-DALT + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|While on ~50mg 5-MeO-DALT orally I did a little test bump of 15 mg MXE insufflated and within minutes felt my heart rate go up and felt very dizzy. Thought that I had finally done it and mixed the wrong stuff and I would have to go to the ER but it stopped escalating and I just waited it out.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 25i-NBOMe ===&lt;br /&gt;
&lt;br /&gt;
==== 25i-NBOMe + Cannabis + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|25i-NBOMe + Cannabis + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|billydgator|[[Image:Positive.png]]|Awesome! About 2.5 hours into an 25i nbome trip i took some small blasts of spice, brought me from ++ to ++++.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== AM-2201 ===&lt;br /&gt;
&lt;br /&gt;
==== AM-2201 + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|AM-2201 + MDMA|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Negative.png]]|Can be VERY hallucinogenic, only smoke a little! Bizarre and realistic and gory hallucinations (man with half a leg bleeding allover the place!) are possible, voices become distorted and merged and speak impossible ridiculous things. The hallucination is short lived.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== MDAI ===&lt;br /&gt;
&lt;br /&gt;
==== MDAI + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDAI + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized hits of DMT seem harder to break through on, but the effect of the DMT seem prolonged. Strange visuals (small pinpoint kaleidoscope patters appear and dissappear), last for longer than the spice effects would last, by up to 25 minutes longer. Does not seem dangerous, but the fact it makes open eye visuals linger for so long is interesting...}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Medicine ==&lt;br /&gt;
&lt;br /&gt;
=== SSRI/SSRE ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Cannabis ===&lt;br /&gt;
&lt;br /&gt;
Cannabis works as a potent anti-inflammatory and vasodilating medication. Those who use it often find that it goes well with almost every other drug, while those who seldom use it may find that when combined with psychedelic substances it can cause paranoia and uncomfortable potentiation. If you are unfamiliar with the ways cannabis synergizes with other substances, it is wise to start low and work your way up to a comfortable amount. Many find that oral cannabinoids act as a more potent vasodilator than smoked, making this a good option for countering the vasoconstriction of drugs like LSD and LSA. Many people also use cannabis to counter the nausea caused by other drugs. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Cannabis + Harmalas (MAOI) ====&lt;br /&gt;
{{SubstanceInteraction|Cannabis + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:positive.png]]|Harmalas potentiate the effects of cannabis, adding a nice dreamy feel and tracers to the vision. Since they are both vasodilating compounds, some people experience headaches if combined in high doses. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Other ==&lt;br /&gt;
&lt;br /&gt;
=== Nootropics/Piracetam/Aniracetam ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Piracetam + Psychedelics/Amphetamines ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Piracetam + Psychedelics/Amphetamines|#805000|#E0A040|OK but|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Trout notes that justin case, toad and others have reported substantial increase in potency of phenetylamines (such as MDMA, mescaline, amphetamines) and suggest dosage is halved. Possible potentiation of tryptamines too. There is very little data on the pharmacodynamics and toxicity of this mixture, so care is adviced, even though due to low toxicity of tryptamines and piracetam by itself, its possible the toxicity of mixture is also low.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== LSD + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I have been dosing piracetam daily for a few weeks now, and in that time I've done LSD twice. Definitely noticed that each time the piracetam VASTLY improves ability to articulate myself, ability to recall the trip and get into deeper meditative states. Piracetam also greatly helps my ability to write more clearly in my journals, improves my ability to play music and LSD enhances my musical creativity. All in all, very good combination.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Caffeine + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Caffeine + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dream Weaver|[[Image:Positive.png]]|I occasionally dose piracetam anywhere from 800mg to 4 grams ingested on an empty stomach (dissolved in water). I find the synergy of caffeine + piracetam to be quite soothing. It is important not to ingest too much caffeine or an anxiety like feeling will occur/stomach problems... Mostly positive if done right. Effects are very soothing and uplifting. Make the most mundane task entertaining. You become quick and sharp as a whip. Effects are somewhat similar to 30mg xr adderall + 5-15mg valium (Note: Do not mix adderall and valium). Caffeine + Piracetam is a great combo! Ideal for mornings!}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Kava Kava ===&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava kava is relaxing and aids in dissipating pre-flight anxiety. A warm cup is great after DMT insufflation or vaporization. There is a noticeable synergy between the two and no discomfort or side effects have been noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + LSD ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava Kava after the peak of LSD when it's wearing off is a great way to take the edge off and get some rest. It's very effective and enjoyable this way with no side effects noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy. Very relaxing.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== DXM ===&lt;br /&gt;
&lt;br /&gt;
==== DXM + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|Great. Visually incredible. Cannabis at peak enhanced visuals even further. Use more mushrooms than DXM.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DXM + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good. Great way to up the psychedelic aspect of dex.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Tobacco ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Great. Dex really makes tobacco shine, brings out the best world of nicotiana.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + N2O ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + N2O|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Very, Very intense. Too much for some people, but for others, euphoria.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + HBWR (LSA) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + HBWR(LSA)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|It really increases the psychedelia of dex, brings some awesomely colorful visions, but be very careful. Not much is known about the interactions of these two. I would not go above 3 HBWR seeds in combo.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + DMT ====&lt;br /&gt;
{{SubstanceInteraction|DXM + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|One of the most intense experiences I could possibly imagine. Classic Dissociative + DMT, but incomparable at the same time, I could say I like this combination better then DMT + Ketamine, or DMT + MXE, but its incomparable.  It dissolves any preflight, or during anxiety whatsoever, the utterly intense godly power of DMT is given to YOU. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Chocolate/Theobromine ===&lt;br /&gt;
&lt;br /&gt;
Theobromine, a methylated xanthine found in chocolate and yerba mate, is a stimulant and psychedelic potentiator.&lt;br /&gt;
&lt;br /&gt;
Low doses combined with psychedelics causes noticeable potentiation and empathy.&lt;br /&gt;
High doses have the potential to cause nausea and over stimulation, so start low and work up to a comfortable dose!&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Aka The Mocha. Nice warm fuzzy sociable synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Definite potentiation and synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Passionflower ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Passion Flower|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:neutral.png]]|OK, but don't use a lot of theobromine. I have had psychedelic effects with this combination, but also intense nausea and bronchial-constriction at higher doses.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK but do not use a lot of theobromine or harmala. A little goes a long way! Same thing goes here if you have a little too much of either theobromine or harmala expect nausea and vomiting. At appropriate doses however the synergy is very nice. Theobromine potentiates the harmalas and any psychedelics you take as well.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I haven't experimented too heavily with eating cacao on LSD, but I usually eat one or two handfulls of raw cacao nibs. I found the stimulation synergistic, very good for walking or running through the forest. I found that the cacao gets rid of the &amp;quot;shivers&amp;quot; I experience from LSD and warms me from the inside.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Bufotenine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Bufotenine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Entheogenerator|[[Image:Positive.png]]|I typically predose pure theobromine about 20-30 minutes before smoking bufotenine. Theobromine is a natural vasodilator and can be used to counteract the unpleasant physical effects of bufotenine caused by vasoconstriction. It may not eliminate the discomfort completely, but in my experience the theobromine powder has reduced the vasoconstriction to a more tolerable level. Raw cacao could probably be used to the same effect, but I have not tried. Ginger can be added to the mix to reduce nausea.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Kratom ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kratom + MXE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kratom + MXE|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Effects: Like 10-15 mgs of Hydrocodone.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== N2O ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== N2O + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|N2O + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|N2O at peak of a mescaline trip was incredibly euphoric. Felt like psychedelic MDMA.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== N2O + DMT ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|N2O + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|When nitrous is inhaled immediately after dmt, its reported by some people to significantly enhance the experience.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== N2O + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|N2O + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|OK. Very powerful. Be prepared to lie down and be somewhat paralyzed, depending on dosage.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== N2O + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|N2O + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Amazing visuals. Out of body experience, very comfortable but no contact at all with the body.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== N2O + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|N2O + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Amazing! For few minutes you are in a DMT like world. (I'd love to try LSD + N2O)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Alcohol (Ethanol) ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:neutral.png]]|I have done this a few times and been safe, but I was very careful and spaced my drinks out. I have read horror reports of people drinking to much on dex, and puking for upwards of an hour or two.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Negative.png]]|Puke city.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:negative.png]]|Another potential Show Stopper. The Alcohol really tends to lessen, dull, or end the effects of the mdma. Aside from that, there is the danger of dehydration--when you are rolling you should drink water.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Quite nice, but do not over do it! If you have been drinking too much, you'll be hit by a train when the MDMA comes down.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Bufotenine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Bufotenine + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Not a good combo. The Bufotenin's nausea will probably make you puke and the Alcohol will diminish the Bufotenin visual effects.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Caffeine ===&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Caffeine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|Not so good. Caffeine disturbs the mushroom flow.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coffee or yerba mate with LSD. Wonderful combo.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I'm a bit of a coffee / mate junkie, so I find the combination quite synergistic. Smoking a spliff and drinking coffee on LSD makes me feel like all is right in the world and I can sit in meditation and take a good 30 minutes to drink my coffee and have my smoke. It lends itself to visual enhancement and incredible tingling sensations in the body, which for some people could make them quite restless, but I enjoy meditation on stimulants.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Melatonin ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Melatonin + Mushrooms + Harmala + Cannabis + Changa ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Melatonin + Mushrooms + Harmala + Cannabis + Changa|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|50-100mg melatonin (very meditative and harmala-esque for me. Combines well with others like a mind lube. A few hours later - lower dose of oral harmalas (preferably caapi) + mushrooms + smoked Cannabis + changa to top it off and push it all through. Amazing synergy. Need to balance the ratios accordingly though. You can leave out the melatonin if your not used to higher doses (they're not really that sleepy like the lower doses though, oddly). I prefer this combo after a day or to without sleep. Sleep deprivation is a powerful means of accessing altered states that's been used for thousands of years, like in the epic of Gilgamesh, for example. That's not for everyone though and works best with a raw, plant based diet.)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Benzos/Barbituates ===&lt;br /&gt;
&lt;br /&gt;
Benzodiazepines can be reduce an agitated rough/unpleasant trip but are generally not recommended if other non-invasive supportive care-taking can be done, because these substances will dull the consciousness and might prevent the tripper from learning from the hard experience and integrating it.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Chlorpromazine + Psychedelics ====&lt;br /&gt;
{{SubstanceInteraction|Chlorpromazine + Psychedelics|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:neutral.png]]|Chlorpromazine substantially diminishes the effects of DMT, LSD and other similar molecules (see Moore et al 1975, Shah &amp;amp; Hedden 1978}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=29012 'Known drug-interactions' Wiki page]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Harm reduction]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Lextek</id>
		<title>Lextek</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Lextek"/>
				<updated>2013-11-30T00:12:44Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Part 5: Defat Step 1: Acid Wash */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{ShowInfo|[[Image:Note_error.png]]|'''Note:'''|This page is a transcription of Lextek&amp;lt;ref&amp;gt;Lex's DMT Extraction v1.0 Oct. -2007[http://wiki.dmt-nexus.me/Image:Lextek_v1.pdf]&amp;lt;/ref&amp;gt;. The content is to remain accurate as such.}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{ShowInfo|[[Image:Note_error.png]]|'''Warning:'''|DO NOT USE THIS TEK FOR ACACIA EXTRACTION!.}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Section 1: Extraction of DMT ==&lt;br /&gt;
&lt;br /&gt;
=== Materials needed ===&lt;br /&gt;
(Quantities can be scaled accordingly to work with smaller or larger amounts of material)&lt;br /&gt;
* 2 kilograms of DMT containing plant material (Acacia Obtusifolia bark will be used here)&lt;br /&gt;
* 250 grams of Sodium Hydroxide (Caustic Soda / Lye) – Bunnings / Safeway&lt;br /&gt;
* 1 Litre of white vinegar (dilute Acetic Acid) – Safeway&lt;br /&gt;
* 2 Litres of Shellite (non-polar solvent) – Bunnings&lt;br /&gt;
* 12 Litres of distilled water (polar solvent) – Bunnings&lt;br /&gt;
&lt;br /&gt;
The idea behind the extraction is that DMT is in the plant; we can get it out.&lt;br /&gt;
&lt;br /&gt;
At our advantage, the state of the DMT can be changed between a salt or freebase by using acids or bases respectively, ie: if you have a pH 4 (acidic) solution containing DMT, the DMT will be converted to a salt (using acetic acid: DMT Acetate, using tartaric acid: DMT Tartrate, etc..) If you now basify this to pH 14, all the DMT salt will be converted to its freebase form.&lt;br /&gt;
&lt;br /&gt;
As we change the state of the DMT, we also change its solubility properties:&lt;br /&gt;
* DMT salts are soluble in polar solvents (water, alcohol) but insoluble in non-polar solvents.&lt;br /&gt;
* DMT freebase is soluble in non-polar solvents (Shellite) but is insoluble in polar solvents.&lt;br /&gt;
&lt;br /&gt;
Understanding these basic points allows an extraction technique to be devised:&lt;br /&gt;
# '''Prepare Your Bark''' &amp;lt;br&amp;gt; Chop up and grind your bark to maximise its exposed surface area.&lt;br /&gt;
# '''Acid Cook''' &amp;lt;br&amp;gt; Simmer the bark in pH 4 acidic water (using vinegar). Keep the liquid and discard the bark. &amp;lt;br&amp;gt; The low pH ensures all DMT is in its salt form, which will dissolve into the water.&lt;br /&gt;
# '''Basify''' &amp;lt;br&amp;gt; Basify the liquid to pH 14 with Sodium Hydroxide (Caustic Soda / Lye). &amp;lt;br&amp;gt; The high pH ensures all DMT is in its freebase form, which is soluble in Shellite.&lt;br /&gt;
# '''Initial Shellite Extraction''' Add an amount of Shellite to the above solution, shake, separate, and repeat. &amp;lt;br&amp;gt; The freebase DMT will dissolve into the Shellite, along with some unwanted plant gunk.&lt;br /&gt;
# '''Defat Step 1: Acid Wash''' &amp;lt;br&amp;gt;  Acidify water to pH 4 using acetic acid (vinegar) and add to the combined Shellite extractions. &amp;lt;br&amp;gt; This will convert the DMT freebase to the water-soluble salt, DMT Acetate. &amp;lt;br&amp;gt; The DMT Acetate will move from the Shellite to the water leaving behind the plant gunk.&lt;br /&gt;
# '''Defat Step 2: Basify''' &amp;lt;br&amp;gt; To the water + DMT Acetate solution, add an amount of Sodium Hydroxide. &amp;lt;br&amp;gt; This will again convert the DMT to its freebase form, which is soluble in Shellite.&lt;br /&gt;
# '''Final Shellite Extraction''' &amp;lt;br&amp;gt; Add an amount of Shellite to the above solution, shake, separate, and repeat. &amp;lt;br&amp;gt; The freebase DMT will dissolve into the Shellite. At this point no plant gunk remains.&lt;br /&gt;
# '''Freeze Precipitation''' &amp;lt;br&amp;gt; The last step is to get your DMT freebase out of the Shellite. &amp;lt;br&amp;gt; At freezing temperatures, the DMT becomes insoluble in Shellite and will precipitate out.&lt;br /&gt;
&lt;br /&gt;
== Step-by-step guide ==&lt;br /&gt;
&lt;br /&gt;
=== Part 1: Prepare Your Bark ===&lt;br /&gt;
Preparing the bark is a crucial step to ensure your yield is as high as possible. The aim is to maximise the surface area of the bark so the majority of the DMT is exposed and not protected inside thick layers of wood.&lt;br /&gt;
&lt;br /&gt;
I have tried many methods and I find this one to work at least. Some methods are better than others; its personal choice so be innovative and find the one that works best for you.&lt;br /&gt;
# Weight an amount of bark, for this extraction 2 kilos will be used.&lt;br /&gt;
# Using secateurs chop the bark into pieces no larger than pictured here - the smaller the better.&lt;br /&gt;
# Fill your grinder to about a third of its capacity with bark and grind.&lt;br /&gt;
# Shaking it around while grinding helps to ensure that most of the bark comes into contact with the blades.&lt;br /&gt;
# Do this until all your bark is powdered (or as close as possible to).&lt;br /&gt;
# Be sure to give your grinder a rest between loads if you can feel it heating up too much.&lt;br /&gt;
&lt;br /&gt;
=== Part 2: Acid Cook ===&lt;br /&gt;
The acid cook will convert the DMT into its water-soluble acetate salt (acetate as we are using vinegar – acetic acid). The DMT Acetate will migrate away from the bark, into the acidic water.&lt;br /&gt;
&lt;br /&gt;
Most acids can be used without a problem. We will use white vinegar (which contains roughly 5% acetic acid) diluted in distilled water. It is easy to get and fairly safe to work with.&lt;br /&gt;
# Acidify an excess amount of distilled water by mixing one part vinegar to three parts water. You are aiming for a '''pH of 4'''. &amp;lt;br&amp;gt; Use a digital pH meter or litmus paper to determine the pH of the solution.&lt;br /&gt;
# Place all the bark into a large saucepan and fill with the acidified water, ensuring all the bark is well covered. Four litres per cook was used here. &amp;lt;br&amp;gt; Bring the mixture to a light simmer and proceed to cook for a further hour. &amp;lt;br&amp;gt; Once complete, pour off and save the liquid. Perform this step a further two times.&lt;br /&gt;
# Combine all liquids and filter out the fine bark particles through a muslin cloth. &lt;br /&gt;
# Reduce all liquids down to a few liters on low heat. This may take several hours. &amp;lt;br&amp;gt; For your own sake '''BE SURE''' that your kitchen has adequate ventilation. Humidity can build up quicker than you think and before you know it your ceiling and walls may be dripping in oily red acidic liquid !!&lt;br /&gt;
&lt;br /&gt;
=== Part 3: Basify ===&lt;br /&gt;
Basifying the acidic solution to pH 14 with Sodium Hydroxide will convert the DMT Acetate to the DMT base.&lt;br /&gt;
&lt;br /&gt;
The DMT base is insoluble in polar solvents (water) but soluble in non-polar solvents (Shellite).&lt;br /&gt;
&lt;br /&gt;
Performing this conversion is preparation for Part 4: Initial Shellite Extraction &lt;br /&gt;
# Let the reduced acidic solution cool to lukewarm and pour into a HDPE jug like the one the water came in.&lt;br /&gt;
# Weigh 100 grams of Sodium Hydroxide and '''SLOWLY''' add 10 grams at a time, shaking well each time. This will raise the '''pH to 14'''. &amp;lt;br&amp;gt; The solution will turn black. &amp;lt;br&amp;gt; Use a digital pH meter or litmus paper to determine the pH of the solution. &amp;lt;br&amp;gt; '''NOTE:''' Adding base to water is an exothermic reaction (releases heat) and if added too quickly to already hot water, spitting can occur. &amp;lt;br&amp;gt; You DO NOT want this stuff on you !! &amp;lt;br&amp;gt; Once the solution is basified and stable, swirl it around to homogenise the mixture.&lt;br /&gt;
 &lt;br /&gt;
=== Part 4: Initial Shellite Extraction ===&lt;br /&gt;
Shellite is a non-polar solvent and can be used to remove non-polar substances (DMT base) from polar solutions (water).&lt;br /&gt;
&lt;br /&gt;
'''Note:''' This step must be done while the solution is HOT to maximise the solubility of the DMT base into the Shellite. Without heat, yields will be greatly reduced.&lt;br /&gt;
# Pour 250mL of Shellite into the basified solution. Put the lid on and shake. &amp;lt;br&amp;gt; '''NOTE!!''' The first few shakes will cause a rapid release of vapors which must be released. Watch the pressure carefully and release frequently !! &amp;lt;br&amp;gt; '''Adequate ventilation is a must at this point'''&lt;br /&gt;
# Let the mixture sit for a few minutes. Looking closely you will see two layers. &amp;lt;br&amp;gt; The top layer is the Shellite layer which now contains the DMT base and some fats and oils from the bark.&lt;br /&gt;
# Using a siphon device or some other method, separate top non-polar layer from the bottom polar layer. &amp;lt;br&amp;gt; Experiment with different ways to do this (turkey baster, ghetto separatory funnel, etc..) and find one that works for you. &amp;lt;br&amp;gt; I find siphoning the bottom layer to another jug allows for good separation.&lt;br /&gt;
# Repeat steps 2 and 3 another two times and combine the Shellite pulls. For the third pull use 500mL of Shellite. &amp;lt;br&amp;gt; Remember to ensure that both the solution and Shellite are HOT to aid in the extraction. Use a hot water bath for this. &amp;lt;br&amp;gt; '''DO NOT''' use an open-flame heat source !!! &amp;lt;br&amp;gt; For the third pull, add another 50 grams of Sodium Hydroxide to the solution before extracting and shake real well, this will heat the solution significantly.&lt;br /&gt;
 &lt;br /&gt;
=== Part 5: Defat Step 1: Acid Wash ===&lt;br /&gt;
As the Shellite solution pictured above contains both DMT base and plant gunk, we are now going to remove the DMT from the solution and leave the plant gunk behind.&lt;br /&gt;
&lt;br /&gt;
This will be done by washing the Shellite + DMT + plant gunk solution with acidic water, resulting in the DMT base once again becoming the water-soluble salt, DMT Acetate and migrating away from the Shellite, however leaving behind the plant gunk. &lt;br /&gt;
# Again, acidify an excess amount of distilled water by mixing one part vinegar to three parts water. You are aiming for a '''pH of 4'''. &amp;lt;br&amp;gt; Use a digital pH meter or litmus paper to determine the pH of the solution. &lt;br /&gt;
# Add approximately 250mL of acidic water to the Shellite solution. The mixture does not need to be hot; in fact it is better if all liquids at this step are kept at room temperature as otherwise plant gunk will come back across. &lt;br /&gt;
# Using the same siphoning method in Part 4 - Step 3, siphon off the top non-polar layer from the bottom polar layer, this time keeping the polar layer (acidic water).&lt;br /&gt;
# Repeat step 2 three more times and combine the three polar layers. &amp;lt;br&amp;gt;For the third time use 500mL.&lt;br /&gt;
&lt;br /&gt;
=== Part 6: Defat Step 2: Basify ===&lt;br /&gt;
Once again, in preparation to extract the DMT from the acidic water solution, we are going to basify the liquid.&lt;br /&gt;
&lt;br /&gt;
This will again convert the water-soluble DMT Acetate salt into the water-insoluble DMT base. Note that no plant gunk exists in the vinegar solution; the solution at this point consists only of acidic water + DMT Acetate.&lt;br /&gt;
&lt;br /&gt;
Slowly add 60 grams of Sodium Hydroxide to the solution to raise the '''pH to 14'''.&lt;br /&gt;
&lt;br /&gt;
Use a digital pH meter or litmus paper to determine the pH of the solution.&lt;br /&gt;
&lt;br /&gt;
Note that the solution has been placed into a new vessel.&lt;br /&gt;
&lt;br /&gt;
=== Part 7: Final Shellite Extraction ===&lt;br /&gt;
We will now extract the DMT base from the basified solution with Shellite.&lt;br /&gt;
&lt;br /&gt;
As previously explained, adding Sodium Hydroxide (base) to the acidic water + DMT Acetate solution converted the DMT Acetate salt to the DMT Base which is insoluble in our polar solvent (water) and soluble in our non-polar solvent (Shellite). &lt;br /&gt;
# Measure 250mL of Shellite and add it to the acidic water. &amp;lt;br&amp;gt; Heat the mixture in a hot water bath and shake.&lt;br /&gt;
# Allow the layers to separate and siphon and separate, keeping the non-polar layer this time. &amp;lt;br&amp;gt; Repeat step 1 two more times and combine the Shellite extractions. &amp;lt;br&amp;gt; Again, for the third pull add another 30 grams of Sodium Hydroxide (to reheat) and extract with 500mL of Shellite.&lt;br /&gt;
&lt;br /&gt;
=== Part 8: Freeze Precipitation ===&lt;br /&gt;
Our solution is now clean enough to proceed to removing the DMT Base from the Shellite.&lt;br /&gt;
&lt;br /&gt;
# Pour the solution into a wide-mouthed jar that you can fit your hand into and with the use of a fan, evaporate approximately half of the solution. &amp;lt;br&amp;gt; You may notice that your solution has turned milky and an oily film has formed on the glass where the solvent has been evaporated. This is actually a bunch un-crystallised DMT. If you want to get your efficiency right up then heat up the solution with a hot water bath and swirl it around plenty to re- dissolve all this DMT.&lt;br /&gt;
# Place the solution in the freezer and resist all temptation to disturb it for at least 48 hours.&lt;br /&gt;
# After 48 hours or more, pour off the Shellite being careful not to lose any DMT floaters with it. You should see something like this! &amp;lt;br&amp;gt; Evaporate all excess Shellite with either a fan or just leave it alone until no scent of Shellite remains. &amp;lt;br&amp;gt; For your own curiosity you can let the Shellite you poured off evaporate slowly over a week or so and see if any DMT remained in the Shellite.&lt;br /&gt;
# Once the DMT is dry you can scrape it out and admire the end result of your hard work.&lt;br /&gt;
&lt;br /&gt;
Pictured is 5.9 grams of some damn clean spice &amp;lt;br&amp;gt; I attribute the ultra-high purity of the end result to the post-defat process used in this tech. &amp;lt;br&amp;gt; This yields a fairly low 0.3% (0.4&amp;amp;ndash;0.5% expected) however the tree used was very young (about 5 years old) which could be a major factor.&lt;br /&gt;
&lt;br /&gt;
== Reference ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Extraction Tek]]&lt;br /&gt;
[[Category:Acid/Base]]&lt;br /&gt;
[[Category:DMT]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Category:Extraction_Tek</id>
		<title>Category:Extraction Tek</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Category:Extraction_Tek"/>
				<updated>2013-11-29T20:35:19Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;An Extraction Tek is a manual to extract certain chemicals from a given source.&lt;br /&gt;
&lt;br /&gt;
To learn more about extractions in general and how they work, check the [http://wiki.dmt-nexus.me/FAQ#Where_to_start.3F FAQ], the [http://wiki.dmt-nexus.me/DMT_Extraction_Overview extraction overview], as well as read a few different teks, even if you don't plan on doing them, because many of them explain the processes and why each step is done.&lt;br /&gt;
&lt;br /&gt;
One does not need to be a chemist to perform an extraction. Don't worry about not understanding everything at first. Keep reading, inform yourself, take safety precautions, don't throw anything away before you're done with your extraction and don't consume anything you are not sure its clean.&lt;br /&gt;
&lt;br /&gt;
{{Main Page/Portal|[[Image:Information.png]]|'''[[:Category:Extraction_Tek|Extraction Teks]]'''|&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td&amp;gt;&lt;br /&gt;
==DMT==&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Lextek]]&lt;br /&gt;
* [[Marsofold's tek]]&lt;br /&gt;
* [[Shaggy's Jungle Tek]]&lt;br /&gt;
* [[The DMT Handbook]]&lt;br /&gt;
* [[Vovin's tek]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=39030 ACBR Tek By Thick-Light]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene and Fumaric Acid Approach]]&lt;br /&gt;
* [[Lazyman's tek]]&lt;br /&gt;
* [[Noman's tek]]&lt;br /&gt;
* [[STC - Dream Weaver's tek]]&lt;br /&gt;
&lt;br /&gt;
===STB-A/B hybrid===&lt;br /&gt;
&lt;br /&gt;
* [[BLAB_-_The_Big_Leisurely_AB|BLAB]]&lt;br /&gt;
* [[PanoraMIX European AB]]&lt;br /&gt;
* [[Nontoxic_limonene_tek|SyZyGyPSy's Nontoxic Limomene Tek]]&lt;br /&gt;
* [[Cyb's Hybrid ATB 'Salt' Tek]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Amor fati's Nontoxic Approach to Spice Extraction]]&lt;br /&gt;
* [[Q21Q21's Vinegar/Lime A/B Extraction Tek]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==MESCALINE==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's A/B Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[LucidLemonade's sunflower oil mescaline extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude extract===&lt;br /&gt;
&lt;br /&gt;
* [[House's cacti preparation tek]]&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[69ron's D-Limonene Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
==BUFOTENINE==&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene Bufotenine Extraction]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=10071 No smell bufo extraction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[Bufotenine IPA Extraction and Bufojam Changa Tek]]&lt;br /&gt;
&lt;br /&gt;
==HARMALAS==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Harmalas Extraction and Separation Guide]]&lt;br /&gt;
* [[EASY Harmaloid Freebase TEK]]&lt;br /&gt;
* [[Easy Caapi Vine Alkaloid Extraction Guide]]&lt;br /&gt;
* [[Enoons Cold Caapi Tek]]&lt;br /&gt;
* [[The Tao of Rue Extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude Manske (salt) Extract===&lt;br /&gt;
&lt;br /&gt;
* [[Harmine Crystals from Syrian Rue]]&lt;br /&gt;
&lt;br /&gt;
==LSA==&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX HBWR Extract]]&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's Advanced LSA Extraction]]&lt;br /&gt;
&lt;br /&gt;
==SALVIA==&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX salvia extact]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Tek]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Category:Extraction_Tek</id>
		<title>Category:Extraction Tek</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Category:Extraction_Tek"/>
				<updated>2013-11-29T20:15:04Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;An Extraction Tek is a manual to extract certain chemicals from a given source.&lt;br /&gt;
&lt;br /&gt;
To learn more about extractions in general and how they work, check the [http://wiki.dmt-nexus.me/FAQ#Where_to_start.3F FAQ], the [http://wiki.dmt-nexus.me/DMT_Extraction_Overview extraction overview], as well as read a few different teks, even if you don't plan on doing them, because many of them explain the processes and why each step is done.&lt;br /&gt;
&lt;br /&gt;
One does not need to be a chemist to perform an extraction. Don't worry about not understanding everything at first. Keep reading, inform yourself, take safety precautions, don't throw anything away before you're done with your extraction and don't consume anything you are not sure its clean.&lt;br /&gt;
&lt;br /&gt;
{{Main Page/Portal|[[Image:Information.png]]|'''[[:Category:Extraction_Tek|Extraction Teks]]'''|&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td&amp;gt;&lt;br /&gt;
==DMT==&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Lextek]]&lt;br /&gt;
* [[Marsofold's tek]]&lt;br /&gt;
* [[Shaggy's Jungle Tek]]&lt;br /&gt;
* [[The DMT Handbook]]&lt;br /&gt;
* [[Vovin's tek]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=39030 ACBR Tek By Thick-Light]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene and Fumaric Acid Approach]]&lt;br /&gt;
* [[Lazyman's tek]]&lt;br /&gt;
* [[Noman's tek]]&lt;br /&gt;
* [[STC - Dream Weaver's tek]]&lt;br /&gt;
&lt;br /&gt;
===STB-A/B hybrid===&lt;br /&gt;
&lt;br /&gt;
* [[BLAB_-_The_Big_Leisurely_AB|BLAB]]&lt;br /&gt;
* [[PanoraMIX European AB]]&lt;br /&gt;
* [[Nontoxic_limonene_tek|SyZyGyPSy's Nontoxic Limomene Tek]]&lt;br /&gt;
* [[Cyb's Hybrid ATB 'Salt' Tek]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Amor fati's Nontoxic Approach to Spice Extraction]]&lt;br /&gt;
* [[Q21Q21's Vinegar/Lime A/B Extraction Tek]]&lt;br /&gt;
&lt;br /&gt;
===Acid-Salt tek===&lt;br /&gt;
&lt;br /&gt;
* [[Spice Extraction-The FASA Approach]]&lt;br /&gt;
&lt;br /&gt;
==MESCALINE==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's A/B Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[LucidLemonade's sunflower oil mescaline extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude extract===&lt;br /&gt;
&lt;br /&gt;
* [[House's cacti preparation tek]]&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[69ron's D-Limonene Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
==BUFOTENINE==&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene Bufotenine Extraction]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=10071 No smell bufo extraction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[Bufotenine IPA Extraction and Bufojam Changa Tek]]&lt;br /&gt;
&lt;br /&gt;
==HARMALAS==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Harmalas Extraction and Separation Guide]]&lt;br /&gt;
* [[EASY Harmaloid Freebase TEK]]&lt;br /&gt;
* [[Easy Caapi Vine Alkaloid Extraction Guide]]&lt;br /&gt;
* [[Enoons Cold Caapi Tek]]&lt;br /&gt;
* [[The Tao of Rue Extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude Manske (salt) Extract===&lt;br /&gt;
&lt;br /&gt;
* [[Harmine Crystals from Syrian Rue]]&lt;br /&gt;
&lt;br /&gt;
==LSA==&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX HBWR Extract]]&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's Advanced LSA Extraction]]&lt;br /&gt;
&lt;br /&gt;
==SALVIA==&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX salvia extact]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Tek]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Category:Extraction_Tek</id>
		<title>Category:Extraction Tek</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Category:Extraction_Tek"/>
				<updated>2013-11-29T20:07:37Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;An Extraction Tek is a manual to extract certain chemicals from a given source.&lt;br /&gt;
&lt;br /&gt;
To learn more about extractions in general and how they work, check the [http://wiki.dmt-nexus.me/FAQ#Where_to_start.3F FAQ], the [http://wiki.dmt-nexus.me/DMT_Extraction_Overview extraction overview], as well as read a few different teks, even if you don't plan on doing them, because many of them explain the processes and why each step is done.&lt;br /&gt;
&lt;br /&gt;
One does not need to be a chemist to perform an extraction. Don't worry about not understanding everything at first. Keep reading, inform yourself, take safety precautions, don't throw anything away before you're done with your extraction and don't consume anything you are not sure its clean.&lt;br /&gt;
&lt;br /&gt;
{{Main Page/Portal|[[Image:Information.png]]|'''[[:Category:Extraction_Tek|Extraction Teks]]'''|&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td&amp;gt;&lt;br /&gt;
==DMT==&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Lextek]]&lt;br /&gt;
* [[Marsofold's tek]]&lt;br /&gt;
* [[Shaggy's Jungle Tek]]&lt;br /&gt;
* [[The DMT Handbook]]&lt;br /&gt;
* [[Vovin's tek]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=39030 ACBR Tek By Thick-Light]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene and Fumaric Acid Approach]]&lt;br /&gt;
* [[Lazyman's tek]]&lt;br /&gt;
* [[Noman's tek]]&lt;br /&gt;
* [[STC - Dream Weaver's tek]]&lt;br /&gt;
&lt;br /&gt;
===STB-A/B hybrid===&lt;br /&gt;
&lt;br /&gt;
* [[BLAB_-_The_Big_Leisurely_AB|BLAB]]&lt;br /&gt;
* [[PanoraMIX European AB]]&lt;br /&gt;
* [[Nontoxic_limonene_tek|SyZyGyPSy's Nontoxic Limomene Tek]]&lt;br /&gt;
* [[Cyb's Hybrid ATB 'Salt' Tek]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Amor fati's Nontoxic Approach to Spice Extraction]]&lt;br /&gt;
* [[Q21Q21's Vinegar/Lime A/B Extraction Tek]]&lt;br /&gt;
&lt;br /&gt;
===Salt tek===&lt;br /&gt;
&lt;br /&gt;
* [[Spice Extraction-The FASA Approach]]&lt;br /&gt;
&lt;br /&gt;
==MESCALINE==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's A/B Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
===STB===&lt;br /&gt;
&lt;br /&gt;
* [[LucidLemonade's sunflower oil mescaline extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude extract===&lt;br /&gt;
&lt;br /&gt;
* [[House's cacti preparation tek]]&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[69ron's D-Limonene Mescaline Extraction]]&lt;br /&gt;
&lt;br /&gt;
==BUFOTENINE==&lt;br /&gt;
&lt;br /&gt;
===Dry tek===&lt;br /&gt;
&lt;br /&gt;
* [[Jorkest's D-Limonene Bufotenine Extraction]]&lt;br /&gt;
* [[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=10071 No smell bufo extraction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[Bufotenine IPA Extraction and Bufojam Changa Tek]]&lt;br /&gt;
&lt;br /&gt;
==HARMALAS==&lt;br /&gt;
&lt;br /&gt;
===A/B===&lt;br /&gt;
&lt;br /&gt;
* [[Harmalas Extraction and Separation Guide]]&lt;br /&gt;
* [[EASY Harmaloid Freebase TEK]]&lt;br /&gt;
* [[Easy Caapi Vine Alkaloid Extraction Guide]]&lt;br /&gt;
* [[Enoons Cold Caapi Tek]]&lt;br /&gt;
* [[The Tao of Rue Extraction]]&lt;br /&gt;
&lt;br /&gt;
===Crude Manske (salt) Extract===&lt;br /&gt;
&lt;br /&gt;
* [[Harmine Crystals from Syrian Rue]]&lt;br /&gt;
&lt;br /&gt;
==LSA==&lt;br /&gt;
&lt;br /&gt;
===IPA extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX HBWR Extract]]&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[Kash's Advanced LSA Extraction]]&lt;br /&gt;
&lt;br /&gt;
==SALVIA==&lt;br /&gt;
&lt;br /&gt;
===Acetone extract===&lt;br /&gt;
&lt;br /&gt;
* [[PanoraMIX salvia extact]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Tek]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Psychedelic_Compounds_Chemical_and_Physical_Properties</id>
		<title>Psychedelic Compounds Chemical and Physical Properties</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Psychedelic_Compounds_Chemical_and_Physical_Properties"/>
				<updated>2013-11-28T22:27:07Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* DMT N-Oxide */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;For more detailed information on each compound, please visit their individual wikis as linked in the [[:Category:Alkaloids|Alkaloids]] section&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Psychedelic Compounds Chemical and Physical Properties ==&lt;br /&gt;
&lt;br /&gt;
=== DMT ===&lt;br /&gt;
N,N-Dimethyltryptamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase DMT ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:dmtfreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Appearance: White/Transparent crystals&lt;br /&gt;
* CAS Registry Number:  61-50-7&lt;br /&gt;
* Composition: C12H16N2&lt;br /&gt;
* Molecular Weight: 188.26884 g/mol&lt;br /&gt;
* Melting point: 44-68°C (Conflicting reports in literature, as mentioned in [http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* Boiling point: Theoretically 360-380°C&lt;br /&gt;
* XLogP: 2.0&lt;br /&gt;
* XLogP3: 2.5 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=6089&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
* pKa: 8.68 ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Stability/Degradation: Oxidation to DMT N-Oxide (yellow oil) in extended presence of oxygen (specialy in evaporation of dmt-containing solvents with heat and/or fan or generally in prolonged exposure to open air). N-oxide may be reverted back to the parent compound by reduction, as described [http://www.anoniem.org/?http://wiki.dmt-nexus.me/DMT_N-Oxide_to_Freebase_DMT in the N-Oxide to Freebase Wiki].&lt;br /&gt;
* Solubility: &lt;br /&gt;
Very Soluble in Xylene, Toluene, Limonene, acetone, Isopropyl Alcohol (IPA), methanol, ethanol, Dichloromethane (DCM), chloroform, ether, Butanone (also known as methyl ethyl ketone (MEK)) and butanol.&lt;br /&gt;
&lt;br /&gt;
Soluble in naphtha, hexane, heptane but almost insoluble in these solvents at freezing temperatures&lt;br /&gt;
&lt;br /&gt;
Almost insoluble in water.&lt;br /&gt;
&lt;br /&gt;
==== DMT N-Oxide ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:dmtnoxide.jpg]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Appearance: Basic oil (Weak base. Weaker than DMT, NMT or tryptamine.) Fish et al. 1956.  Hygroscopic solid Banerjee &amp;amp; Ghosal 1969&lt;br /&gt;
* XLogP3: 2&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in Xylene, Toluene, Limonene (?)&lt;br /&gt;
Soluble in chloroform Bane1 and Ghosal 1969&lt;br /&gt;
Soluble in water. Fish et al. 1955 and Ghosal et al. 1970b and Banerjee &amp;amp; Ghosal 1969&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Insoluble in petroleum (naphtha) but appreciably soluble in petroleum which contains fats. Ghosal &amp;amp; Banerjee 1969&lt;br /&gt;
&lt;br /&gt;
* Interconversion: It has been claimed that DMT N-Oxide can be reconverted back to [[DMT]] by redissolving in dilute acetic acid solution, adding excess zinc dust, mixing for a couple of hours, filtering to remove zinc, adding base and pulling with organic solvent as in a normal extraction.   [[DMT]] can be oxidized by using hydrogen peroxide ([https://www.dmt-nexus.me/forum/resource.ashx?a=7966 Fish et al 1955])&lt;br /&gt;
&lt;br /&gt;
==== DMT Fumarate ====&lt;br /&gt;
&lt;br /&gt;
* Molecular Weight: 492.608 g/mol&lt;br /&gt;
* Solubility:&lt;br /&gt;
Very soluble in water&lt;br /&gt;
&lt;br /&gt;
Soluble in methanol (~10mg/ml) &lt;br /&gt;
&lt;br /&gt;
Soluble in boiling IPA, Practically insoluble in room temp IPA (~1mg/ml), Insoluble in freeze-cold IPA.&lt;br /&gt;
&lt;br /&gt;
Slightly soluble in ethanol (~5mg/ml)&lt;br /&gt;
&lt;br /&gt;
Insoluble in cold acetone&lt;br /&gt;
&lt;br /&gt;
Insoluble in FASI (Fumaric Acid Saturated IPA)&lt;br /&gt;
&lt;br /&gt;
Insoluble in FASA (Fumaric Acid Saturated Acetone)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===NMT ===&lt;br /&gt;
N-Methyltryptamine, monomethyltryptamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase NMT ====&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:Nmt.jpg]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Appearance: Oil, difficult crystallization, eventually forms crystalline stellar aggregates, darkens with exposure to air ([https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544&amp;amp;p=2 Source 1], [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Source 2])&lt;br /&gt;
* Composition: C11H14N2&lt;br /&gt;
* Molecular Weight: 174.24226 g/mol&lt;br /&gt;
* Melting point: 87-89C (Sigma Aldrich)&lt;br /&gt;
* Boiling point: 336.181 °C at 760 mmHg ([http://www.chemspider.com/Chemical-Structure.11523514.html Chemspider])&lt;br /&gt;
* XLogP3: 2.1 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=6088 PubChem])&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Stability/Degradation: Darkens over time, but does not seem to form oxides ([https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544&amp;amp;p=2 Source] )&lt;br /&gt;
* Solubility: &lt;br /&gt;
Soluble in methanol, warm ethanol, dichloromethane &amp;amp; choloroform. Soluble to some extent in naphtha (not nearly as much as DMT). It seemed only partially soluble in warm acetic acid. It is likely soluble in xylene. ([https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544&amp;amp;p=2 Source] )&lt;br /&gt;
* Pharmacology and activity: &lt;br /&gt;
-Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
- 1/3 to 1/4 potency of DMT [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
=== 5-MeO-DMT ===&lt;br /&gt;
5-methoxy-N,N-dimethyl-tryptamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase 5-MeO-DMT ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:5meodmtfreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Appearance: Off-white crystals (Sigma Aldrich)&lt;br /&gt;
* Composition: C13H18N20&lt;br /&gt;
* Molecular Weight: 218.298 g/mol&lt;br /&gt;
* Melting Point: 66-67°C, 67-68°C, 69-70°C (Trout's notes and [http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* Boiling Point4 : 208-210°C @ 4mm (Hoshino &amp;amp; Shimodaira 1936)&lt;br /&gt;
* XLogP: 1.9&lt;br /&gt;
* XLogP3: 1.5 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=1832&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
* pKa: 9.3 (Ghosal &amp;amp; Mukherjee 1964)&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Stability: Stable under normal temperatures and pressures. Incompatible with strong oxidizing agents, strong acids ([http://ch3v1.chemexper.com/cheminfo/servlet/org.dbcreator.MainServlet?sort=&amp;amp;query=msds._msdsID%3D11173&amp;amp;target=msds&amp;amp;action=PowerSearch&amp;amp;from=0&amp;amp;format=ccd&amp;amp;searchValue=j%60qQ%40%40IVAdbfRfTJTYrRj%40Bfjb%40%40%40&amp;amp;history=off&amp;amp;realQuery=structure._structureID%3D4638142&amp;amp;onclick=1&amp;amp;selectionInfo=&amp;amp;searchTemplate=uniqueMol.structureString%3D%3F+elsor+uniqueMol.structureID%3D%3F&amp;amp;options=brandqtyoffer Source])&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in: Chloroform, ether, DCM, acetone, methanol, ethanol (Trout's notes on simple tryptamines). Soluble in (at least) 20mg/ml 96% ethanol ([https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=176401#post176401 Source]). &lt;br /&gt;
&lt;br /&gt;
Hexane/Naphtha/Pet ether are commonly used to crystallize it (Ott 1993, Espamer et al 1967, Morimoto &amp;amp; Matsumoto 1966, etc) , so it is probably moderately soluble in these solvents.&lt;br /&gt;
&lt;br /&gt;
Practically Insoluble in water ([http://ch3v1.chemexper.com/cheminfo/servlet/org.dbcreator.MainServlet?sort=&amp;amp;query=msds._msdsID%3D11173&amp;amp;target=msds&amp;amp;action=PowerSearch&amp;amp;from=0&amp;amp;format=ccd&amp;amp;searchValue=j%60qQ%40%40IVAdbfRfTJTYrRj%40Bfjb%40%40%40&amp;amp;history=off&amp;amp;realQuery=structure._structureID%3D4638142&amp;amp;onclick=1&amp;amp;selectionInfo=&amp;amp;searchTemplate=uniqueMol.structureString%3D%3F+elsor+uniqueMol.structureID%3D%3F&amp;amp;options=brandqtyoffer Source])&lt;br /&gt;
&lt;br /&gt;
==== 5-MeO-DMT Hydrochloride====&lt;br /&gt;
* Melting Point: 145-146°C ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Bufotenine ===&lt;br /&gt;
5-HO-DMT - 5-hydroxy-N,N-dimethyl-tryptamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Bufotenine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:bufoteninefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number:  487-93-4&lt;br /&gt;
* Composition: C12H16N2O&lt;br /&gt;
* Molecular Weight: 204.268 g/mol&lt;br /&gt;
* Melting point:146–147 °C (295–297 °F)&lt;br /&gt;
* Boiling point: 320 °C (608 °F)&lt;br /&gt;
* XLogP: 1.6&lt;br /&gt;
* XLogP3: 1.2 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
* pKa: 9.67&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility:&lt;br /&gt;
Acetone @ 20 C: soluble (5 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
Chloroform @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Dichloromethane @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Dimethyl sulfoxide (DMSO) @ 20 C: soluble (6 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
D-Limonene (Orange Oil) @ 20 C: insoluble&lt;br /&gt;
&lt;br /&gt;
D-Limonene (Orange Oil) @ 176 C: soluble (more than 1.7 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
Dilute Acids and Alkalis: Soluble ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
&lt;br /&gt;
Ethanol @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Ether @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Ethyl acetate @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Heptane @ 20 C: insoluble&lt;br /&gt;
&lt;br /&gt;
Heptane with 40% MEK @ 20 C: soluble (0.53 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
Heptane with 50% MEK @ 20 C: soluble (1.22 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
IPA @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
MEK @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Methanol @ 20 C: soluble&lt;br /&gt;
&lt;br /&gt;
Naphtha @ 20 C: insoluble&lt;br /&gt;
&lt;br /&gt;
Water @ 20 C: nearly insoluble in pure water (no acid or alkali added)&lt;br /&gt;
&lt;br /&gt;
Xylene @ 20 C: nearly insoluble (less than 0.03 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
Xylene @ 144 C: soluble (1.5 g/100 ml)&lt;br /&gt;
&lt;br /&gt;
==== Bufotenine Fumarate ====&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in water&lt;br /&gt;
&lt;br /&gt;
Insoluble in FASA (Fumaric Acid Saturated Acetone)&lt;br /&gt;
&lt;br /&gt;
=== Psilocin ===&lt;br /&gt;
4-HO-DMT - 4-Hydroxy-N,N-dimethyl-tryptamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Psilocin ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:psilocinfreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number:  520-53-6&lt;br /&gt;
* Composition: C12H16N2O&lt;br /&gt;
* Molecular Weight: 204.27 g/mol&lt;br /&gt;
* Melting Point: 103-104°C ([http://isomerdesign.com/PiHKAL/read.php?domain=tk&amp;amp;id=18 TIHKAL]) , 173-176°C (Merck Index)&lt;br /&gt;
* XLogP3: 2.1 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Stability/Degradation: Unstable in solution, especially alkaline solution (Merck Index).&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in 70% ethanol. Poorly soluble in dry ethanol, and poorly soluble in ethanol less than 60%. Very slightly soluble in water (sources: [http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;br /&gt;
&lt;br /&gt;
=== Psilocybin ===&lt;br /&gt;
4-PO-DMT - O-phosphoryl-4-hydroxy-N,N-dimethyltryptamine&lt;br /&gt;
&lt;br /&gt;
==== Psilocybin (Psilocin Phosphate Ester) ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:psilocybin.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number:  520-52-5&lt;br /&gt;
* Composition: C12H17N2O4P&lt;br /&gt;
* Molecular Weight: 284.248141 g/mol&lt;br /&gt;
* Melting Point: 220-228° from boiling water; 185-195° from boiling methanol ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
Free base:&lt;br /&gt;
Stable compound. Colorless crystals. Hofmann 1971&lt;br /&gt;
pH 5.2 (in 50% EtOH) Merck 9th&lt;br /&gt;
More stable than psilocin. Shulgin &amp;amp; Shulgin !997&lt;br /&gt;
mp 175-180° Repke &amp;amp; leslie 1977&lt;br /&gt;
mp 185-195° (from boiling methanol) Ott 1996&lt;br /&gt;
mp 185-195° (from methanol) Picker &amp;amp; Rickards 1970&lt;br /&gt;
(Also in Perkal 1981)&lt;br /&gt;
rnp 185-195° (dec.) (white crystals) Clarke 's 1986&lt;br /&gt;
mp 190° Mantle &amp;amp; Waight 1969&lt;br /&gt;
&lt;br /&gt;
* XLogP3: -1.6 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=10624&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Stability/Degradation: Dephosphorylated into Psilocin under acidic conditions. Also when ingested, by phosphatases enzymes.&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in water. Soluble in 20 parts boiling water (= 0.79g/ml in boiling water), 120 parts boiling methanol (= 0.0932g/ml in boiling methanol); very soluble in 70% methanol saturated with KNO3, soluble in dry methanol, difficultly soluble in ethanol, increasingly less soluble in methanol less than 80%. Practically insoluble in chloroform, benzene (sources: [http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;br /&gt;
&lt;br /&gt;
=== Mescaline ===&lt;br /&gt;
3,4,5-trimethoxyphenethylamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Mescaline ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:mescalinefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number:  54-04-6&lt;br /&gt;
* Composition: C11H17NO3&lt;br /&gt;
* Melting point: 35-36°C (Kindler and Peschke, 103.  [http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Boiling point: 180°C (12 mmHg)&lt;br /&gt;
* XLogP: 0.6 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
* XLogP3: 0.7 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=4076&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
* pKa: 9.56&lt;br /&gt;
* Appearance: long needle shaped white crystals&lt;br /&gt;
* Molecular weight: 211.26&lt;br /&gt;
Notes: forms mescaline carbonate on prolonged exposure to air&lt;br /&gt;
* Average dose: 300 to 600 milligrams with a duration of 5 to 12 hours.&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility&lt;br /&gt;
Soluble in: alcohol, chloroform, benzene, xylene, toluene, acetone, dichloromethane, highly soluble in isopropyl alcohol, soluble in d-limonene&lt;br /&gt;
&lt;br /&gt;
Moderately soluble in: water&lt;br /&gt;
&lt;br /&gt;
Insoluble in: practically insoluble in ether or petroleum ether&lt;br /&gt;
* LD50: i.p. rats 370 mg/kg&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Citrate ====&lt;br /&gt;
* Solubility&lt;br /&gt;
Soluble in water&lt;br /&gt;
&lt;br /&gt;
Insoluble in: xylene, acetone &amp;lt;nowiki&amp;gt;*&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;nowiki&amp;gt;*&amp;lt;/nowiki&amp;gt; Possible unreliable web source.&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Hydrochloride ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:mescalinehcl.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Molecular weight: 247.72 (Sigma Aldrich)&lt;br /&gt;
* Empirical Formula (Hill Notation): C11H17NO3 • HCl (Sigma Aldrich)&lt;br /&gt;
* CAS Number: 832-92-8&lt;br /&gt;
* Appearance: colorless crystals, needles&lt;br /&gt;
* Melting point: 184°C ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Solubility:&lt;br /&gt;
Moderately soluble in: water, alcohol ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index]), methanol (at least 1.0 mg/ml, source Sigma Aldrich solution)&lt;br /&gt;
(Merck Index)&lt;br /&gt;
Insoluble in: practically insoluble in toluene and acetone, insoluble in isopropyl alcohol, diethyl ether, and d-limonene&lt;br /&gt;
* LD50: i.p. rats 132 mg/kg&lt;br /&gt;
* Storage temperature: 2-8°C (Sigma Aldrich)&lt;br /&gt;
* Isolation: when mescaline hydrochloride is extracted from San Pedro, Achuma, or Peruvian torch, it can be isolated from the other alkaloids by washing it in IPA or acetone (use 10 ml per gram of alkaloids, and wash 2-3 times).  The non-mescaline alkaloids dissolve in the IPA or acetone (* NOTE: previous sentence is speculation, not yet substantiated by tests as far as we know), while the mescaline hydrochloride does not. Note that for the cleanest results use about 2 washes of acetone, and then 2 washes with IPA.&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Picrate ====&lt;br /&gt;
* Melting point: mp 222°C.&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Sulfate Dihydrate====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:mescalinesulfate.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: (C11H17NO3)2 • H2SO4 • 2H2O&lt;br /&gt;
* Appearance: prisms&lt;br /&gt;
* Melting point: 183–186 °C (361–367 °F)&lt;br /&gt;
* Molecular Weight: 309.33606&lt;br /&gt;
* Soluble in: hot water, methanol&lt;br /&gt;
* Almost insoluble in: near freezing water, alcohol, acetone &amp;lt;nowiki&amp;gt;*&amp;lt;/nowiki&amp;gt;  [VERIFIED]&lt;br /&gt;
&amp;lt;nowiki&amp;gt;*&amp;lt;/nowiki&amp;gt; Possible unreliable web source.&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Fumarate ====&lt;br /&gt;
* Composition: unknown (it may be a one to one salt or may not be)&lt;br /&gt;
* Appearance: White powder&lt;br /&gt;
* Melting point: unknown&lt;br /&gt;
* Solubility&lt;br /&gt;
Soluble in: water&lt;br /&gt;
&lt;br /&gt;
Insoluble in: Limonene, Anydrous IPA, Acetone, MEK (most likely insoluble in all non-polars like xylene and toluene) [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=18705 Source]&lt;br /&gt;
&lt;br /&gt;
==== Mescaline Acetate ====&lt;br /&gt;
* Composition: unknown&lt;br /&gt;
* Appearance: white free flowing powder with a slight waxy texture &amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
* Melting point: unknown&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in: water&amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt;, isopropyl alcohol&amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt;, acetone&amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt;, DMSO&amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt; (more than 5 grams/100 ml), boiling MEK***&lt;br /&gt;
&lt;br /&gt;
Insoluble in: xylene, d-limonene, cold MEK (Methyl Ethyl Ketone) &amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;nowiki&amp;gt;***&amp;lt;/nowiki&amp;gt; This information was validated by SWIM and is reliable.&lt;br /&gt;
* Isolation: when mescaline acetate is extracted from San Pedro, Achuma, or Peruvian torch, it can be isolated from the other alkaloids by washing it in cold MEK (use 10 ml per gram of alkaloids, and wash 2-3 times). The non-mescaline alkaloids dissolve in the MEK, while the mescaline acetate does not. Mescaline acetate can be recrystallized in MEK by boiling the MEK and then freezing it overnight.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Ibogaine ===&lt;br /&gt;
12-methoxyibogamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Ibogaine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:ibogainefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number:  83-74-9&lt;br /&gt;
* Composition: C20H26N2O&lt;br /&gt;
* Molecular Weight: 310.43324 g/mol&lt;br /&gt;
* Melting Point: 152-153 °C ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* XLogP3: 3.9 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
* pKa: 8.1 in 80% methylcellosolve ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility: Soluble in limonene ([http://www.anoniem.org/?https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=10651 Non-Toxic Iboga Extraction]) soluble in acetone (merck)&lt;br /&gt;
&lt;br /&gt;
==== Ibogaine Hydrochloride ====&lt;br /&gt;
* Melting Point: 299-300 °C ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* Solubility: Soluble in water, methanol (Sigma Aldrich), slightly soluble in acetone (merck)&lt;br /&gt;
&lt;br /&gt;
=== Voacangine ===&lt;br /&gt;
12-methoxyibogamine-18-carboxylic acid methyl ester&lt;br /&gt;
&lt;br /&gt;
==== Voacangine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:voacangine.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C22H28N2O3&lt;br /&gt;
* Molecular Weight: 368.46932 g/mole&lt;br /&gt;
* Melting Point: 136–137 °C ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* pKa: 7.4 (40% aq methanol); 5.73 (33% DMF)  ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* XLogP3-AA: 3.5 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
&lt;br /&gt;
=== LSA (ergine) ===&lt;br /&gt;
Lysergamide &lt;br /&gt;
&lt;br /&gt;
==== Freebase LSA ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:lsafreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
CAS Registry Number:  478-94-4&lt;br /&gt;
* Composition: C16H17N3O&lt;br /&gt;
* Molecular Weight: 267.32568 g/mol&lt;br /&gt;
* XLogP3: 1.6 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=442072&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
&lt;br /&gt;
=== Muscimol ===&lt;br /&gt;
Pantherine, Agarine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Muscimol ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:muscimolfreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Appearance: White powder (Sigma Aldrich)&lt;br /&gt;
* CAS Registry Number:  2763-96-4&lt;br /&gt;
* Composition: C4H6N2O2&lt;br /&gt;
* Molecular Weight: 114.10264 g/mol&lt;br /&gt;
* Melting Point: 175°C (Merck Index)&lt;br /&gt;
* Boiling Point: 70°C (Wolfram Alpha)&lt;br /&gt;
* XLogP3-AA: -1.4 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=4266&amp;amp;loc=ec_rcs PubChem])&lt;br /&gt;
* pKa: 4.8 (Indiana University])&lt;br /&gt;
* Solubility: Very soluble in water and methanol, slightly soluble in ethanol, DMSO and DMF. ~10mg/ml in phosphate buffered saline @ pH 7.2 ([http://www.caymanchem.com/pdfs/13667.pdf Caymanchem.com])&lt;br /&gt;
&lt;br /&gt;
=== Salvinorin A ===&lt;br /&gt;
Note: Technically NOT an alkaloid, as it contains no nitrogen. It is a trans-neoclerodane diterpene.&lt;br /&gt;
&lt;br /&gt;
==== Salvinorin A ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:salvinorina.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C23H28O8&lt;br /&gt;
* Molecular Weight: 432.46362 g/mol&lt;br /&gt;
* Melting Point:242-244 – 238-240 °C (Wikipedia)&lt;br /&gt;
* Boiling Pont: 760.2 °C (1400 °F) (Wikipedia)&lt;br /&gt;
* XLogP3-AA: 2.5 ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Elemicin ===&lt;br /&gt;
1,2,3-trimethoxy-5-allylbenzene&lt;br /&gt;
&lt;br /&gt;
Note: Technically NOT an alkaloid, as it contains no nitrogen.&lt;br /&gt;
&lt;br /&gt;
==== Elemicin ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:elemicin.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
* CAS Number:  487-11-6&lt;br /&gt;
* Molecular Formula: C12H16O3&lt;br /&gt;
* Molecular Weight: 208.25364 g/mol&lt;br /&gt;
* Boiling Point: 152-156 °C @ 17 mmHg, 144-147 °C @ 10 mmHg ([http://www.thegoodscentscompany.com/data/rw1021681.html Source]), 146-147 °C ([http://www.chemyq.com/En/xz/xz3/20815lmxvj.htm Source 1] [http://www.chunyuan.com.cn/zhanshishow.asp?id=94 Source 2]), 279.8 °C @ 760 mmHg ([http://www.chemspider.com/Chemical-Structure.9830.html ChemSpider])&lt;br /&gt;
* XlogP3: 2.5  ([http://pubchem.ncbi.nlm.nih.gov/ PubChem])&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in alcohol, Insoluble in water ([http://www.thegoodscentscompany.com/data/rw1021681.html Source])&lt;br /&gt;
&lt;br /&gt;
=== Harmine ===&lt;br /&gt;
7-methoxy-β-carboline&lt;br /&gt;
&lt;br /&gt;
==== Freebase Harmine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:harminefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C13H12N2O&lt;br /&gt;
* Molecular Weight: 212.25 (Sigma Aldrich)&lt;br /&gt;
* Melting point: 262-264 °C (Sigma Aldrich)&lt;br /&gt;
* Boiling point: 421.4°Cat760mmHg ([http://www.lookchem.com/cas-442/442-51-3.html Lookchem])&lt;br /&gt;
* XLogP: 2.5&lt;br /&gt;
* XLogP3: 3.6&lt;br /&gt;
* pKa: 7.7&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility:&lt;br /&gt;
Insoluble in basic water, poorly soluble in distilled water. Reasonably soluble in acetone (at 25°C, acetone can dissolve 4mg/ml mixed harmalas as [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=200200#post200200 this test shows])&lt;br /&gt;
* Isolation: To separate from harmaline, using pKa properties, raise pH of solution containing both alkaloids to pH 8.75 to precipitate 92% of harmine and only 8% Harmaline. Filter to retrieve precipitated alkaloids, and raise the pH further to retrieve the bulk of harmaline. Check the [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=5725 freebase percentage calculator thread] and the [http://wiki.dmt-nexus.me/Harmalas_Extraction_and_Separation_Guide Harmala Extraction Guide] for more info.&lt;br /&gt;
&lt;br /&gt;
==== Harmine Hydrochloride ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:harminehcl.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Melting Point: 321 °C&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in water&lt;br /&gt;
&lt;br /&gt;
Insoluble in salt-saturated water&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Harmaline ===&lt;br /&gt;
3,4-dihydro-7-methoxy-1-methyl-β-carboline&lt;br /&gt;
&lt;br /&gt;
==== Freebase Harmaline ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:harmaline.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C13H14N2O&lt;br /&gt;
* Melting point: 232-234 °C (Sigma Aldrich)&lt;br /&gt;
* Boiling point: 120-140 °C at 0.001 mm/Hg ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* XLogP: 0.8&lt;br /&gt;
* XLogP3: 1.2&lt;br /&gt;
* pKa: 9.8&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility:&lt;br /&gt;
Slightly soluble in basic water, poorly soluble in distilled water. Reasonably soluble in acetone (at 25°C, acetone can dissolve 4mg/ml mixed harmalas as [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=200200#post200200 this test shows])&lt;br /&gt;
* Isolation: To separate from harmine, using pKa properties, raise pH of solution containing both alkaloids to pH 8.75 to precipitate 92% of harmine and only 8% Harmaline. Filter to retrieve precipitated alkaloids, and raise the pH further to retrieve the bulk of harmaline. Check the [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=5725 freebase percentage calculator thread] and the [http://wiki.dmt-nexus.me/Harmalas_Extraction_and_Separation_Guide Harmala Extraction Guide] for more info.&lt;br /&gt;
&lt;br /&gt;
==== Harmaline Hydrochloride ====&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in water&lt;br /&gt;
&lt;br /&gt;
Insoluble in salt-saturated water&lt;br /&gt;
&lt;br /&gt;
=== THH ===&lt;br /&gt;
Tetrahydroharmine - 7-methoxy-1-methyl-1,2,3,4-tetrahydro-β-carboline&lt;br /&gt;
&lt;br /&gt;
==== Freebase THH ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:thhfreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C13H16N2O&lt;br /&gt;
* Molecular Weight: 216.27894 g/mol&lt;br /&gt;
* Melting Point: 187-190 °C ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* XlogP: 1.9&lt;br /&gt;
* XLogP3: 1.9&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* Solubility:&lt;br /&gt;
Soluble in chloroform, ethanol &amp;amp; methanol. (Ott 1996.)&lt;br /&gt;
&lt;br /&gt;
Soluble in ethyl acetate. (Siddiqui et al. 1983)&lt;br /&gt;
&lt;br /&gt;
Poorly soluble in distilled water &lt;br /&gt;
&lt;br /&gt;
==== THH Hydrochloride ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:thhhcl.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C13H17ClN2O&lt;br /&gt;
* Molecular Weight: 252.73988 g/mol&lt;br /&gt;
* Melting Point: 232–234 °C ([http://isomerdesign.com/PiHKAL/browse.php?domain=tk TIHKAL])&lt;br /&gt;
* Boiling point: 399.2 °C at 760 mmHg ([http://www.lookchem.com/TETRAHYDROHARMINE Lookchem])&lt;br /&gt;
* Mol File: 40959-16-8.mol &lt;br /&gt;
* Flash Point: 195.2 °C &lt;br /&gt;
* Enthalpy of Vaporization: 64.99 kJ/mol &lt;br /&gt;
* Vapour Pressure: 1.4E-06 mmHg at 25°C &lt;br /&gt;
* H-Bond Donor: 3&lt;br /&gt;
* H-Bond Acceptor: 2&lt;br /&gt;
* Rotatable Bond Count: 1 &lt;br /&gt;
* Topological Polar Surface Area: 37.1 &lt;br /&gt;
* Heavy Atom Count: 17 &lt;br /&gt;
* Complexity: 258&lt;br /&gt;
&lt;br /&gt;
== Relevant NOT psychedelic compounds ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Gramine ===&lt;br /&gt;
N,N-Dimethyl-1H-indole-3-methanamine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Gramine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:graminefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* Composition: C11H14N2&lt;br /&gt;
* Molecular Weight: 174.24226 g/mol&lt;br /&gt;
* Melting point: 138-139°C (Merck)&lt;br /&gt;
* Boiling point:&lt;br /&gt;
* XLogP3: 1.8&lt;br /&gt;
* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;br /&gt;
* pKa: 8.52&lt;br /&gt;
* Solubility:&lt;br /&gt;
Sol in alcohol, ether, chloroform; slightly sol in cold acetone. Practically insol in petr ether, water. (Merck Index)&lt;br /&gt;
&lt;br /&gt;
=== Hordenine ===&lt;br /&gt;
N,N-dimethyltyramine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Hordenine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:hordeninefreebase.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number: 539-15-1&lt;br /&gt;
* Composition: C10H15NO&lt;br /&gt;
* Molecular Weight: 165.23 g/mol&lt;br /&gt;
* Melting point: 117-118° ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Boiling point: 173° @ 11mmHg ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* XlogP3: 2.1 (PubChe[[File:m)&lt;br /&gt;
* Solubility:&lt;br /&gt;
Very sol in alcohol, chloroform, ether. 7 grams dissolve in 1000 ml water. Sparingly sol in benzene, toluene, xylene. Practically insol in petr ether. ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
&lt;br /&gt;
==== Hordenine Hydrochloride ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:hordeninehcl.png]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
* CAS Registry Number: 6027-23-2&lt;br /&gt;
* Composition: C10H15NO.HCl&lt;br /&gt;
* Molecular Weight: 201.70 g/mol&lt;br /&gt;
* Melting point: 177° ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
* Solubility:&lt;br /&gt;
Very sol in water. ([http://wiki.dmt-nexus.me/w/images/8/81/MERCK.pdf Merck Index])&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Vasicine ===&lt;br /&gt;
(3R)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol;Peganine&lt;br /&gt;
&lt;br /&gt;
==== Freebase Vasicine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:vasicine.jpg]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
* Composition: 	C11H12N2O&lt;br /&gt;
* Molecular Weight: 188.22578 g/mol&lt;br /&gt;
* Melting point: 209-211° C (Decomposes) ([http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm source])&lt;br /&gt;
* XLogP3: 0.4 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=442935&amp;amp;loc=ec_rcs pubchem])&lt;br /&gt;
* Pharmacology: Uterotonic, abortifacient, bronchodilatory activity, expectorant, respiratory stimulant activity, moderate hypotensive activity (sources: [http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm 1], [http://indianmedicine.eldoc.ub.rug.nl/root/A/2091/ 2]&lt;br /&gt;
* Solubility: Soluble in NaCl-saturated water (harmalas precipitate as HCl salts in NaCl-saturated water, hence vasicine can be separated from harmalas in peganum harmala. Check [http://wiki.dmt-nexus.me/Harmalas_Extraction_and_Separation_Guide harmala extraction guide for more info])&lt;br /&gt;
&lt;br /&gt;
=== Vasicinone ===&lt;br /&gt;
(R)-2,3-dihydro-3-hydroxypyrrolo(2,1-b)quinazolin-9(1H)-one&lt;br /&gt;
&lt;br /&gt;
==== Freebase Vasicinone ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:vasicinone.jpg]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
* Appearance: White powder&lt;br /&gt;
* Composition: 	C11H10N2O2&lt;br /&gt;
* Molecular Weight: 202.2093 g/mol&lt;br /&gt;
* Melting point: 203°-204° C  ([http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm source])&lt;br /&gt;
* XLogP3: 0.4 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=442935&amp;amp;loc=ec_rcs pubchem])&lt;br /&gt;
* Pharmacology: Uterotonic, abortifacient, bronchodilatory activity, expectorant, respiratory stimulant activity, moderate hypotensive activity (sources: [http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm 1], [http://indianmedicine.eldoc.ub.rug.nl/root/A/2091/ 2]&lt;br /&gt;
* Solubility: Water: 1600 mg/l. Soluble in NaCl-saturated water (harmalas precipitate as HCl salts in NaCl-saturated water, hence vasicinone can be separated from harmalas in peganum harmala. Check [http://wiki.dmt-nexus.me/Harmalas_Extraction_and_Separation_Guide harmala extraction guide for more info]&lt;br /&gt;
&lt;br /&gt;
=== Deoxyvasicine ===&lt;br /&gt;
1,2,3,9-Tetrahydropyrrolo(2,1-b)quinazoline; Deoxypeganin;&lt;br /&gt;
&lt;br /&gt;
==== Freebase Deoxyvasicine ====&lt;br /&gt;
&amp;lt;table&amp;gt;&amp;lt;tr&amp;gt;&amp;lt;td&amp;gt;[[Image:deoxyvasicine.jpg]]&amp;lt;/td&amp;gt;&amp;lt;td&amp;gt;&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
* Appearance: White to yellow powder&lt;br /&gt;
* Composition: C11H12N2&lt;br /&gt;
* Molecular Weight: 172.22638 g/mol&lt;br /&gt;
* Melting point: 86-87° C  ([http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm source])&lt;br /&gt;
* XLogP3: 0.4&lt;br /&gt;
* Pharmacology: Uterotonic, abortifacient, bronchodilatory activity, expectorant, respiratory stimulant activity, moderate hypotensive activity (sources: [http://www.chemicalland21.com/specialtychem/nd/VASICINE.htm 1], [http://indianmedicine.eldoc.ub.rug.nl/root/A/2091/ 2]&lt;br /&gt;
* Solubility: Water: 1600 mg/l. Soluble in NaCl-saturated water (harmalas precipitate as HCl salts in NaCl-saturated water, hence vasicine can be separated from harmalas in peganum harmala. Check [http://wiki.dmt-nexus.me/Harmalas_Extraction_and_Separation_Guide harmala extraction guide for more info])&lt;br /&gt;
&lt;br /&gt;
== Solvents and Alkaloids XlogP and XlogP3 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Alkaloid XlogP list'''&lt;br /&gt;
&lt;br /&gt;
* 0.1 - 6-methoxy-2-methyl-beta-Carboline&lt;br /&gt;
* 0.7 - Beta-carboline, 6-methoxy-1,2-dimethyl-1,2-Dimethyl-2H-beta-carbolin-6-yl methyl ether&lt;br /&gt;
* 0.7 - Mescaline&lt;br /&gt;
* 0.8 - Harmaline&lt;br /&gt;
* 1.0 - 5-HO-Tryptamine (serotonin)&lt;br /&gt;
* 1.3 - 5-HO-DMT N-oxide (Bufotenine N-oxide)&lt;br /&gt;
* 1.6 - 5-HO-DMT (bufotenine)&lt;br /&gt;
* 1.7 - N-Methylserotonin&lt;br /&gt;
* 1.7 - DMT N-oxide (Dimethyltryptamine N-oxide)&lt;br /&gt;
* 1.7 - 5-MeO-NMT (5-Methoxy-N-methyltryptamine)&lt;br /&gt;
* 1.7 - 2-Methyl-1,2,3,4-tetrahydro-beta-carboline&lt;br /&gt;
* 1.8 - NMT (N-Methyltryptamine)&lt;br /&gt;
* 1.9 - 5-MeO-DMT (methoxybufotenin)&lt;br /&gt;
* 1.9 - Tetra−Hydro−Harmine (THH)&lt;br /&gt;
* 2.0 - DMT (Dimethyltryptamine)&lt;br /&gt;
* 2.5 - Harmine&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Alkaloid XlogP3 list'''&lt;br /&gt;
&lt;br /&gt;
* -1.4 - Muscimol&lt;br /&gt;
* -1.6 - Psilocybin&lt;br /&gt;
* 0.6 - Harmalol&lt;br /&gt;
* 0.7 - Mescaline&lt;br /&gt;
* 1.2 - Harmaline&lt;br /&gt;
* 1.2 - Bufotenine&lt;br /&gt;
* 1.5 - 5-MeO-DMT&lt;br /&gt;
* 1.6 - LSA (ergine)&lt;br /&gt;
* 1.8 - Gramine&lt;br /&gt;
* 1.9 - Tetrahydroharmine&lt;br /&gt;
* 2.0 - DMT N-oxide&lt;br /&gt;
* 2.1 - Psilocin&lt;br /&gt;
* 2.1 - NMT&lt;br /&gt;
* 2.5 - DMT&lt;br /&gt;
* 2.5 - Salvinorin A&lt;br /&gt;
* 2.5 - Elemicin&lt;br /&gt;
* 3.5 - Voacangine&lt;br /&gt;
* 3.6 - Harmine&lt;br /&gt;
* 3.6 - Harman&lt;br /&gt;
* 3.9 - Ibogaine&lt;br /&gt;
&lt;br /&gt;
Lower XlogP values are more water soluble, and higher XlogP values are more non-polar soluble.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Solvent XlogP list'''&lt;br /&gt;
&lt;br /&gt;
* -0.7 - DMSO&lt;br /&gt;
* -0.5 - Methanol&lt;br /&gt;
* -0.1 - Ethyl Alcohol&lt;br /&gt;
* 0.2 - Acetone&lt;br /&gt;
* 0.4 - IPA&lt;br /&gt;
* 0.4 - MEK (Methyl Ethyl Ketone)&lt;br /&gt;
* 0.7 - Ethyl Acetate&lt;br /&gt;
* 0.9 - Ethyl Ether&lt;br /&gt;
* 1.5 - DCM&lt;br /&gt;
* 2.1 - Chloroform&lt;br /&gt;
* 2.5 - Toluene&lt;br /&gt;
* 2.5 - Xylene&lt;br /&gt;
* 3.7 - Limonene&lt;br /&gt;
* 4.3 - Heptane (similar to naphtha)&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Known_substance-interactions_and_their_effects</id>
		<title>Known substance-interactions and their effects</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Known_substance-interactions_and_their_effects"/>
				<updated>2013-11-24T01:43:32Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* DMT + Mushrooms (psilocybin) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{ShowInfo|[[Image:Error.png]]|'''WARNING:'''|'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
This article is about the interactions and effects of  mixing different entheogens, both with each other and with medicine. Some combinations have a good synergy while others can be a DEADLY combination! Taking any substance carries a high responsibility, please read the WARNING section with great care!&lt;br /&gt;
&lt;br /&gt;
== Warning! ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: orangered;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&amp;lt;br /&amp;gt;&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: red;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Even though the interactions of certain substances are described here, it is extremely important to be safe at all times! This article is only to give information about interactions and their effects, '''this article is NOT meant for advice on taking any combination!'''&lt;br /&gt;
&lt;br /&gt;
Many interactions described here are ''subjective descriptions'', so what is shown here is only an ''indication'' on how certain combinations can affect you and how safe they are. Many times those effects are dependent on dose (of each substance), route of administration, timeline of administration, set and setting, your mood, your physical health, your mental health and many other factors. &lt;br /&gt;
&lt;br /&gt;
== Psychedelics ==&lt;br /&gt;
&lt;br /&gt;
=== DMT ===&lt;br /&gt;
&lt;br /&gt;
Some report dysphoria at lower doses. I (House) do not find this to be the case I find low doses incredibly euphoric. Higher doses can be known to go beyond human emotions and concepts. Higher doses of DMT are also known to cause strange bodily hallucinations like the feeling that you have stopped breathing, or that your heart has stopped beating. These hallucinations are common and can be countered with conscious relaxation and meditation prior and during the experience. You do not have to submit, per se, but beware that you may have to let go of certain intensities during the experience. It can easily be the most &amp;quot;intense&amp;quot; experience of your life for some people, and this is *NOT* a bad thing!&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DMT + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Harmalas (MAOI)|#406040|#60FF60|OK|[[Harmalas]] potentiate and prolong the effects of [[DMT]], while at the same time it adds a slight psychedelic effect of it's own. For DMT to be orally active, a [[MAOI]] is mandatory.|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Oral activation. Potentiation. Slowed-down effect. The two go hand in hand creating a perfect synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DMT + Mushrooms (psilocybin) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DMT + Mushrooms (psilocybin)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Another profound synergy that seems to unlock the potential of the [[mushroom]]. Either @ peak or after.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Positive.png]]|When DMT is smoked at the peak or post-peak of mushrooms, there is an extreme synergy that can make it for an incredible experience that can take one very very far! My favourite combo}}&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized DMT whilst on mushrooms- Potentiation, intense synergy between the two tryptamines, very strong visuals came thick and fast.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== DMT + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Negative.png]]|I didnt like it at all because it felt like LSD acts as an anchor and holds one down, preventing breakthrough}}&lt;br /&gt;
}}&lt;br /&gt;
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==== DMT + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Euphoric, not as deep of a trip, but there is zero anxiety present which can be useful and awesome in it's own right.}}&lt;br /&gt;
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==== DMT + Mescaline ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Mescaline|#406040|#60FF60|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy here. Potentiates the [[mescaline]] and smooths it out.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Neutral.png]]|The mescaline seems to 'dull' the [[DMT]]. So there was not as much effects from smoking the DMT on Mescaline as you would expect.}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Negative.png]]|The mescaline seemed to hold the [[DMT]] towards the center of the vision, as if it didnt let it &amp;quot;expand&amp;quot;. I saw the DMT visuals curling up, like as if a magnetic/gravitational force didnt let it happen freely. The trip felt weird, it didnt feel 'natural' or 'flowing' to me. Tried it twice in different occasions to similar results and didnt feel like it's a good combination for me}}&lt;br /&gt;
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==== DMT + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Alcohol|#805000|#E0A040|SAFE But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|I find that combining the spice with a carcinogenic neurotoxin like [[alcohol]] completely negates the experience and masks it with toxic nullification (Yes, I am quite biased)}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The alcohol did  have a negative impact on me. I tried to drink a few beers beforehand to mitigate the anxiety of the [[pharmahuasca]] but that only resulted in dulling down, confusion and nausea.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|The Spice doesn't like Alcohol, you'll either wont remember or get a bad vibe.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== DMT + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK, although some people don't like it. If you are a daily cannabis smoker it shouldn't be a problem, but if you get anxiety from using [[Cannabis]] occasionally it may be wise not to mix it with [[DMT]].}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:neutral.png]]|If I smoke DMT / Changa 1-2 hrs after my last hit of cannabis it is great, if I smoke DMT &amp;amp; Cannabis together it is not so great.}}&lt;br /&gt;
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==== DMT + Dissociatives ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Dissociatves|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|By far my absolute favourite combination. This experience is equal in intensity as DMT but without the ego loss. An entirely new realm all together where YOUR controller. This can mean many things, its sheer awesomeness with seemingly no downside gives it quite an addictive quality. During my first encounters with this combination I probably went through more DMT in one night then I normally would have in months, maybe a year.}}&lt;br /&gt;
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=== Harmalas (MAOI) ===&lt;br /&gt;
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Side effects include contraindication with certain substances. Make sure you understand interactions with substances before using them! At higher doses users experience nausea and vomiting, but this also isn't necessarily a bad thing, since harmalas are anti-parasitic, purging is often considered cleansing to both the body and the mind. Chest pressure is also common with ayahuasca. Feelings of having something heavy sitting on you. This is normal and if experienced just relax and let it be, it's part of the serpents coil.&lt;br /&gt;
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==== Harmalas (MAOI) + Caffeine ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + caffeine|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally don't mind a low dose of harmalas on top of caffeine, it can counter act the sedation from the harmalas in the right dosages. Too much of both and you will experience uncomfortable heart rate. So new users to this synergy take caution and start low!}}&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|I had one cup of average strength coffee about 2 hours after smoking changa and I got very edgy and nervous. Coffee barely even wakes me up but I was wired for about an hour. Quite uncomfortable.}}&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|For me, a cup of yerba matè plus ayahuasca equals awful experience. There seem to be some people who can't take caffeine and ayahuasca}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + 5-MeO-DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + 5-MeO-DMT|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|this could be hard on some metabolism, or dangerous, but IME, a great form of pharmahuasca, more nausea than with N,N-DMT, but also more euphorie.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Neutral.png]]|Harmalas will significantly increase potency of 5-MeO-DMT. 40-60mg harmaline + 10mg 5-MeO-DMT orally is equivalent to 30-35mg oral 5-MeO-DMT by itself or 10 mg intranasally (see Ott 2001 Note that 35mg by itself was not active dosage to shulgin but was for ott}}&lt;br /&gt;
{{UserDescription|Picatris|[[Image:Negative.png]]|Potentially unsafe combination and health risks due to metabolic issues. For more info search the forum for the thread titled &amp;quot;Does Anyone Here Eat 5-MEO-DMT?&amp;quot;.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Harmalas (MAOI) + Kava kava ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + Kava Kava|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
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==== Oral Harmalas (MAOI) + Opioids ====&lt;br /&gt;
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{{SubstanceInteraction|Oral Harmalas (MAOI) + Opioids|#604040|#FF6060|BAD IDEA!|Has the potential for adverse reactions, namely CNS excitation or depression (resulting in high or low blood pressure).|&lt;br /&gt;
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==== Oral Harmalas (MAOI) + L-dopa ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + L-dopa|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|taking levodopa with MAOIs runs the risk of a hypertensive crisis and levodopa should not be taken for at least 2 weeks after MAOIs; the risk of taking RIMAs (specifically moclobemide) with levodopa is one of increased side effects which include anorexia, nausea, vomiting, agitation, postural hypotension, tachycardia, arrythmias, hypomania, psychosis, depression, headache, flushing, gastrointestinal bleeding, itching, rashes, abnormal involuntary movements. &lt;br /&gt;
&lt;br /&gt;
The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinations}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + tyrosine ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + tyrosine|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|l-tyrosine taken with MAOIs renders it more likely to be a vasopressor ie cause an elevation in BP.&lt;br /&gt;
&lt;br /&gt;
The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinationss}}&lt;br /&gt;
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==== Harmalas (MAOI) + Dissociatives ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas (MAOI) + Dissociatives|#604040|#FF6060|BAD IDEA!|Even though there are reports on the net of people combining MXE with harmalas, in the right dosages harmalas + dissociatives have the potential to cause cardiac arrest.|}}&lt;br /&gt;
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=== Mushrooms (psilocybin) ===&lt;br /&gt;
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I (House) think the most common side effect I hear about with shrooms is stomach discomfort. A lot of people don't know that you really are not supposed to consume any kind of raw mushroom. It's a rare case in the culinary and medicinal fields where raw mushrooms are told to be ingested. (I can think of a few exceptions, of course.) So for some ingesting the raw material can be very nauseating, myself included. Making a tea or the lemon tek is the way to go. By soaking raw mushrooms in lime juice, the citric acid literally cooks the mushrooms breaking down the cell walls. This is also known as a ceviche in the cooking world. Personally I just slip the shot of lime juice with the mushrooms in it back, it tastes good and I don't experience nausea this way. Some people filter out the mushroom material from the solution. Experiment. Taking too many mushrooms can lead to a feeling of being poisoned, but as far as I know no one has ever died from taking them on their own. Dose accordingly!&lt;br /&gt;
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==== Mushrooms + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I won't use mushrooms without cannabis; Noticeable synergy and eases any anxiety present. Some people who don't use cannabis often find that this combo causes paranoia.}}&lt;br /&gt;
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==== Mushrooms + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Profound synergy. Great for meditation and dance}}&lt;br /&gt;
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==== Mushrooms + Harmalas (MAOI)====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Harmala (MAOI)|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love the harmala + mushrooms synergy, but some have noted that the harmalas potentiate the mushrooms very much and have had rough trips! If you want to experiment with this combo, start low and work your way up!}}&lt;br /&gt;
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{{UserDescription|Mindlusion|[[Image:Neutral.png]]|I tried this combo at a fairly high dose, it GREATLY potentiated the effects.. And I absolutely loved it, quite more then the intensity I was looking for. Although after the first 6 hours, I felt the trip had come to conclusion, I was ecstatic, but physically and mentally exhausted, only to have the experience continue at practiaclly the same intensity for ANOTHER 6 hours. Before I could get any sleep whatsoever.  If you try this combo, its great, just be prepared to trip for a LONG time.}}&lt;br /&gt;
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==== Mushrooms + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Alcohol|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, slower than cocaine however. Also, people tend to get negative from this combo. One might hypothesize that alcohol tends to turn the trip in a darker direction.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad idea, high chances to end up puking and feeling miserable.}}&lt;br /&gt;
{{UserDescription|Frankycou|[[Image:Negative.png]]|This is potentially very unsafe! some type of mushroom are known to develop poison when mixed with alcohol. This is very rough information that I am reporting since I don't remember the exact text and source but basically I read from a reputed source that some types are EXTREMLY BAD  to mix and should be avoided at all cost.}}&lt;br /&gt;
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==== Mushrooms + Alcohol + Cocaine + MDMA====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Alcohol + Cocaine + MDMA|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad bad idea. I took the MDMA, Coke and Alcohol at the end of a Shrooms trip. Anxiety and profound guilt were felt in my whole body}}&lt;br /&gt;
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==== Mushrooms + Cocaine ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Cocaine|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, or even stop it dead in it's tracks.}}&lt;br /&gt;
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=== LSD ===&lt;br /&gt;
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LSD is a potent vasoconstricting substance. This means it causes an increase in blood pressure by tightening the blood vessels in the body. This can be countered with vasodilating substances. Some find that oral hash completely diminishes the vasoconstriction. I like using transdermal magnesium prior to a dose to also help with things like jaw tension. Also, conscious relaxation, deep breaths, and massage (even done by the self) can help curb tension experienced from the drug. If you feel over stimulated or uncomfortable, you probably need to &amp;quot;Flow&amp;quot;, so to speak. Get up, stretch, dance around, laugh, have an orgasm, be creative, play a musical instrument, take a hot shower. Things like this help with getting energy flowing and making meditation easier. Eat a bit of fruit on the come-up if you feel some unease! Many people find cannabis greatly eases the transition, but of course not everybody. &lt;br /&gt;
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==== LSD + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
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==== LSD + Ayahuasca + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Ayahuasca +DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is my favorite synergy of all time. First take the LSD, then take a comfortable dose of banisteriopsis caapi tea, then smoke as much DMT/Changa as you desire. Absolutely astonishing.}}&lt;br /&gt;
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==== LSD + Mushrooms ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mushrooms|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A lot of people don't like this combination for some reason- both drugs are just so powerful they may not need to go together, with that said however some people like the combo and it is OK to take.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy with Psilocybe mushrooms.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|I took the Mushrooms while coming down from the LSD and I didn't feel any effect whatsoever. (EDIT: You probably have to take lots of Shrooms to fight the tollerance)}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I haven't experimented enough with this combination to say for sure. Only very small doses, and they were kind of hazy.}}&lt;br /&gt;
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==== LSD + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Classic Combo. Take at the same time or let the acid kick in then take the MDMA. Profound synergy!}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDMA gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|MDMA and LSD together is one of the most amazing synergy in terms of dancefloor experience...}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|The only time I did it, I took the LSD a while after the MDMA. Everything was very smooth and shiny. Great dancing combo!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|&lt;br /&gt;
MDMA removes any negative experiences I feel with LSD. POWERFULLY beautiful combination! All aesthetics are increased 10x, music is beautiful and flowing, playing music is amazing, dancing is amazing. Cuddling, hugging, telling people you love them... yes, this is a winner.}}&lt;br /&gt;
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==== LSD + MDAI ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDAI|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDAI gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
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==== LSD + Mescaline ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy but it's hard to tell how each drug is affecting each other. A bit like LSD + MDMA but a deeper, so to speak.}}&lt;br /&gt;
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==== LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Cannabis vasodilates the vasoconstriction of LSD especially if taken orally. Potentiates and smooths out the trip. Great for daily smokers. Has been known to cause anxiety in those who don't use Cannabis too often.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|I almost never use [[cannabis]], I wanted to use the cannabis versus the stimulation of the LSD. It gave me more visuals but it also made me dizzy. Overall I did not like it.}}&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|Definitely has led to a bunch of paranoia at times (I'm prone to that with weed alone though) but if combined carefully it can be totally worth it although i never do it anymore (no lsd). If a large amount is smoked at the peak-especially if i have a low tolerance- then it can really catapult the experience into a sort of out of body type thing with full blown 3-d immerse visions, IME}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|It gives a bit of anxiety, although the effect of LSD is potentiated for a little while. Be aware, it's very hard to roll a spliff while tripping }}&lt;br /&gt;
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==== LSD + Cannabis + Tobacco====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I mostly smoke spliffs, but I find spliffs (a 50/50 mix of cannabis and tobacco) To be quite pleasant at all periods of the LSD comeup. Usually my physical form is quite shakey and or cold during the LSD comeup, and cannabis warms me up and calms down any tension or shakiness. Spliffs induce a deep trance state for me, very pleasant.}}&lt;br /&gt;
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==== LSD + MXE ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Aetherius Rimor|[[Image:Negative.png]]|Did 30mg of [[MXE]] in the 2nd hour of 2 hits. That's the only time I've not been at home and unable to verbalize/coordinate movement. Luckily that's what designated drivers are for! Won't combine them again. Definitely stronger effects than same dose of each independent of each other.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The MXE potentiates the [[LSD]] effects with more visuals but it also significantly alters motor function to the point of immobility at high doses.}}&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Radical and profound potentiation/synergy. 12+ hour trip and much longer to sleep. I really love the synergy of LSD+MXE but I'm the kind of person who naturally chills during a trip, so being pancaked by effects is just an extra plus for me.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|I have tried this combination many times, but only at high doses of MXE, I loved this combination, it intensified and increased the depth and power of the dissociated 'hole' while making it easier to bring back more from the experience. The only negative effects Ive felt is the dissociated 'whobblies' that last for an hour or two after the hole, which can be annoying while trying walk around on LSD. In my experience, it is best taken early in the LSD trip, when the effects subside you are usually at the LSD peak, this also seems to ease any anxiety. (I would also like to mention I am quite mobile at high doses of MXE while on LSD, only after mobility can be hindered by the drunken like 'whobblies')}}&lt;br /&gt;
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==== LSD + Amphetamines ====&lt;br /&gt;
{{SubstanceInteraction|LSD + Amphetamines|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:neutral.png]]|Somewhat safe but...Makes the LSD less visual and a bit more difficult to handle mentally because of the stress caused by the stimulants. It can be an interesting mix if partying but I would try to avoid it if possible. At least try to get pharmaceutical grade stimulants and not dirty street pills.}}&lt;br /&gt;
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==== LSD + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Harmalas (MAOI)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|You MUST make sure you have pure LSD, however! You do not want to mix harmala (RIMA, MAOI) with an unknown drug laid on blotter. It's great taken with a dose or taken after the dose has kicked in, as the vasodilation of the harmala counters the vasoconstriction of the LSD.}}&lt;br /&gt;
{{UserDescription|Enoon|[[Image:Neutral.png]]|Super strong synergy, stronger than usual visuals, visions, OBE, but also nausea, imobility and substatial amount of apprehension}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy/potentiation, first timers should take very small doses to see how they react and only raise gradually.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I must admit I'm a bit of a Harmala &amp;quot;fiend&amp;quot;. I love them and I see no negative applications to them, pretty much, as long as you are physically safe. They potentiate the visuals of LSD, get rid of the shakes and nervousness, help me emotionally sort through things and make me warm and content and happy. This is a WINNING combination, especially with chocolate caffeine or spliffs. all very good in my books. Great for meditation, dancing, writing, drawing, or playing music.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== LSD + Amanita Muscaria/Pantherina ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Amanita Muscaria/Pantherina|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Great synergy, tends to make the trip more challenging and more visionnary, more entheogenic also, but it is again harder than LSD on it's own.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== LSD + Alcohol====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Mescaline|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|Doesn't make sense to me to combine a CNS depressant with the brilliant effects of LSD.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Great and jolly, but it makes the trip a bit blurry and less powerful. Don't over do it, your liver wont appreciate it!.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't enjoy alcohol in general, so I'm slightly bias. When I was younger (15-16) I would shotgun beers on LSD and that was quite nice, but any hard alcohol combined with LSD turns you into a flailing, falling idiot apologizing for making such a big mess.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== LSD + GHB====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + GHB|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't have enough concrete experience with this combination, but I haven't experienced negative interactions the few times I have done them. the GHB is very warm and mellow, although a bit of nausea or headache or spinny-ness can occur at higher doses, if everything is kept moderate it is much more pleasant than alcohol, although not quite as pleasant as MDMA.}}&lt;br /&gt;
}}&lt;br /&gt;
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=== Mescaline ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Mescaline is a phenethylamine that does not have an amphetamine group on the molecule, unlike MDMA. This allows it to be able to be used with harmalas without contraindication. A very gentle and long lasting psychedelic with great empathic and stimulating properties. &lt;br /&gt;
&lt;br /&gt;
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==== Mescaline + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A great way to potentiate your mescaline dose is with caffeine, especially coffee. Yerba mate and other teas are good too. Even the days after a trip, a nice cup gets you right back in that lovely state-of-mind. Some may find this combo too stimulating, however. The coffee can also be used to get digestion flowing if you are having indigestion from the cactus.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Noticeable potentiation and takes the edge off the stimulation subsequently. These two go hand-in-hand if you are a regular cannabis user. If not, start low!}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + Harmala|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|No contraindication here. A nice synergy. The harmala takes away some of the stimulation of the mescaline and makes the experience more dreamy. }}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|You can drink a lot of alcohol on mescaline, but I don't see the point. Takes away from the profound effects of the psychedelic.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|In high doses it's extremely confusing! Good chances to blackout and puke. }}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Nice combo, but it wasn't enough to understand its effects.}}&lt;br /&gt;
}}&lt;br /&gt;
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=== Iboga ===&lt;br /&gt;
&lt;br /&gt;
Careful with this one! Much research and tests must be done before ingesting this substance. It is clinically proven to slow down a rhythm of the heart beat and has killed people because of this. A heart panel and EKG are common tests preformed before ingesting this substance. Please beware of this and do a lot of research before even considering this very profound medicine! Side effects include disorientation, immobility, nausea, in high doses for very long periods of time. Some people still can't drive a car 1 week after a flood dose, for example.&lt;br /&gt;
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==== Iboga + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|LSD becomes much more potent after Iboga and I would suggest taking it sometime between 1-7 days after taking a low dose of Iboga. For me I find that the LSD really puts the teachings of the Iboga into perspective. Be careful though, there is a definite potentiation.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:negative.png]]|very challenging in my experience so the LSD was probably very high (vial wash) with loads of noribogaine (2 grams RB every days for four to five days) in the system. I personnally wouldn't recommend it.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Mushrooms ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I find that psilocybe mushrooms are a really great synergy. They seem to kick in the Iboga about 3x as hard, so a low dose of both makes for a good journey. Euphoric, meditative, deep combination. Great for sorting things out in your life.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with Iboga and cannabis. Noticeable potentiation. Also takes care of the intense nausea with higher doses of Iboga a bit. I believe this synergy is even used traditionally in some instances.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Iboga and canabis are great together, the iboga focus the train of thought from canabis while canabis relax the iboga (stimulant at low doses) experience.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Iboga + Harmala|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|While myself and others have found a low dose of harmala to be a nice synergy with Iboga, others have found the combination too intense. Start low and work your way up.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:positive.png]]|Iboga and harmalas must be treaten with caution though in low doses, it seems like a very good combo though questionnably safe (in regards of mixing RIMA and SSRI).}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Coffee ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Iboga + Coffee|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love a low dose of Iboga with a good cup of coffee, and cannabis. I find it stimulating both physically and with the clarity of mind. Some may find this too stimulating. Don't expect to sleep the night of taking this combo!}}&lt;br /&gt;
}}&lt;br /&gt;
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=== MDMA ===&lt;br /&gt;
&lt;br /&gt;
The most common side effects of MDMA are jaw tension, feeling burnt-out the next day, and it's minimal amount of neurotoxicity.&lt;br /&gt;
A lot of people &amp;quot;pre load&amp;quot; with substances that are neuroprotectant before, during, and after the experience. Neuroprotectants include cannabis, nootropics, vitamin C, 5-HTP, and others. Jaw tension can be countered again with transdermal magnesium, conscious relaxation, meditation and massage. As for feeling burnt-out, try to only redose a small amount one time or not at all. Constantly redosing can cause more burnout srensations. Also dosing too high. You might want to touch, hug, kiss, and tell how much you love everything around you, too.&lt;br /&gt;
  &lt;br /&gt;
Taking MDMA with MAOI and certain prescription medications can lead to seratonin syndrome and even death so plesse be careful!&lt;br /&gt;
&lt;br /&gt;
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==== MDMA + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + Harmalas (MAOI)|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with MDMA and cannabis. Smooths out the stimulation. Biologically speaking, the cannabis actually works as a neuroprotectant against the neurotoxicity of MDMA. They go hand-in-hand if you are a fan of cannabis!}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Very nice, but you end up smoking way too much.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== MDMA + LSD + Ketamine + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + LSD + Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Better than OK for me. Have had some of the best nights of my life with this cocktail.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + DMT + Ketamine ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + DMT + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Out-of-this-world OEVisuals. The euphoria of the MDMA is present and the visual quality of the K synergizes with the DMT in a very strange way. I would suggest taking only small dosages with all of those three if you are to give this combo a try.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== Ketamine ===&lt;br /&gt;
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==== Ketamine + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is a pretty classic and noteable synergy that many people love. The K takes you very deep into yourself, and away from yourself at the same time.}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. Similar to the 2CB combo, be careful, both of these drugs have a tendency to be a bit mind bending, and in combo, expect it to get wild!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|LSD + Ketamine is definitely a strange combination. In my experience it lends itself to meditation because alot of the time the mind is too befuddled to properly draw a train of thought. I find this combination quite inarticulating, it's one of the few drug interactions that make me a bit of a &amp;quot;dumbass&amp;quot;, and just puddle me on the floor. Lower doses of ketamine + lsd are good for dancing, higher doses, for trancing.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Love it!}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. You will get lost in the deepest recesses of your mind for quite some time, I love comatose tripping, but it isn't for everyone.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Harmala|#604040|#FF6060|BAD IDEA!|Harmalas are contraindicated with dissociatives, this means you do not want to combine them. At high doses the cardiovascular system can shut down.|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|Made the mistake of trying changa on top of LSD + K once and I will never do that again. Intense bronchial constriction and chest pain was noted.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Ketamine + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coming back from the ketamine trance and smoking cannabis. Great for meditation and integration if you enjoy cannabis!}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|DMT on Ketamine is out of this world stellar. The dissociative properties of ketamine completely eliminate any anxiety present, and the two work together to take you deep into whatever it is that we are...}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Some people suggest ketamine may smooth the entry int tryptamine space and some report incredible experiences. Special care is needed with ketamine due to it's potentially addictive nature and due to being dissociative/anaesthetic and increased risks of physical accidents. Justin Case's best results have been reported when k dose is kept low and tryptamine dose is solid but not excessive.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|This combination is grandeur, extremely powerful. I agree with both House and Endlessness, especially about the addictive part. Extensive use of the this combination and other DMT + Dissociatives, seems to make a preexisting addiction worse. It's a lot of strain on ones psyche to abuse this combo.) }} &lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + LSD + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Throwing DMT into the mix is just that much more powerful.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|^ What House said.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Some people love it, I don't. I don't like small bumps of K, so when I take it, it always end up taking over all the rest.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|I heard it's not very safe. I did it few times and the day after I always felt miserable.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
===Salvia Divinorum===&lt;br /&gt;
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==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|OK. can be extremely disturbing though or unbelievably profound and real.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Salvia + Changa + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Changa + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is probably my favorite mix. I've had some of my deepest experiences mixing these three including one with multiple breakthroughs one on top of the other cascading deeper with a new universe created and destroyed each time.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Salvia + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Salvia + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is a very therapeutic anesthetic. This kills pain very well and leaves me in a dreamy visionary state without the mind warping dissociating effects that salvia has on its own. As long as you don't go heavy on the salvia! }}&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good! Great way to take the edge off of the pre-flight anxiety for salvia, which can be pretty rough at times.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Effects are dramatic but its not clear if there is synergy or more like additive effects. }}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
== RC's ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 2C-B ===&lt;br /&gt;
&lt;br /&gt;
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==== 2C-B + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-B + Ketamine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Have seen 2 people lose the plot on this combo, so be careful. For me, it subdues the edginess of the phenethylamine buzz, while adding a trippy colourful edge to the Ketamine. Can get confusing, which I think was why people freaked out a bit.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== MDMA + 2CB + K + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + 2CB + K + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Similar to the above, moar euphoria, but again please be careful with dosages.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== 2C-I ===&lt;br /&gt;
&lt;br /&gt;
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==== 2C-I + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-I + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:negative.png]]|made me feel sick, smoking anything on 2CI wasn't nice.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== MXE ===&lt;br /&gt;
&lt;br /&gt;
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==== MXE + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MXE + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. deep, visual, introspective, make sure you don't have anything to do / people to entertain as chances are you will be lost in thought. Did experience a little muscle tremoring, but less than 2CI on its own.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== 5-MeO-DALT + MXE ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|5-MeO-DALT + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|While on ~50mg 5-MeO-DALT orally I did a little test bump of 15 mg MXE insufflated and within minutes felt my heart rate go up and felt very dizzy. Thought that I had finally done it and mixed the wrong stuff and I would have to go to the ER but it stopped escalating and I just waited it out.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 25i-NBOMe ===&lt;br /&gt;
&lt;br /&gt;
==== 25i-NBOMe + Cannabis + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|25i-NBOMe + Cannabis + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|billydgator|[[Image:Positive.png]]|Awesome! About 2.5 hours into an 25i nbome trip i took some small blasts of spice, brought me from ++ to ++++.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== AM-2201 ===&lt;br /&gt;
&lt;br /&gt;
==== AM-2201 + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|AM-2201 + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Nice high, feels good and very sedating, very happy and relaxed. But can be VERY hallucinogenic, only smoke a little! Bizarre and realistic and gory hallucinations (man with half a leg bleeding allover the place!) are possible, voices become distorted and merged and speak impossible ridiculous things. The hallucination is short lived.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== MDAI ===&lt;br /&gt;
&lt;br /&gt;
==== MDAI + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDAI + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized hits of DMT seem harder to break through on, but the effect of the DMT seem prolonged. Strange visuals (small pinpoint kaleidoscope patters appear and dissappear), last for longer than the spice effects would last, by up to 25 minutes longer. Does not seem dangerous, but the fact it makes open eye visuals linger for so long is interesting...}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Medicine ==&lt;br /&gt;
&lt;br /&gt;
=== SSRI/SSRE ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Cannabis ===&lt;br /&gt;
&lt;br /&gt;
Cannabis works as a potent anti-inflammatory and vasodilating medication. Those who use it often find that it goes well with almost every other drug, while those who seldom use it may find that when combined with psychedelic substances it can cause paranoia and uncomfortable potentiation. If you are unfamiliar with the ways cannabis synergizes with other substances, it is wise to start low and work your way up to a comfortable amount. Many find that oral cannabinoids act as a more potent vasodilator than smoked, making this a good option for countering the vasoconstriction of drugs like LSD and LSA. Many people also use cannabis to counter the nausea caused by other drugs. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Cannabis + Harmalas (MAOI) ====&lt;br /&gt;
{{SubstanceInteraction|Cannabis + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:positive.png]]|Harmalas potentiate the effects of cannabis, adding a nice dreamy feel and tracers to the vision. Since they are both vasodilating compounds, some people experience headaches if combined in high doses. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Other ==&lt;br /&gt;
&lt;br /&gt;
=== Nootropics/Piracetam/Aniracetam ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Piracetam + Psychedelics/Amphetamines ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Piracetam + Psychedelics/Amphetamines|#805000|#E0A040|OK but|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Trout notes that justin case, toad and others have reported substantial increase in potency of phenetylamines (such as MDMA, mescaline, amphetamines) and suggest dosage is halved. Possible potentiation of tryptamines too. There is very little data on the pharmacodynamics and toxicity of this mixture, so care is adviced, even though due to low toxicity of tryptamines and piracetam by itself, its possible the toxicity of mixture is also low.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== LSD + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I have been dosing piracetam daily for a few weeks now, and in that time I've done LSD twice. Definitely noticed that each time the piracetam VASTLY improves ability to articulate myself, ability to recall the trip and get into deeper meditative states. Piracetam also greatly helps my ability to write more clearly in my journals, improves my ability to play music and LSD enhances my musical creativity. All in all, very good combination.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Caffeine + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Caffeine + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dream Weaver|[[Image:Positive.png]]|I occasionally dose piracetam anywhere from 800mg to 4 grams ingested on an empty stomach (dissolved in water). I find the synergy of caffeine + piracetam to be quite soothing. It is important not to ingest too much caffeine or an anxiety like feeling will occur/stomach problems... Mostly positive if done right. Effects are very soothing and uplifting. Make the most mundane task entertaining. You become quick and sharp as a whip. Somewhat similar to 30mg xr adderall + 5-15mg valium. Great combo! Ideal for mornings!}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Kava Kava ===&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava kava is relaxing and aids in dissipating pre-flight anxiety. A warm cup is great after DMT insufflation or vaporization. There is a noticeable synergy between the two and no discomfort or side effects have been noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + LSD ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava Kava after the peak of LSD when it's wearing off is a great way to take the edge off and get some rest. It's very effective and enjoyable this way with no side effects noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy. Very relaxing.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== DXM ===&lt;br /&gt;
&lt;br /&gt;
==== DXM + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|Great. Visually incredible. Cannabis at peak enhanced visuals even further. Use more mushrooms than DXM.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DXM + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good. Great way to up the psychedelic aspect of dex.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Tobacco ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Great. Dex really makes tobacco shine, brings out the best world of nicotiana.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + NO2 ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + NO2|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Very, Very intense. Too much for some people, but for others, euphoria.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + HBWR (LSA) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + HBWR(LSA)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|It really increases the psychedelia of dex, brings some awesomely colorful visions, but be very careful. Not much is known about the interactions of these two. I would not go above 3 HBWR seeds in combo.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + DMT ====&lt;br /&gt;
{{SubstanceInteraction|DXM + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|One of the most intense experiences I could possibly imagine. Classic Dissociative + DMT, but incomparable at the same time, I could say I like this combination better then DMT + Ketamine, or DMT + MXE, but its incomparable.  It dissolves any preflight, or during anxiety whatsoever, the utterly intense godly power of DMT is given to YOU. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Chocolate/Theobromine ===&lt;br /&gt;
&lt;br /&gt;
Theobromine, a methylated xanthine found in chocolate and yerba mate, is a stimulant and psychedelic potentiator.&lt;br /&gt;
&lt;br /&gt;
Low doses combined with psychedelics causes noticeable potentiation and empathy.&lt;br /&gt;
High doses have the potential to cause nausea and over stimulation, so start low and work up to a comfortable dose!&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Aka The Mocha. Nice warm fuzzy sociable synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Definite potentiation and synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Passionflower ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Passion Flower|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:neutral.png]]|OK, but don't use a lot of theobromine. I have had psychedelic effects with this combination, but also intense nausea and bronchial-constriction at higher doses.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK but do not use a lot of theobromine or harmala. A little goes a long way! Same thing goes here if you have a little too much of either theobromine or harmala expect nausea and vomiting. At appropriate doses however the synergy is very nice. Theobromine potentiates the harmalas and any psychedelics you take as well.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I haven't experimented too heavily with eating cacao on LSD, but I usually eat one or two handfulls of raw cacao nibs. I found the stimulation synergistic, very good for walking or running through the forest. I found that the cacao gets rid of the &amp;quot;shivers&amp;quot; I experience from LSD and warms me from the inside.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Kratom ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kratom + MXE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kratom + MXE|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Effects: Like 10-15 mgs of Hydrocodone.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== NO2 ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|NO2 at peak of a mescaline trip was incredibly euphoric. Felt like psychedelic MDMA.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + DMT ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|When nitrous is inhaled immediately after dmt, its reported by some people to significantly enhance the experience.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|OK. Very powerful. Be prepared to lie down and be somewhat paralyzed, depending on dosage.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Amazing visuals. Out of body experience, very comfortable but no contact at all with the body.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Amazing! For few minutes you are in a DMT like world. (I'd love to try LSD + NO2)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Alcohol (Ethanol) ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:neutral.png]]|I have done this a few times and been safe, but I was very careful and spaced my drinks out. I have read horror reports of people drinking to much on dex, and puking for upwards of an hour or two.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Negative.png]]|Puke city.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:negative.png]]|Another potential Show Stopper. The Alcohol really tends to lessen, dull, or end the effects of the mdma. Aside from that, there is the danger of dehydration--when you are rolling you should drink water.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Quite nice, but do not over do it! If you have been drinking too much, you'll be hit by a train when the MDMA comes down.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Bufotenine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Bufotenine + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Not a good combo. The Bufotenin's nausea will probably make you puke and the Alcohol will diminish the Bufotenin visual effects.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Caffeine ===&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Caffeine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|Not so good. Caffeine disturbs the mushroom flow.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coffee or yerba mate with LSD. Wonderful combo.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I'm a bit of a coffee / mate junkie, so I find the combination quite synergistic. Smoking a spliff and drinking coffee on LSD makes me feel like all is right in the world and I can sit in meditation and take a good 30 minutes to drink my coffee and have my smoke. It lends itself to visual enhancement and incredible tingling sensations in the body, which for some people could make them quite restless, but I enjoy meditation on stimulants.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Melatonin ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Melatonin + Mushrooms + Harmala + Cannabis + Changa ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Melatonin + Mushrooms + Harmala + Cannabis + Changa|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|50-100mg melatonin (very meditative and harmala-esque for me. Combines well with others like a mind lube. A few hours later - lower dose of oral harmalas (preferably caapi) + mushrooms + smoked Cannabis + changa to top it off and push it all through. Amazing synergy. Need to balance the ratios accordingly though. You can leave out the melatonin if your not used to higher doses (they're not really that sleepy like the lower doses though, oddly). I prefer this combo after a day or to without sleep. Sleep deprivation is a powerful means of accessing altered states that's been used for thousands of years, like in the epic of Gilgamesh, for example. That's not for everyone though and works best with a raw, plant based diet.)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Benzos/Barbituates ===&lt;br /&gt;
&lt;br /&gt;
Benzodiazepines can be reduce an agitated rough/unpleasant trip but are generally not recommended if other non-invasive supportive care-taking can be done, because these substances will dull the consciousness and might prevent the tripper from learning from the hard experience and integrating it.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Chlorpromazine + Psychedelics ====&lt;br /&gt;
{{SubstanceInteraction|Chlorpromazine + Psychedelics|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:neutral.png]]|Chlorpromazine substantially diminishes the effects of DMT, LSD and other similar molecules (see Moore et al 1975, Shah &amp;amp; Hedden 1978}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=29012 'Known drug-interactions' Wiki page]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Harm reduction]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Known_substance-interactions_and_their_effects</id>
		<title>Known substance-interactions and their effects</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Known_substance-interactions_and_their_effects"/>
				<updated>2013-11-24T01:42:35Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* DMT + Mushrooms (psilocybin) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{ShowInfo|[[Image:Error.png]]|'''WARNING:'''|'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
This article is about the interactions and effects of  mixing different entheogens, both with each other and with medicine. Some combinations have a good synergy while others can be a DEADLY combination! Taking any substance carries a high responsibility, please read the WARNING section with great care!&lt;br /&gt;
&lt;br /&gt;
== Warning! ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: orangered;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&amp;lt;br /&amp;gt;&lt;br /&gt;
&amp;lt;span style=&amp;quot;color: red;&amp;quot;&amp;gt;'''THIS THREAD IS STILL 'IN THE MAKING' AND CAN CONTAIN WRONG DATA! DO NOT USE THIS THREAD AS A DRUG-INTERACTION GUIDE YET!'''&amp;lt;/span&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Even though the interactions of certain substances are described here, it is extremely important to be safe at all times! This article is only to give information about interactions and their effects, '''this article is NOT meant for advice on taking any combination!'''&lt;br /&gt;
&lt;br /&gt;
Many interactions described here are ''subjective descriptions'', so what is shown here is only an ''indication'' on how certain combinations can affect you and how safe they are. Many times those effects are dependent on dose (of each substance), route of administration, timeline of administration, set and setting, your mood, your physical health, your mental health and many other factors. &lt;br /&gt;
&lt;br /&gt;
== Psychedelics ==&lt;br /&gt;
&lt;br /&gt;
=== DMT ===&lt;br /&gt;
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Some report dysphoria at lower doses. I (House) do not find this to be the case I find low doses incredibly euphoric. Higher doses can be known to go beyond human emotions and concepts. Higher doses of DMT are also known to cause strange bodily hallucinations like the feeling that you have stopped breathing, or that your heart has stopped beating. These hallucinations are common and can be countered with conscious relaxation and meditation prior and during the experience. You do not have to submit, per se, but beware that you may have to let go of certain intensities during the experience. It can easily be the most &amp;quot;intense&amp;quot; experience of your life for some people, and this is *NOT* a bad thing!&lt;br /&gt;
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==== DMT + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Harmalas (MAOI)|#406040|#60FF60|OK|[[Harmalas]] potentiate and prolong the effects of [[DMT]], while at the same time it adds a slight psychedelic effect of it's own. For DMT to be orally active, a [[MAOI]] is mandatory.|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Oral activation. Potentiation. Slowed-down effect. The two go hand in hand creating a perfect synergy.}}&lt;br /&gt;
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==== DMT + Mushrooms (psilocybin) ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Mushrooms (psilocybin)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Another profound synergy that seems to unlock the potential of the [[mushroom]]. Either @ peak or after.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Positive.png]]|When DMT is smoked at the peak or post-peak of mushrooms, there is an extreme synergy that can make it for an incredible experience that can take one very very far! My favourite combo}}&lt;br /&gt;
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{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized DMT whilst on mushrooms- Potentiation, intense synergy between the two tryptamines, very strong visuals came thick and fast.}}&lt;br /&gt;
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==== DMT + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Negative.png]]|I didnt like it at all because it felt like LSD acts as an anchor and holds one down, preventing breakthrough}}&lt;br /&gt;
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==== DMT + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Euphoric, not as deep of a trip, but there is zero anxiety present which can be useful and awesome in it's own right.}}&lt;br /&gt;
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==== DMT + Mescaline ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Mescaline|#406040|#60FF60|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy here. Potentiates the [[mescaline]] and smooths it out.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Neutral.png]]|The mescaline seems to 'dull' the [[DMT]]. So there was not as much effects from smoking the DMT on Mescaline as you would expect.}}&lt;br /&gt;
{{UserDescription|Endlessness|[[Image:Negative.png]]|The mescaline seemed to hold the [[DMT]] towards the center of the vision, as if it didnt let it &amp;quot;expand&amp;quot;. I saw the DMT visuals curling up, like as if a magnetic/gravitational force didnt let it happen freely. The trip felt weird, it didnt feel 'natural' or 'flowing' to me. Tried it twice in different occasions to similar results and didnt feel like it's a good combination for me}}&lt;br /&gt;
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==== DMT + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Alcohol|#805000|#E0A040|SAFE But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|I find that combining the spice with a carcinogenic neurotoxin like [[alcohol]] completely negates the experience and masks it with toxic nullification (Yes, I am quite biased)}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The alcohol did  have a negative impact on me. I tried to drink a few beers beforehand to mitigate the anxiety of the [[pharmahuasca]] but that only resulted in dulling down, confusion and nausea.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|The Spice doesn't like Alcohol, you'll either wont remember or get a bad vibe.}}&lt;br /&gt;
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==== DMT + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK, although some people don't like it. If you are a daily cannabis smoker it shouldn't be a problem, but if you get anxiety from using [[Cannabis]] occasionally it may be wise not to mix it with [[DMT]].}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:neutral.png]]|If I smoke DMT / Changa 1-2 hrs after my last hit of cannabis it is great, if I smoke DMT &amp;amp; Cannabis together it is not so great.}}&lt;br /&gt;
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==== DMT + Dissociatives ====&lt;br /&gt;
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{{SubstanceInteraction|DMT + Dissociatves|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|By far my absolute favourite combination. This experience is equal in intensity as DMT but without the ego loss. An entirely new realm all together where YOUR controller. This can mean many things, its sheer awesomeness with seemingly no downside gives it quite an addictive quality. During my first encounters with this combination I probably went through more DMT in one night then I normally would have in months, maybe a year.}}&lt;br /&gt;
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=== Harmalas (MAOI) ===&lt;br /&gt;
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Side effects include contraindication with certain substances. Make sure you understand interactions with substances before using them! At higher doses users experience nausea and vomiting, but this also isn't necessarily a bad thing, since harmalas are anti-parasitic, purging is often considered cleansing to both the body and the mind. Chest pressure is also common with ayahuasca. Feelings of having something heavy sitting on you. This is normal and if experienced just relax and let it be, it's part of the serpents coil.&lt;br /&gt;
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==== Harmalas (MAOI) + Caffeine ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + caffeine|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally don't mind a low dose of harmalas on top of caffeine, it can counter act the sedation from the harmalas in the right dosages. Too much of both and you will experience uncomfortable heart rate. So new users to this synergy take caution and start low!}}&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|I had one cup of average strength coffee about 2 hours after smoking changa and I got very edgy and nervous. Coffee barely even wakes me up but I was wired for about an hour. Quite uncomfortable.}}&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|For me, a cup of yerba matè plus ayahuasca equals awful experience. There seem to be some people who can't take caffeine and ayahuasca}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + 5-MeO-DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + 5-MeO-DMT|#805000|#E0A040|OK But...|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|this could be hard on some metabolism, or dangerous, but IME, a great form of pharmahuasca, more nausea than with N,N-DMT, but also more euphorie.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Neutral.png]]|Harmalas will significantly increase potency of 5-MeO-DMT. 40-60mg harmaline + 10mg 5-MeO-DMT orally is equivalent to 30-35mg oral 5-MeO-DMT by itself or 10 mg intranasally (see Ott 2001 Note that 35mg by itself was not active dosage to shulgin but was for ott}}&lt;br /&gt;
{{UserDescription|Picatris|[[Image:Negative.png]]|Potentially unsafe combination and health risks due to metabolic issues. For more info search the forum for the thread titled &amp;quot;Does Anyone Here Eat 5-MEO-DMT?&amp;quot;.}}&lt;br /&gt;
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==== Harmalas (MAOI) + Kava kava ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + Kava Kava|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
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==== Oral Harmalas (MAOI) + Opioids ====&lt;br /&gt;
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{{SubstanceInteraction|Oral Harmalas (MAOI) + Opioids|#604040|#FF6060|BAD IDEA!|Has the potential for adverse reactions, namely CNS excitation or depression (resulting in high or low blood pressure).|&lt;br /&gt;
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==== Oral Harmalas (MAOI) + L-dopa ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + L-dopa|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|taking levodopa with MAOIs runs the risk of a hypertensive crisis and levodopa should not be taken for at least 2 weeks after MAOIs; the risk of taking RIMAs (specifically moclobemide) with levodopa is one of increased side effects which include anorexia, nausea, vomiting, agitation, postural hypotension, tachycardia, arrythmias, hypomania, psychosis, depression, headache, flushing, gastrointestinal bleeding, itching, rashes, abnormal involuntary movements. &lt;br /&gt;
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The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinations}}&lt;br /&gt;
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==== Oral Harmalas (MAOI) + tyrosine ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas + tyrosine|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Corpus Callosm|[[Image:Negative.png]]|l-tyrosine taken with MAOIs renders it more likely to be a vasopressor ie cause an elevation in BP.&lt;br /&gt;
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The thing to recognise about such advice is that some people may not suffer such adverse effects, but there is a significant likelihood of having such a response that it can only be considered wise to avoid such combinationss}}&lt;br /&gt;
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==== Harmalas (MAOI) + Dissociatives ====&lt;br /&gt;
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{{SubstanceInteraction|Harmalas (MAOI) + Dissociatives|#604040|#FF6060|BAD IDEA!|Even though there are reports on the net of people combining MXE with harmalas, in the right dosages harmalas + dissociatives have the potential to cause cardiac arrest.|}}&lt;br /&gt;
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=== Mushrooms (psilocybin) ===&lt;br /&gt;
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I (House) think the most common side effect I hear about with shrooms is stomach discomfort. A lot of people don't know that you really are not supposed to consume any kind of raw mushroom. It's a rare case in the culinary and medicinal fields where raw mushrooms are told to be ingested. (I can think of a few exceptions, of course.) So for some ingesting the raw material can be very nauseating, myself included. Making a tea or the lemon tek is the way to go. By soaking raw mushrooms in lime juice, the citric acid literally cooks the mushrooms breaking down the cell walls. This is also known as a ceviche in the cooking world. Personally I just slip the shot of lime juice with the mushrooms in it back, it tastes good and I don't experience nausea this way. Some people filter out the mushroom material from the solution. Experiment. Taking too many mushrooms can lead to a feeling of being poisoned, but as far as I know no one has ever died from taking them on their own. Dose accordingly!&lt;br /&gt;
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==== Mushrooms + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I won't use mushrooms without cannabis; Noticeable synergy and eases any anxiety present. Some people who don't use cannabis often find that this combo causes paranoia.}}&lt;br /&gt;
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==== Mushrooms + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Profound synergy. Great for meditation and dance}}&lt;br /&gt;
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==== Mushrooms + Harmalas (MAOI)====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Harmala (MAOI)|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love the harmala + mushrooms synergy, but some have noted that the harmalas potentiate the mushrooms very much and have had rough trips! If you want to experiment with this combo, start low and work your way up!}}&lt;br /&gt;
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{{UserDescription|Mindlusion|[[Image:Neutral.png]]|I tried this combo at a fairly high dose, it GREATLY potentiated the effects.. And I absolutely loved it, quite more then the intensity I was looking for. Although after the first 6 hours, I felt the trip had come to conclusion, I was ecstatic, but physically and mentally exhausted, only to have the experience continue at practiaclly the same intensity for ANOTHER 6 hours. Before I could get any sleep whatsoever.  If you try this combo, its great, just be prepared to trip for a LONG time.}}&lt;br /&gt;
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==== Mushrooms + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Alcohol|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, slower than cocaine however. Also, people tend to get negative from this combo. One might hypothesize that alcohol tends to turn the trip in a darker direction.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad idea, high chances to end up puking and feeling miserable.}}&lt;br /&gt;
{{UserDescription|Frankycou|[[Image:Negative.png]]|This is potentially very unsafe! some type of mushroom are known to develop poison when mixed with alcohol. This is very rough information that I am reporting since I don't remember the exact text and source but basically I read from a reputed source that some types are EXTREMLY BAD  to mix and should be avoided at all cost.}}&lt;br /&gt;
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==== Mushrooms + Alcohol + Cocaine + MDMA====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Alcohol + Cocaine + MDMA|#604040|#FF6060|BAD IDEA!|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Negative.png]]|Bad bad idea. I took the MDMA, Coke and Alcohol at the end of a Shrooms trip. Anxiety and profound guilt were felt in my whole body}}&lt;br /&gt;
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==== Mushrooms + Cocaine ====&lt;br /&gt;
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{{SubstanceInteraction|Mushrooms + Cocaine|#805000|#E0A040|SAFE But|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:Negative.png]]|Tends to dull the trip, or even stop it dead in it's tracks.}}&lt;br /&gt;
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=== LSD ===&lt;br /&gt;
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LSD is a potent vasoconstricting substance. This means it causes an increase in blood pressure by tightening the blood vessels in the body. This can be countered with vasodilating substances. Some find that oral hash completely diminishes the vasoconstriction. I like using transdermal magnesium prior to a dose to also help with things like jaw tension. Also, conscious relaxation, deep breaths, and massage (even done by the self) can help curb tension experienced from the drug. If you feel over stimulated or uncomfortable, you probably need to &amp;quot;Flow&amp;quot;, so to speak. Get up, stretch, dance around, laugh, have an orgasm, be creative, play a musical instrument, take a hot shower. Things like this help with getting energy flowing and making meditation easier. Eat a bit of fruit on the come-up if you feel some unease! Many people find cannabis greatly eases the transition, but of course not everybody. &lt;br /&gt;
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==== LSD + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Profound synergy. Really adds another more controlled layer to the hyperspatial flow. Highly recommended @ the peak or after the peak.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|Euphoric, less anxiety. NOTE: For me it's best to take the [[DMT]] on the trail of the [[LSD]] and not on the peak of the LSD.}}&lt;br /&gt;
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==== LSD + Ayahuasca + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Ayahuasca +DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is my favorite synergy of all time. First take the LSD, then take a comfortable dose of banisteriopsis caapi tea, then smoke as much DMT/Changa as you desire. Absolutely astonishing.}}&lt;br /&gt;
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==== LSD + Mushrooms ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mushrooms|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A lot of people don't like this combination for some reason- both drugs are just so powerful they may not need to go together, with that said however some people like the combo and it is OK to take.}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy with Psilocybe mushrooms.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|I took the Mushrooms while coming down from the LSD and I didn't feel any effect whatsoever. (EDIT: You probably have to take lots of Shrooms to fight the tollerance)}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I haven't experimented enough with this combination to say for sure. Only very small doses, and they were kind of hazy.}}&lt;br /&gt;
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==== LSD + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Classic Combo. Take at the same time or let the acid kick in then take the MDMA. Profound synergy!}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDMA gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|MDMA and LSD together is one of the most amazing synergy in terms of dancefloor experience...}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|The only time I did it, I took the LSD a while after the MDMA. Everything was very smooth and shiny. Great dancing combo!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|&lt;br /&gt;
MDMA removes any negative experiences I feel with LSD. POWERFULLY beautiful combination! All aesthetics are increased 10x, music is beautiful and flowing, playing music is amazing, dancing is amazing. Cuddling, hugging, telling people you love them... yes, this is a winner.}}&lt;br /&gt;
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==== LSD + MDAI ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MDAI|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Positive.png]]|The MDAI gives a euphoric effect to the LSD experience.}}&lt;br /&gt;
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==== LSD + Mescaline ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy but it's hard to tell how each drug is affecting each other. A bit like LSD + MDMA but a deeper, so to speak.}}&lt;br /&gt;
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==== LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Cannabis vasodilates the vasoconstriction of LSD especially if taken orally. Potentiates and smooths out the trip. Great for daily smokers. Has been known to cause anxiety in those who don't use Cannabis too often.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|I almost never use [[cannabis]], I wanted to use the cannabis versus the stimulation of the LSD. It gave me more visuals but it also made me dizzy. Overall I did not like it.}}&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|Definitely has led to a bunch of paranoia at times (I'm prone to that with weed alone though) but if combined carefully it can be totally worth it although i never do it anymore (no lsd). If a large amount is smoked at the peak-especially if i have a low tolerance- then it can really catapult the experience into a sort of out of body type thing with full blown 3-d immerse visions, IME}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:neutral.png]]|It gives a bit of anxiety, although the effect of LSD is potentiated for a little while. Be aware, it's very hard to roll a spliff while tripping }}&lt;br /&gt;
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==== LSD + Cannabis + Tobacco====&lt;br /&gt;
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{{SubstanceInteraction|LSD + Cannabis + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I mostly smoke spliffs, but I find spliffs (a 50/50 mix of cannabis and tobacco) To be quite pleasant at all periods of the LSD comeup. Usually my physical form is quite shakey and or cold during the LSD comeup, and cannabis warms me up and calms down any tension or shakiness. Spliffs induce a deep trance state for me, very pleasant.}}&lt;br /&gt;
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==== LSD + MXE ====&lt;br /&gt;
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{{SubstanceInteraction|LSD + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Aetherius Rimor|[[Image:Negative.png]]|Did 30mg of [[MXE]] in the 2nd hour of 2 hits. That's the only time I've not been at home and unable to verbalize/coordinate movement. Luckily that's what designated drivers are for! Won't combine them again. Definitely stronger effects than same dose of each independent of each other.}}&lt;br /&gt;
{{UserDescription|The Traveler|[[Image:Negative.png]]|The MXE potentiates the [[LSD]] effects with more visuals but it also significantly alters motor function to the point of immobility at high doses.}}&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Radical and profound potentiation/synergy. 12+ hour trip and much longer to sleep. I really love the synergy of LSD+MXE but I'm the kind of person who naturally chills during a trip, so being pancaked by effects is just an extra plus for me.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|I have tried this combination many times, but only at high doses of MXE, I loved this combination, it intensified and increased the depth and power of the dissociated 'hole' while making it easier to bring back more from the experience. The only negative effects Ive felt is the dissociated 'whobblies' that last for an hour or two after the hole, which can be annoying while trying walk around on LSD. In my experience, it is best taken early in the LSD trip, when the effects subside you are usually at the LSD peak, this also seems to ease any anxiety. (I would also like to mention I am quite mobile at high doses of MXE while on LSD, only after mobility can be hindered by the drunken like 'whobblies')}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Amphetamines ====&lt;br /&gt;
{{SubstanceInteraction|LSD + Amphetamines|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:neutral.png]]|Somewhat safe but...Makes the LSD less visual and a bit more difficult to handle mentally because of the stress caused by the stimulants. It can be an interesting mix if partying but I would try to avoid it if possible. At least try to get pharmaceutical grade stimulants and not dirty street pills.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Harmalas (MAOI)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|You MUST make sure you have pure LSD, however! You do not want to mix harmala (RIMA, MAOI) with an unknown drug laid on blotter. It's great taken with a dose or taken after the dose has kicked in, as the vasodilation of the harmala counters the vasoconstriction of the LSD.}}&lt;br /&gt;
{{UserDescription|Enoon|[[Image:Neutral.png]]|Super strong synergy, stronger than usual visuals, visions, OBE, but also nausea, imobility and substatial amount of apprehension}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Strong synergy/potentiation, first timers should take very small doses to see how they react and only raise gradually.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I must admit I'm a bit of a Harmala &amp;quot;fiend&amp;quot;. I love them and I see no negative applications to them, pretty much, as long as you are physically safe. They potentiate the visuals of LSD, get rid of the shakes and nervousness, help me emotionally sort through things and make me warm and content and happy. This is a WINNING combination, especially with chocolate caffeine or spliffs. all very good in my books. Great for meditation, dancing, writing, drawing, or playing music.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Amanita Muscaria/Pantherina ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Amanita Muscaria/Pantherina|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Great synergy, tends to make the trip more challenging and more visionnary, more entheogenic also, but it is again harder than LSD on it's own.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + Alcohol====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Mescaline|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|Doesn't make sense to me to combine a CNS depressant with the brilliant effects of LSD.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Great and jolly, but it makes the trip a bit blurry and less powerful. Don't over do it, your liver wont appreciate it!.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't enjoy alcohol in general, so I'm slightly bias. When I was younger (15-16) I would shotgun beers on LSD and that was quite nice, but any hard alcohol combined with LSD turns you into a flailing, falling idiot apologizing for making such a big mess.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== LSD + GHB====&lt;br /&gt;
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{{SubstanceInteraction|LSD + GHB|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:neutral.png]]|I don't have enough concrete experience with this combination, but I haven't experienced negative interactions the few times I have done them. the GHB is very warm and mellow, although a bit of nausea or headache or spinny-ness can occur at higher doses, if everything is kept moderate it is much more pleasant than alcohol, although not quite as pleasant as MDMA.}}&lt;br /&gt;
}}&lt;br /&gt;
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=== Mescaline ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Mescaline is a phenethylamine that does not have an amphetamine group on the molecule, unlike MDMA. This allows it to be able to be used with harmalas without contraindication. A very gentle and long lasting psychedelic with great empathic and stimulating properties. &lt;br /&gt;
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==== Mescaline + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mescaline + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|A great way to potentiate your mescaline dose is with caffeine, especially coffee. Yerba mate and other teas are good too. Even the days after a trip, a nice cup gets you right back in that lovely state-of-mind. Some may find this combo too stimulating, however. The coffee can also be used to get digestion flowing if you are having indigestion from the cactus.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Noticeable potentiation and takes the edge off the stimulation subsequently. These two go hand-in-hand if you are a regular cannabis user. If not, start low!}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Harmala|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|No contraindication here. A nice synergy. The harmala takes away some of the stimulation of the mescaline and makes the experience more dreamy. }}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + Alcohol ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:negative.png]]|You can drink a lot of alcohol on mescaline, but I don't see the point. Takes away from the profound effects of the psychedelic.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|In high doses it's extremely confusing! Good chances to blackout and puke. }}&lt;br /&gt;
}}&lt;br /&gt;
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==== Mescaline + MDMA ====&lt;br /&gt;
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{{SubstanceInteraction|Mescaline + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Nice combo, but it wasn't enough to understand its effects.}}&lt;br /&gt;
}}&lt;br /&gt;
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=== Iboga ===&lt;br /&gt;
&lt;br /&gt;
Careful with this one! Much research and tests must be done before ingesting this substance. It is clinically proven to slow down a rhythm of the heart beat and has killed people because of this. A heart panel and EKG are common tests preformed before ingesting this substance. Please beware of this and do a lot of research before even considering this very profound medicine! Side effects include disorientation, immobility, nausea, in high doses for very long periods of time. Some people still can't drive a car 1 week after a flood dose, for example.&lt;br /&gt;
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==== Iboga + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|LSD becomes much more potent after Iboga and I would suggest taking it sometime between 1-7 days after taking a low dose of Iboga. For me I find that the LSD really puts the teachings of the Iboga into perspective. Be careful though, there is a definite potentiation.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:negative.png]]|very challenging in my experience so the LSD was probably very high (vial wash) with loads of noribogaine (2 grams RB every days for four to five days) in the system. I personnally wouldn't recommend it.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Mushrooms ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I find that psilocybe mushrooms are a really great synergy. They seem to kick in the Iboga about 3x as hard, so a low dose of both makes for a good journey. Euphoric, meditative, deep combination. Great for sorting things out in your life.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with Iboga and cannabis. Noticeable potentiation. Also takes care of the intense nausea with higher doses of Iboga a bit. I believe this synergy is even used traditionally in some instances.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:Positive.png]]|Iboga and canabis are great together, the iboga focus the train of thought from canabis while canabis relax the iboga (stimulant at low doses) experience.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Harmala|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|While myself and others have found a low dose of harmala to be a nice synergy with Iboga, others have found the combination too intense. Start low and work your way up.}}&lt;br /&gt;
{{UserDescription|rOm|[[Image:positive.png]]|Iboga and harmalas must be treaten with caution though in low doses, it seems like a very good combo though questionnably safe (in regards of mixing RIMA and SSRI).}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Iboga + Coffee ====&lt;br /&gt;
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{{SubstanceInteraction|Iboga + Coffee|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I personally love a low dose of Iboga with a good cup of coffee, and cannabis. I find it stimulating both physically and with the clarity of mind. Some may find this too stimulating. Don't expect to sleep the night of taking this combo!}}&lt;br /&gt;
}}&lt;br /&gt;
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=== MDMA ===&lt;br /&gt;
&lt;br /&gt;
The most common side effects of MDMA are jaw tension, feeling burnt-out the next day, and it's minimal amount of neurotoxicity.&lt;br /&gt;
A lot of people &amp;quot;pre load&amp;quot; with substances that are neuroprotectant before, during, and after the experience. Neuroprotectants include cannabis, nootropics, vitamin C, 5-HTP, and others. Jaw tension can be countered again with transdermal magnesium, conscious relaxation, meditation and massage. As for feeling burnt-out, try to only redose a small amount one time or not at all. Constantly redosing can cause more burnout srensations. Also dosing too high. You might want to touch, hug, kiss, and tell how much you love everything around you, too.&lt;br /&gt;
  &lt;br /&gt;
Taking MDMA with MAOI and certain prescription medications can lead to seratonin syndrome and even death so plesse be careful!&lt;br /&gt;
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==== MDMA + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + Harmalas (MAOI)|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Great synergy with MDMA and cannabis. Smooths out the stimulation. Biologically speaking, the cannabis actually works as a neuroprotectant against the neurotoxicity of MDMA. They go hand-in-hand if you are a fan of cannabis!}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Very nice, but you end up smoking way too much.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + LSD + Ketamine + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + LSD + Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Better than OK for me. Have had some of the best nights of my life with this cocktail.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== MDMA + DMT + Ketamine ====&lt;br /&gt;
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{{SubstanceInteraction|MDMA + DMT + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Out-of-this-world OEVisuals. The euphoria of the MDMA is present and the visual quality of the K synergizes with the DMT in a very strange way. I would suggest taking only small dosages with all of those three if you are to give this combo a try.}}&lt;br /&gt;
}}&lt;br /&gt;
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=== Ketamine ===&lt;br /&gt;
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==== Ketamine + LSD ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|This is a pretty classic and noteable synergy that many people love. The K takes you very deep into yourself, and away from yourself at the same time.}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. Similar to the 2CB combo, be careful, both of these drugs have a tendency to be a bit mind bending, and in combo, expect it to get wild!}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|LSD + Ketamine is definitely a strange combination. In my experience it lends itself to meditation because alot of the time the mind is too befuddled to properly draw a train of thought. I find this combination quite inarticulating, it's one of the few drug interactions that make me a bit of a &amp;quot;dumbass&amp;quot;, and just puddle me on the floor. Lower doses of ketamine + lsd are good for dancing, higher doses, for trancing.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + LSD + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + LSD + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Love it!}}&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. You will get lost in the deepest recesses of your mind for quite some time, I love comatose tripping, but it isn't for everyone.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + Harmalas (MAOI) ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Harmala|#604040|#FF6060|BAD IDEA!|Harmalas are contraindicated with dissociatives, this means you do not want to combine them. At high doses the cardiovascular system can shut down.|&lt;br /&gt;
{{UserDescription|House|[[Image:Negative.png]]|Made the mistake of trying changa on top of LSD + K once and I will never do that again. Intense bronchial constriction and chest pain was noted.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coming back from the ketamine trance and smoking cannabis. Great for meditation and integration if you enjoy cannabis!}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + DMT ====&lt;br /&gt;
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{{SubstanceInteraction|Ketamine + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|DMT on Ketamine is out of this world stellar. The dissociative properties of ketamine completely eliminate any anxiety present, and the two work together to take you deep into whatever it is that we are...}}&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Some people suggest ketamine may smooth the entry int tryptamine space and some report incredible experiences. Special care is needed with ketamine due to it's potentially addictive nature and due to being dissociative/anaesthetic and increased risks of physical accidents. Justin Case's best results have been reported when k dose is kept low and tryptamine dose is solid but not excessive.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|This combination is grandeur, extremely powerful. I agree with both House and Endlessness, especially about the addictive part. Extensive use of the this combination and other DMT + Dissociatives, seems to make a preexisting addiction worse. It's a lot of strain on ones psyche to abuse this combo.) }} &lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + LSD + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + LSD + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Throwing DMT into the mix is just that much more powerful.}}&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|^ What House said.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Some people love it, I don't. I don't like small bumps of K, so when I take it, it always end up taking over all the rest.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Ketamine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Ketamine + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|I heard it's not very safe. I did it few times and the day after I always felt miserable.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
===Salvia Divinorum===&lt;br /&gt;
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==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|OK. can be extremely disturbing though or unbelievably profound and real.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Salvia + Changa + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Salvia + Changa + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is probably my favorite mix. I've had some of my deepest experiences mixing these three including one with multiple breakthroughs one on top of the other cascading deeper with a new universe created and destroyed each time.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Salvia + Cannabis ====&lt;br /&gt;
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{{SubstanceInteraction|Salvia + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mysmelf|[[Image:Positive.png]]|This is a very therapeutic anesthetic. This kills pain very well and leaves me in a dreamy visionary state without the mind warping dissociating effects that salvia has on its own. As long as you don't go heavy on the salvia! }}&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good! Great way to take the edge off of the pre-flight anxiety for salvia, which can be pretty rough at times.}}&lt;br /&gt;
}}&lt;br /&gt;
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==== Salvia + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Effects are dramatic but its not clear if there is synergy or more like additive effects. }}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
== RC's ==&lt;br /&gt;
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&lt;br /&gt;
=== 2C-B ===&lt;br /&gt;
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==== 2C-B + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-B + Ketamine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Have seen 2 people lose the plot on this combo, so be careful. For me, it subdues the edginess of the phenethylamine buzz, while adding a trippy colourful edge to the Ketamine. Can get confusing, which I think was why people freaked out a bit.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== MDMA + 2CB + K + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + 2CB + K + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|Similar to the above, moar euphoria, but again please be careful with dosages.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== 2C-I ===&lt;br /&gt;
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==== 2C-I + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|2C-I + Cannabis|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:negative.png]]|made me feel sick, smoking anything on 2CI wasn't nice.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
=== MXE ===&lt;br /&gt;
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==== MXE + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MXE + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Purges|[[Image:Positive.png]]|OK. deep, visual, introspective, make sure you don't have anything to do / people to entertain as chances are you will be lost in thought. Did experience a little muscle tremoring, but less than 2CI on its own.}}&lt;br /&gt;
}}&lt;br /&gt;
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&lt;br /&gt;
==== 5-MeO-DALT + MXE ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|5-MeO-DALT + MXE|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|gory dkalz|[[Image:negative.png]]|While on ~50mg 5-MeO-DALT orally I did a little test bump of 15 mg MXE insufflated and within minutes felt my heart rate go up and felt very dizzy. Thought that I had finally done it and mixed the wrong stuff and I would have to go to the ER but it stopped escalating and I just waited it out.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== 25i-NBOMe ===&lt;br /&gt;
&lt;br /&gt;
==== 25i-NBOMe + Cannabis + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|25i-NBOMe + Cannabis + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|billydgator|[[Image:Positive.png]]|Awesome! About 2.5 hours into an 25i nbome trip i took some small blasts of spice, brought me from ++ to ++++.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== AM-2201 ===&lt;br /&gt;
&lt;br /&gt;
==== AM-2201 + MDMA ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|AM-2201 + MDMA|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Nice high, feels good and very sedating, very happy and relaxed. But can be VERY hallucinogenic, only smoke a little! Bizarre and realistic and gory hallucinations (man with half a leg bleeding allover the place!) are possible, voices become distorted and merged and speak impossible ridiculous things. The hallucination is short lived.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== MDAI ===&lt;br /&gt;
&lt;br /&gt;
==== MDAI + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDAI + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Orion|[[Image:Positive.png]]|Vaporized hits of DMT seem harder to break through on, but the effect of the DMT seem prolonged. Strange visuals (small pinpoint kaleidoscope patters appear and dissappear), last for longer than the spice effects would last, by up to 25 minutes longer. Does not seem dangerous, but the fact it makes open eye visuals linger for so long is interesting...}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Medicine ==&lt;br /&gt;
&lt;br /&gt;
=== SSRI/SSRE ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Harmalas (MAOI) + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + SSRI/SSRE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Harmalas (MAOI) + SSRI/SSRE|#604040|#FF6060|BAD IDEA!|Hypertension, Serotonin Syndrome. '''Death''' can result out of this combination!|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Cannabis ===&lt;br /&gt;
&lt;br /&gt;
Cannabis works as a potent anti-inflammatory and vasodilating medication. Those who use it often find that it goes well with almost every other drug, while those who seldom use it may find that when combined with psychedelic substances it can cause paranoia and uncomfortable potentiation. If you are unfamiliar with the ways cannabis synergizes with other substances, it is wise to start low and work your way up to a comfortable amount. Many find that oral cannabinoids act as a more potent vasodilator than smoked, making this a good option for countering the vasoconstriction of drugs like LSD and LSA. Many people also use cannabis to counter the nausea caused by other drugs. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Cannabis + Harmalas (MAOI) ====&lt;br /&gt;
{{SubstanceInteraction|Cannabis + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:positive.png]]|Harmalas potentiate the effects of cannabis, adding a nice dreamy feel and tracers to the vision. Since they are both vasodilating compounds, some people experience headaches if combined in high doses. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Other ==&lt;br /&gt;
&lt;br /&gt;
=== Nootropics/Piracetam/Aniracetam ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Piracetam + Psychedelics/Amphetamines ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Piracetam + Psychedelics/Amphetamines|#805000|#E0A040|OK but|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|Trout notes that justin case, toad and others have reported substantial increase in potency of phenetylamines (such as MDMA, mescaline, amphetamines) and suggest dosage is halved. Possible potentiation of tryptamines too. There is very little data on the pharmacodynamics and toxicity of this mixture, so care is adviced, even though due to low toxicity of tryptamines and piracetam by itself, its possible the toxicity of mixture is also low.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== LSD + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I have been dosing piracetam daily for a few weeks now, and in that time I've done LSD twice. Definitely noticed that each time the piracetam VASTLY improves ability to articulate myself, ability to recall the trip and get into deeper meditative states. Piracetam also greatly helps my ability to write more clearly in my journals, improves my ability to play music and LSD enhances my musical creativity. All in all, very good combination.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Caffeine + Piracetam ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Caffeine + Piracetam|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dream Weaver|[[Image:Positive.png]]|I occasionally dose piracetam anywhere from 800mg to 4 grams ingested on an empty stomach (dissolved in water). I find the synergy of caffeine + piracetam to be quite soothing. It is important not to ingest too much caffeine or an anxiety like feeling will occur/stomach problems... Mostly positive if done right. Effects are very soothing and uplifting. Make the most mundane task entertaining. You become quick and sharp as a whip. Somewhat similar to 30mg xr adderall + 5-15mg valium. Great combo! Ideal for mornings!}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Kava Kava ===&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + DMT ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava kava is relaxing and aids in dissipating pre-flight anxiety. A warm cup is great after DMT insufflation or vaporization. There is a noticeable synergy between the two and no discomfort or side effects have been noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + LSD ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Kava Kava after the peak of LSD when it's wearing off is a great way to take the edge off and get some rest. It's very effective and enjoyable this way with no side effects noted.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kava Kava + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kava Kava + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Nice synergy. Very relaxing.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== DXM ===&lt;br /&gt;
&lt;br /&gt;
==== DXM + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|Great. Visually incredible. Cannabis at peak enhanced visuals even further. Use more mushrooms than DXM.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== DXM + Cannabis ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Cannabis|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Good. Great way to up the psychedelic aspect of dex.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Tobacco ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Tobacco|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Great. Dex really makes tobacco shine, brings out the best world of nicotiana.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + NO2 ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + NO2|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|Very, Very intense. Too much for some people, but for others, euphoria.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + HBWR (LSA) ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + HBWR(LSA)|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Positive.png]]|It really increases the psychedelia of dex, brings some awesomely colorful visions, but be very careful. Not much is known about the interactions of these two. I would not go above 3 HBWR seeds in combo.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + DMT ====&lt;br /&gt;
{{SubstanceInteraction|DXM + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Mindlusion|[[Image:Positive.png]]|One of the most intense experiences I could possibly imagine. Classic Dissociative + DMT, but incomparable at the same time, I could say I like this combination better then DMT + Ketamine, or DMT + MXE, but its incomparable.  It dissolves any preflight, or during anxiety whatsoever, the utterly intense godly power of DMT is given to YOU. }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Chocolate/Theobromine ===&lt;br /&gt;
&lt;br /&gt;
Theobromine, a methylated xanthine found in chocolate and yerba mate, is a stimulant and psychedelic potentiator.&lt;br /&gt;
&lt;br /&gt;
Low doses combined with psychedelics causes noticeable potentiation and empathy.&lt;br /&gt;
High doses have the potential to cause nausea and over stimulation, so start low and work up to a comfortable dose!&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|Aka The Mocha. Nice warm fuzzy sociable synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Caffeine + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Caffeine + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Definite potentiation and synergy.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Passionflower ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Passion Flower|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:neutral.png]]|OK, but don't use a lot of theobromine. I have had psychedelic effects with this combination, but also intense nausea and bronchial-constriction at higher doses.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Harmalas (MAOI) ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Harmalas (MAOI)|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK but do not use a lot of theobromine or harmala. A little goes a long way! Same thing goes here if you have a little too much of either theobromine or harmala expect nausea and vomiting. At appropriate doses however the synergy is very nice. Theobromine potentiates the harmalas and any psychedelics you take as well.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I haven't experimented too heavily with eating cacao on LSD, but I usually eat one or two handfulls of raw cacao nibs. I found the stimulation synergistic, very good for walking or running through the forest. I found that the cacao gets rid of the &amp;quot;shivers&amp;quot; I experience from LSD and warms me from the inside.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Theobromine + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Theobromine + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|OK. Noticeable synergy and potentiation}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Kratom ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Kratom + MXE ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Kratom + MXE|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Pandora|[[Image:Positive.png]]|Effects: Like 10-15 mgs of Hydrocodone.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== NO2 ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Mescaline ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Mescaline|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Jabbawaya|[[Image:Positive.png]]|NO2 at peak of a mescaline trip was incredibly euphoric. Felt like psychedelic MDMA.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + DMT ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + DMT|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:Positive.png]]|When nitrous is inhaled immediately after dmt, its reported by some people to significantly enhance the experience.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + LSD ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + LSD|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|OK. Very powerful. Be prepared to lie down and be somewhat paralyzed, depending on dosage.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Ketamine ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Ketamine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|ChaoticMethod|[[Image:Positive.png]]|Amazing visuals. Out of body experience, very comfortable but no contact at all with the body.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== NO2 + Mushrooms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|NO2 + Mushrooms|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:Positive.png]]|Amazing! For few minutes you are in a DMT like world. (I'd love to try LSD + NO2)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
=== Alcohol (Ethanol) ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== DXM + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|DXM + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:neutral.png]]|I have done this a few times and been safe, but I was very careful and spaced my drinks out. I have read horror reports of people drinking to much on dex, and puking for upwards of an hour or two.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Salvia + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Salvia + Alcohol|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|tigerstrike92|[[Image:Negative.png]]|Puke city.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== MDMA + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|MDMA + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Bedazzle|[[Image:negative.png]]|Another potential Show Stopper. The Alcohol really tends to lessen, dull, or end the effects of the mdma. Aside from that, there is the danger of dehydration--when you are rolling you should drink water.}}&lt;br /&gt;
{{UserDescription|Dante|[[Image:positive.png]]|Quite nice, but do not over do it! If you have been drinking too much, you'll be hit by a train when the MDMA comes down.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
==== Bufotenine + Alcohol ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Bufotenine + Alcohol|#805000|#E0A040|Safe but|...|&lt;br /&gt;
{{UserDescription|Dante|[[Image:negative.png]]|Not a good combo. The Bufotenin's nausea will probably make you puke and the Alcohol will diminish the Bufotenin visual effects.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Caffeine ===&lt;br /&gt;
&lt;br /&gt;
==== Mushrooms + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Mushrooms + Caffeine|#805000|#E0A040|Depends|...|&lt;br /&gt;
{{UserDescription|obliguhl|[[Image:negative.png]]|Not so good. Caffeine disturbs the mushroom flow.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== LSD + Caffeine ====&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|LSD + Caffeine|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|House|[[Image:Positive.png]]|I love coffee or yerba mate with LSD. Wonderful combo.}}&lt;br /&gt;
{{UserDescription|Shadowman-x|[[Image:Positive.png]]|I'm a bit of a coffee / mate junkie, so I find the combination quite synergistic. Smoking a spliff and drinking coffee on LSD makes me feel like all is right in the world and I can sit in meditation and take a good 30 minutes to drink my coffee and have my smoke. It lends itself to visual enhancement and incredible tingling sensations in the body, which for some people could make them quite restless, but I enjoy meditation on stimulants.}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Melatonin ===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Melatonin + Mushrooms + Harmala + Cannabis + Changa ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{SubstanceInteraction|Melatonin + Mushrooms + Harmala + Cannabis + Changa|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|Universecannon|[[Image:Positive.png]]|50-100mg melatonin (very meditative and harmala-esque for me. Combines well with others like a mind lube. A few hours later - lower dose of oral harmalas (preferably caapi) + mushrooms + smoked Cannabis + changa to top it off and push it all through. Amazing synergy. Need to balance the ratios accordingly though. You can leave out the melatonin if your not used to higher doses (they're not really that sleepy like the lower doses though, oddly). I prefer this combo after a day or to without sleep. Sleep deprivation is a powerful means of accessing altered states that's been used for thousands of years, like in the epic of Gilgamesh, for example. That's not for everyone though and works best with a raw, plant based diet.)}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Benzos/Barbituates ===&lt;br /&gt;
&lt;br /&gt;
Benzodiazepines can be reduce an agitated rough/unpleasant trip but are generally not recommended if other non-invasive supportive care-taking can be done, because these substances will dull the consciousness and might prevent the tripper from learning from the hard experience and integrating it.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Chlorpromazine + Psychedelics ====&lt;br /&gt;
{{SubstanceInteraction|Chlorpromazine + Psychedelics|#406040|#60FF60|OK|...|&lt;br /&gt;
{{UserDescription|endlessness|[[Image:neutral.png]]|Chlorpromazine substantially diminishes the effects of DMT, LSD and other similar molecules (see Moore et al 1975, Shah &amp;amp; Hedden 1978}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=29012 'Known drug-interactions' Wiki page]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Harm reduction]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:29:54Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
DMT Nexus user reports:&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with residual low effects over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=51413 Arcologist])&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:29:25Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
DMT Nexus user reports:&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with residual low effects over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=51413 Arcologist])&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:23:35Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with residual low effects over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=51413 Arcologist])&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:22:29Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with residual low effects over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=503394&amp;amp;#post503394 arcologist])&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:20:31Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with residual low effects over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. (https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=503394&amp;amp;#post503394)&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:19:51Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
* A higher body load and lower visual and mental activity than DMT. (https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=503394&amp;amp;#post503394)&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/NMT</id>
		<title>NMT</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/NMT"/>
				<updated>2013-11-23T03:19:24Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
[[Image:Nmt.jpg|thumb|right|300px|''NMT Molecule'']]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is NMT? ==&lt;br /&gt;
&lt;br /&gt;
NMT is a tryptamine found in several plants, previously thought to be inactive, but novel research done by [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Nen888] has shown it to be psychoactive.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
For solubility, melting point, etc, check the [[Psychedelic Compounds Chemical and Physical Properties#NMT|NMT Chemical and Physical Properties]] WIKI&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
* 1/3 to 1/4 potency of DMT. A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter. [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=269093#post269093 Nen (2001)])&lt;br /&gt;
&lt;br /&gt;
A higher body load and lower visual and mental activity than DMT. (https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=503394&amp;amp;#post503394)&lt;br /&gt;
&lt;br /&gt;
* Further info: [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml TIHKAL NMT entry]&lt;br /&gt;
[https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=23544 Entheogenic Effects of NMT]&lt;br /&gt;
&lt;br /&gt;
A slower onset than DMT, coming up after about 3-5 minutes and peaking within a minute, with a gradual taper over an hour to 70 minutes thereafter.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
*Present in trace amounts as part of normal metabolism ([http://www.ncbi.nlm.nih.gov/pubmed/11763413 Source])&lt;br /&gt;
&lt;br /&gt;
== Plants containing NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Acacia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Acacia albida]]&lt;br /&gt;
* Possible but unconfirmed presence. Detected· in Fall 1993, Spring, Summer, Fall 1994 and Spring 1995; tlc by Appleseed.&lt;br /&gt;
&lt;br /&gt;
[[Acacia confusa]] (=A. richei A .Gray)&lt;br /&gt;
* Unspecified amount in bark. Lou et al. 1965&lt;br /&gt;
* 1.43% in (dried?) root-bark Liu et at. 1977 (55.25% of total alkaloid) Root bark total alkaloid content was 2.58%&lt;br /&gt;
* 0.04% in dried stem Arthur et at. 1967 (8.8 kg. of stems yielded 3.1 gm. NMT &amp;amp; 1.3 gm. DMT.)&lt;br /&gt;
&lt;br /&gt;
[[Acacia maidenii]]&lt;br /&gt;
* 0.24% in dry bark. Fitzgerald &amp;amp; Sioumis 1965.&lt;br /&gt;
* [Tentative positive in roots as the major alkaloid. (unconfirmed) tlc by Appleseed 1994) (2 year old seed grown plants)&lt;br /&gt;
&lt;br /&gt;
[[Acacia obtusifolia]]&lt;br /&gt;
* Suspected to co-occur with DMT (tlc by Appleseed).&lt;br /&gt;
*Mulga ran hplc-ms and observed what appeared to be a simple tryptamine but was unclear if the identity was this alkaloid or tryptamine as the parent fragments seemed to be lacking; see http://www. lycaeum.org/drugsiplants/ tryptamines/acacia/species.htm &amp;amp; Trout's Notes on Acacias 2004.&lt;br /&gt;
*60% of total alkaloid in common form - D. Siebert 1997; southern Cross Uni. 2000 cited by Nen&lt;br /&gt;
&lt;br /&gt;
[[Acacia rigidula]]&lt;br /&gt;
*4.6 ppm in early spring/54.9 ppm in late fall. Fresh leaves, petioles &amp;amp; tender twigs. Clement et al. 1998&lt;br /&gt;
&lt;br /&gt;
[[Acacia simplicifolia]] [=A. simplex?]&lt;br /&gt;
*1.44% in bark and 0.29% in twigs. &lt;br /&gt;
* Stem bark has 3.6% total alkaloid content. N-Methyltryptamine (40% of total)&lt;br /&gt;
* Twigs have 0.11% total alkaloid content. N-Methyltryptamine (26.3% of total). Poupat et al. 1976 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Anadenanthera spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Anadenanthera peregrina]]&lt;br /&gt;
* No.24625; Origin: Boa Vista, Brazil]. -Traces in dry bark. (Agurell et al. 1969 ref Trout's Notes)&lt;br /&gt;
* Bark of Brazilian material (as Piptadenia). Legler &amp;amp; Tschesche 1963 reported a mixture of 5-MeO-NMT and NMT as comprising 41% of the crude base.&lt;br /&gt;
* as Piptadenia peregrina bark (Colombia in 1956). (Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Arthrophytum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum leptocladum]] M.Popov (Thin -stemmed Haloxyton)&lt;br /&gt;
* 0.575% by dry weight in 1 year old Green shoots (Flowering stage) (3.7% total alkaloid content; Major alkaloid. Cooccurring with 2 b-carbolines.) Platonova el at. 1958. ref Trout's Notes&lt;br /&gt;
* In leaf and stem. Smith 1977b cited Yurashevski 1941 Zhur. Obsch.Chem. 11:157 and Rousseau et al. 1966 Bull.Soc.Pharm.Nancy 71:31&lt;br /&gt;
&lt;br /&gt;
[[Arthrophytum wackchanica]] [A. wakhanicum?J&lt;br /&gt;
* Smith 1977b cited Orekhov 1955 ref &lt;br /&gt;
&lt;br /&gt;
=== Calycanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
Calycanthus has been listed as containing NMT. This is probably in error. Manske 1931a &amp;amp; 193lc reported NMT as a degradation product of Calycanthine. Unable to locate any reference indicating its actual presence.&lt;br /&gt;
&lt;br /&gt;
=== Delosperma spp. ===&lt;br /&gt;
&lt;br /&gt;
Presence of MMT in Delosperma spp. is unproven, except for the unpublished data involving work done by the Smith, Kline &amp;amp; French Laboratories. (Cited by Raffauf 1970). Smith 1977b cited Rivier &amp;amp; Pilet 1971 and Deulofeu 1973. Both had cited Raffauf 1970.&lt;br /&gt;
&lt;br /&gt;
* Assays by Appleseed 1994- 1996 ref Trout's Notes:&lt;br /&gt;
&lt;br /&gt;
[[Delosperma acuminatum]]&lt;br /&gt;
* Faint. Sept., Nov. 1994 and Nov. 1995 assays. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma brittenae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma cooperi]]&lt;br /&gt;
* Sept. 1994 and Nov. 1995 assays. (Ehrlich's and Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma esterhuyseniae]]&lt;br /&gt;
* Nov. 1995 assay (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hallii]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma harazianum]]&lt;br /&gt;
* Audhali Plateau, Yemen Nov. 1995 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma hirtum]]&lt;br /&gt;
* Dec. 94 (Ehrlichs) Nov. 95 assay. traces (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma klinghardtianum]]&lt;br /&gt;
* Nov. and Dec. assays. Sole base present. (Xanthydrol and Ehrlich's) Not seen Sept. 96 assay.&lt;br /&gt;
&lt;br /&gt;
[[Delosperma litorale]]&lt;br /&gt;
* Nov. 1995 assay. (Xanthydrol)&lt;br /&gt;
&lt;br /&gt;
[[Delosperma pageanum]]&lt;br /&gt;
* Same plant tested Christmas 1994) 2 Nov. 1995. Dark band (Xanthydrol)&lt;br /&gt;
* Different plant from same source) Dec. 1994 assay. (Ehrlich's)&lt;br /&gt;
&lt;br /&gt;
[[Delospemrma tradescantioides]]&lt;br /&gt;
* Nov. 1994 assay. (Ehrlich's). Suspected MMT was major. All faint.&lt;br /&gt;
&lt;br /&gt;
=== Desmanthus spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus illinoensis]]&lt;br /&gt;
* 0.11% in Root bark (dried) and 0. 0016% in Root wood (dried) Thompson et al. 1987 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Desmanthus leptobolus]]&lt;br /&gt;
* Tentative NMT presence in dried root bark (present in most but not all specimens) Appleseed tlc 1993-1994.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Diplopterys spp. === &lt;br /&gt;
[[Diplopterys cabrerana]]&lt;br /&gt;
* Traces in leaf. Agurell et al. ( 1968)a&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Girgensohnia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Girgensohnia diptera]] Bge.&lt;br /&gt;
* Yurashevski &amp;amp; Stepanov(a?) 1939 (Smith 1977b) ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Haloxylon spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Haloxylon scoparium]]&lt;br /&gt;
* Shulgin &amp;amp; Shulgin 1997&lt;br /&gt;
&lt;br /&gt;
=== Hammada spp. ====&lt;br /&gt;
&lt;br /&gt;
[[Hammada leptoclada]]&lt;br /&gt;
* In leaf and stem. Orazkulyev et at. 1964 (Grazkuliev et at. 1964 Zh. prikl.Khim. Leningr., 37: 1394; according to Arthur et at. 1967.)&lt;br /&gt;
&lt;br /&gt;
=== Hordeum vulgare ===&lt;br /&gt;
* roots of seedlings?) Schneider &amp;amp; Wightman 1974 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Justicia spp. ===&lt;br /&gt;
[[Justicia pectoralis]]&lt;br /&gt;
*In leaf. Shulgin &amp;amp; Shulgin 1997 &lt;br /&gt;
*var. stenophylla -In leaf. 31 August 1994 harvest. Faint band corresponding MMT. TLC by Appleseed ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== Mimosa spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Mimosa ophthalmocentra]].&lt;br /&gt;
* 0.0012% dry wt. in roots. Batista et al. 1999&lt;br /&gt;
* In stem Batista &amp;amp; Almeida 1997 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa scabrella]]&lt;br /&gt;
* In bark. De Moraes et al. 1990 (No quantification)&lt;br /&gt;
&lt;br /&gt;
[[Mimosa somnians]]&lt;br /&gt;
* 0.029% in dry whole plant. Gupta et al. 1979&lt;br /&gt;
&lt;br /&gt;
=== Nectandra spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Nectandra megapotamica]] (Sprg.) Chodat &amp;amp; Hassler&lt;br /&gt;
0.57 gm. from 5.7 kg. of finely powdered bark. Filho &amp;amp; Gilbert 1975&lt;br /&gt;
&lt;br /&gt;
=== Petalostylis spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Petalostylis labicheoides]]&lt;br /&gt;
* var. casseoides. This is in error [Chemical Abstracts] See Johns et al. 1966a (Included by a number of references including Mears &amp;amp; Mabry in Harbourne et al. 1971: 146)&lt;br /&gt;
&lt;br /&gt;
=== Phalaris spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Phalaris arundinacea]]&lt;br /&gt;
* cv. Ottawa Synthetic - Amounts not given. Detected by tlc. Woods &amp;amp; Clark 1971&lt;br /&gt;
&lt;br /&gt;
[[Phalaris aquatica]]&lt;br /&gt;
* cv. AQ-1 Occurence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
* Commercial) Weak occurrence reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris tuberosa]]&lt;br /&gt;
* cv. Australian Commercial - Minor alkaloid in seedlings. Mack et al. 1988&lt;br /&gt;
* A minor alkaloid in 7 day old seedlings. Mulvena &amp;amp; Slaytor 1983&lt;br /&gt;
&lt;br /&gt;
[[Phalaris paradoxa]] (Romania)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
[[Phalaris truncata]] (France)&lt;br /&gt;
* Traces reported (HPLC). Festi &amp;amp; Samorini 1994b&lt;br /&gt;
&lt;br /&gt;
=== Psychotria spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Psychotria carthaginensis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Marcos. Collected 4 Sept 1968.] Traces of NMT Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Psychotria viridis]]&lt;br /&gt;
* [&amp;quot;Rami appant'; Culina Indians, Zapote. Collected 22 July 1968]. Traces of NMT and 2-Methyl- 1,2,3,4-tetrahydro-B-carboline as minor alkaloids. Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
*&amp;quot;Kawa Kut'; Sharanahua Indians, Marcos. Collected 7 October, 1968). NMT was major alkaloid in leaf [85% of 0.11% total alkaloids by dry wt.]. DMT was absent (12% of O.11% total] Rivier &amp;amp; Lindgren 1972 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Swainsona spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Swainsona galegifolia]] (=S. coronillifolia Salisb.) &lt;br /&gt;
*(Possible assay in stem and leaf. Contradictory results.) tlc by J. Appleseed&lt;br /&gt;
&lt;br /&gt;
=== Tachigalia spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Tachigalia paniculata]] A ubi.&lt;br /&gt;
0.005% w/w of previously prepared inflorescence extract. No information on plant we ight. Svoboda et af.&lt;br /&gt;
1979&lt;br /&gt;
&lt;br /&gt;
=== Testulea spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Testulea gabonensis]]&lt;br /&gt;
* Total alkaloids in Stem bark- 2.5% and in Root bark- 5%. N-Methyltryptamine was 90% of total. Leboeuf et al. 1977 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Virola spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Snuff]]&lt;br /&gt;
*'Epena'· [No.24574; Origin: Rio Cauaburi, Brazil] - 0.014% N-Methyltryptamine: i.e. 14.3 mg. / 100 grams of sn uff. (2% of 715 mg total alkaloid per 100 gm.]&lt;br /&gt;
* &amp;quot; Nytzkwtina&amp;quot; [No . 24626; Origin: Tototobi, Brazil] - Traces Agurell et al. 1969&lt;br /&gt;
* Snuff: &amp;quot; Epena&amp;quot; ( Virola?) Snuff as prepared by Waica Indians (collected 1965). MMT (with DMT and 5-MeO-DMT]. Holmstedt &amp;amp; Lindgren 1967&lt;br /&gt;
&lt;br /&gt;
[[Virola calophylla]]&lt;br /&gt;
* [No.24603; Origin: Manaus, Brazil] Flowering shoots- 0.0077% NMT; 7.7 mg/ 100 gm (4% of 193 mg. of total alkaloids/ 100 gm. of dry flowering shoots]; Leaf- 0.0062% NMT i.e. 6.2 mg/ 100 gm [4% of 155 mg. of total alkaloids/ 100 gm. of dry leaves]. Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
*Bark collected in Manaus, Brazil during 1964. NMT (with DMT and 5-MeO-DMT). Holmstedt &amp;amp; Lindgren 1967 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Virola rufulla]]&lt;br /&gt;
* No.24612: Origin : Manaus, Brazil]. Leaf- 0.0059% i.e. 5.88 mg/ 100 gm [6% of 98 mg. of total alkaloids/ 100 gm. dry leaf]. Agurell et al. 1969&lt;br /&gt;
&lt;br /&gt;
[[Virola sebifera]]&lt;br /&gt;
* Present in bark Kawanishi et al. 1985&lt;br /&gt;
* Paste: Virola sebifera (DMK-40; Don Marcos no. I) NMT 1.38 mg/ ml. McKenna et al. 1984a&lt;br /&gt;
&lt;br /&gt;
[[Virola theiodora]]&lt;br /&gt;
* No.24595; Origin: Manaus, Brazil. Bark- 0.0025% (i.e. 2.5 mg/ 100 gm) [1% of 250 mg. of total alkaloids/ 100 gm. dry]. - Flowering shoots- 0.033% (i.e. 32.9 mg/ 100 gm) [7% of 470mg. of total alkaloids/ 100 gm. of dry flowering shoots] - Agurell et al. 1969 ref Trout's Notes&lt;br /&gt;
* Bark- 0.0034% [8 mg from 235 gm. of bark]. Cassady et al. 1972, also 1971 The latter cited Cassady et al. 1970 (Published 1972] ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Zanthoxylum spp. ===&lt;br /&gt;
&lt;br /&gt;
[[Zanthoxylum arborescens]]&lt;br /&gt;
* 0.002% in lear (dry weight) Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== Humans and other animals ===&lt;br /&gt;
&lt;br /&gt;
*Animals:&lt;br /&gt;
[[Villagorgia rubra]] (A sea fan from New Caledonia)&lt;br /&gt;
* Espada et al. 1993 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Paramuricea chamaeleon]]&lt;br /&gt;
30 mg. of NMT isolated from 200 grams of coral. Cimino&amp;amp; DeStefano 1978 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
[[Humans]]&lt;br /&gt;
* Found in cerebrospinal fluid of some psychotics and some normal people by Corbett et al. 1978. ref Trout's Notes&lt;br /&gt;
* Oon &amp;amp; Rodnight 1977 thought they observed in psychoties but did not prove.&lt;br /&gt;
* See Davis 1989 for many more references on the reported natural occurrences of N-methyltryptamine in humans:&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
30-100mg vaporised (duration 45-70 minutes), 50-180mg orally with MAOIs (duration 2-5 hours) - Nen (2001; 2011); Shulgin TIKHAL (1997)&lt;br /&gt;
&lt;br /&gt;
== Analysis of NMT ==&lt;br /&gt;
&lt;br /&gt;
=== Colorimetric reagents ===&lt;br /&gt;
&lt;br /&gt;
* [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;m=278350&amp;amp;&amp;amp;replacenum;post278350 Colorimetric reagent test results]&lt;br /&gt;
&lt;br /&gt;
=== TLC ===&lt;br /&gt;
&lt;br /&gt;
Coming soon&lt;br /&gt;
&lt;br /&gt;
=== GC-MS ===&lt;br /&gt;
&lt;br /&gt;
* Retention times for Amine 220, CHDMS and DEGS columns: Audette et al. 1969 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms.jpg]]&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:Nmtgcms2.jpg]]&lt;br /&gt;
&lt;br /&gt;
Expanded Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
MS:&lt;br /&gt;
*[http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997] HCI: (m/z) C2H6N+  44 (100%);Indolemethylene' 131 , 130 (61%, 51%); parent ion 174 (2%)&lt;br /&gt;
* Williams et al. 1971: [m/e 44, 103, 115, 130, 131, 143, 174]&lt;br /&gt;
* Holmstedt &amp;amp; Lindgren 1967: [m/e 44 (base peak), 103, 115, 130, 131, 145, 174 (M+)]. Filho &amp;amp; Gilbert 1975 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Info:&lt;br /&gt;
* GLC: Christian et al. 1975 ref Trout's Notes&lt;br /&gt;
* GLC-MS of HFB derivative: Benington et al. 1975; Vessman et al. 1969 ref Trout's Notes&lt;br /&gt;
* GC-MS: De Moraes et al. 1990 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
=== IR ===&lt;br /&gt;
&lt;br /&gt;
* Graphic portrayal. page 774 in Clarke's 1986.&lt;br /&gt;
* [http://www.erowid.org/library/books_online/tihkal/tihkal50.shtml Shulgin &amp;amp; Shulgin 1997]: Base: (cm-1): 740, 1018, 1103, 1132, 1161&lt;br /&gt;
HCl: (cm-1): 748.850, 1009, 1104. 1119, 1136&lt;br /&gt;
&lt;br /&gt;
=== NMR ===&lt;br /&gt;
&lt;br /&gt;
Cohen et al. 1960; De Moraes et al. 1990; Fi1ho &amp;amp; Gilbert 1975; Grina et al. 1982 ref Trout's Notes&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/The_Nexian_DMT_Handbook</id>
		<title>The Nexian DMT Handbook</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/The_Nexian_DMT_Handbook"/>
				<updated>2013-08-20T23:50:38Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Purification */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{ShowInfo|[[Image:Exclamation.png]]||This handbook propounds to illuminate all manner of DMT practice for informational purposes and for implementation '''only where it is legal to do so'''.  That being said, DMT's production and use should not be condoned or endorsed where it is illegal to do so.  Even where it is legal to do so, the operator must proceed with caution and in adherence to local laws, as '''many of the chemicals required for production can be hazardous to health or otherwise dangerous.'''}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{ShowInfo|[[Image:Note_error.png]]|'''Note:'''|This page is a work in progress -- its content throughout is not yet complete.}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The production and use of '''[[DMT]] (N,N-Dimethyltryptamine)''', otherwise known as '''&amp;quot;[[Spice]]&amp;quot;''', is a practice that resonates strongly with the complementary qualities of ancient shamanic and alchemical spiritual practice as well as contemporary DIY (Do It Yourself) ethic.  The production of spice is a discipline unlike that of most other commonly manufactured drugs, as it is not as well suited for bulk-production nor production for the purpose of sale as most well-known and intensively manufactured substances.  As such, its use is generally inseparable from its production in practice and in spirit.&lt;br /&gt;
&lt;br /&gt;
The production of DMT most commonly entails its extraction from botanical sources and only very rarely entails its synthesis.  In this way, its production still strongly resembles its more ancient preparations by manner of brewing, a simple form of aqueous extraction still commonly performed to this day.  This is the simplest and most readily administered form of extract if used as a component of a harmaloid-based preparation or -huasca brew.&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
Please take the time to seek further elaboration at the following resources:&lt;br /&gt;
: [http://www.dmt-nexus.me/ The DMT-Nexus]&lt;br /&gt;
: [http://deoxy.org/dmt.htm deoxy.org/dmt]&lt;br /&gt;
: [http://www.erowid.org/chemicals/dmt/ Erowid's DMT Vault]&lt;br /&gt;
: [http://en.wikipedia.org/wiki/Dimethyltryptamine Wikipedia's Article on DMT]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=='''Source Selection'''==&lt;br /&gt;
[[Image:DMT.png|thumb]]&lt;br /&gt;
DMT, its analogues, and other related alkaloids can be found in a wide variety of lifeforms, varying from trace amounts to considerable amounts. It is impossible, therefore, to include all of the sources from which DMT can be extracted, so the following discussion will focus primarily on the most commonly used and significant botanical sources.&lt;br /&gt;
&lt;br /&gt;
==='''Botanical Considerations'''===&lt;br /&gt;
&lt;br /&gt;
Several species of plants contain a variety of constituents apart from DMT. This consideration is of the utmost importance when selecting the source plant from which an extraction is to be performed, as it may become the determining factor in the material requirements of the extraction process. Some plants may even contain toxic alkaloids, so thorough research must be conducted prior to selection, extraction, and administration.&lt;br /&gt;
&lt;br /&gt;
====='''Common Botanical Sources'''=====&lt;br /&gt;
&lt;br /&gt;
{{:Mimosa hostilis}}&lt;br /&gt;
&lt;br /&gt;
{{:Diplopterys cabrerana}}&lt;br /&gt;
&lt;br /&gt;
{{:Psychotria viridis}}&lt;br /&gt;
&lt;br /&gt;
See also:&lt;br /&gt;
:[[DMT Containing Plants]]&lt;br /&gt;
:[http://dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=1123 Plants that Contain DMT forum topic]&lt;br /&gt;
&lt;br /&gt;
====='''Methods of Refinery'''=====&lt;br /&gt;
&lt;br /&gt;
Before extracting alkaloids from the variety of plants named above, one generally needs to clean and prepare the plant source, to include washing, pulverization, or any other necessary pre-treatment.  Oftentimes, plants obtained through vendors have been prepared to some extent, and only require some degree of pulverization unless obtained in pre-powdered form.  Pulverization is generally achieved by use of a household coffee grinder or a blender, though some materials must be prepared for pulverization by hand or any other method to avoid damaging the grinder.  The process can be quite messy and painstaking, depending on the material an methods used.&lt;br /&gt;
&lt;br /&gt;
====='''Defatting Concerns'''=====&lt;br /&gt;
&lt;br /&gt;
Depending on the extraction methods used, foliage will require a defatting phase in order to better facilitate a proper extraction.  This generally requires that the material undergo extraction by acidic water prior to defatting.  The product will be rendered water soluble and will remain in an aqueous phase as the solution is washed with an [[NPS]] to remove fats and oils.&lt;br /&gt;
&lt;br /&gt;
==='''Vendor Considerations'''===&lt;br /&gt;
&lt;br /&gt;
Though none of the plants containing DMT are illegal, the alkaloids contained within generally are.  Vendors generally must take it upon themselves not to advertise the illicit contents of their products, otherwise risking putting themselves and their customers in jeopardy.  Ordering these botanicals from across borders into countries where their contents are considered illegal is ill-advised but not necessarily risky, especially not if intended for legitimate use.  Always be sure to research the reputation of a vendor prior to purchase, as the potentially taboo nature of their products may inspire unethical business practice, such as unreliable delivery or poor product quality; though such cases are not necessarily specifically limited specifically to these sorts of vendors, of course.&lt;br /&gt;
&lt;br /&gt;
==='''Considerations Regarding Cultivation'''===&lt;br /&gt;
&lt;br /&gt;
Again, as these plants are usually not illegal, neither is their cultivation.  Often these plants are only native to very specific regions, thus requiring very specific growing conditions, but many can be successfully cultivated indoors or seasonally outside of their native regions.  Cultivation for the expressed or deduced purpose of refinery, use or sale of an illicit substance can result in harsh legal consequences, however.&lt;br /&gt;
&lt;br /&gt;
:[http://www.dmt-nexus.me/forum/default.aspx?g=topics&amp;amp;f=38 The Ethnobotanical Garden Forum Topic]&lt;br /&gt;
&lt;br /&gt;
=='''Extraction'''==&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Dimethyltryptamine-3d-sticks.png|thumb]]&lt;br /&gt;
&lt;br /&gt;
Extraction generally refers to the process of isolating a product from a source.  The basic idea is to utilize the unique properties of the product&amp;amp;mdash;whether reactive, electromagnetic, or otherwise structural&amp;amp;mdash;to draw it out of the source and into a target solvent.  To accomplish this the product must either be naturally soluble in the solvent or must undergo reaction to increase its solubility.  The difference between a high and low yield is firstly determined by how much more soluble the product is in the target solvent, than in its source material or solution, and secondly by how thoroughly the target solvent is mechanically brought into contact with the target solvent; this is generally determined by a combination of the droplet size and dispersion of a solvent and/or the surface area exposure and structural consistency of the source material.&lt;br /&gt;
&lt;br /&gt;
See also:&lt;br /&gt;
:[http://dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=1085 DMT Extraction Overview]&lt;br /&gt;
&lt;br /&gt;
{{:Straight-To-Base Extraction}}&lt;br /&gt;
&lt;br /&gt;
{{:Acid/Base Extraction}}&lt;br /&gt;
&lt;br /&gt;
{{:Dry Technique Extraction}}&lt;br /&gt;
&lt;br /&gt;
{{:Limtek Extraction}}&lt;br /&gt;
&lt;br /&gt;
=='''Crystallization'''==&lt;br /&gt;
&lt;br /&gt;
[[Image:Dmtx400tt9.jpg|thumb]]&lt;br /&gt;
&lt;br /&gt;
Crystallization is the process by which a product is isolated from a solvent.  This is accomplished by either allowing the solvent to completely evaporate or by causing a precipitation to occur within the solvent, which can then be isolated from the solvent by several methods and then dried of any residual solvent.&lt;br /&gt;
&lt;br /&gt;
=== Evaporation and Slow Precipitation ===&lt;br /&gt;
&lt;br /&gt;
In extraction, evaporation is the process by which a solvent disperses from its liquid form into the air as a vapor and a gas.  When this occurs, the less volatile constituents of the solvent solution are left behind, and as such, it is a common method of isolating solutes from solvent.  Typically, a solvent is evaporated in a shallow dish in order to maximize surface area exposure, often with mild heat and airflow applied to hasten the process; however, minimizing surface area and airflow and eliminating heat are often found to improve the quality of precipitate yielded by process of slow precipitation.  Many solvents are found to be limited in their ability to crystallize a product by evaporation, yielding a product ranging from oils and &amp;quot;goo,&amp;quot; to waxy crystals, to fluffy crystalline powder, to hard crystal shards.  These discrepancies in quality of yield are determined by the solvents speed of evaporation, solubility of product in the solvent, or impurities present in the solvent.&lt;br /&gt;
&lt;br /&gt;
Considerations:&lt;br /&gt;
* Many common solvents contain impurities which may not be quite as volatile as the pure solvent and may leave these impurities behind as a residue.&lt;br /&gt;
* Solvents often emit fumes and odors which may be hazardous to health, flammable, or may alarm those within proximity of the odor.&lt;br /&gt;
* Some solvents may require an excessive length of time to evaporate.&lt;br /&gt;
* Some solvents may absorb ambient moisture, resulting in a less expedient evaporation.&lt;br /&gt;
* Excessive air flow may cause the oxidization of the product.&lt;br /&gt;
* Solvent may become Trapped within the crystal structure of the product, resulting in a less solid and less pure product.&lt;br /&gt;
&lt;br /&gt;
==== Full-Range Extracting Solvents ====&lt;br /&gt;
&lt;br /&gt;
[[Xylene]]&lt;br /&gt;
&lt;br /&gt;
[[Toluene]]&lt;br /&gt;
&lt;br /&gt;
[[d-Limonene]]&lt;br /&gt;
&lt;br /&gt;
[[Dichloromethane]]&lt;br /&gt;
&lt;br /&gt;
[[Ethyl Ether]]  &lt;br /&gt;
&lt;br /&gt;
[[Chloroform]]&lt;br /&gt;
&lt;br /&gt;
==== Low-Solubility Solvents ====&lt;br /&gt;
&lt;br /&gt;
Theses solvents dissolve a much more narrow range of product and are used to isolate DMT from active and inactive impurities, alike.  However, when used for extraction, they are often heated and dissolve a bit more variance in alkaloids, and they may require further purification.&lt;br /&gt;
&lt;br /&gt;
* [[Heptane]] requires much heating to dissolve any significant concentration of product but precipitates product very easily at room temperature or cooler.  It is often found in quite pure form, reliably free of additives, and is a choice solvent for recrystallization and slow evaporation and precipitation.&lt;br /&gt;
* [[Naphtha]] can require a bit of heating to dissolve a significant concentration of product but precipitates product relatively easily at room temperature or cooler.  While never without a wide variety of additives, some brands will evaporate cleanly without leaving a residue.  This is a common solvent used for both extraction and evaporation but is often considered most preferable for [[#Freeze Precipitation|freeze precipitation]].&lt;br /&gt;
&lt;br /&gt;
==== Polar Solvents ====&lt;br /&gt;
&lt;br /&gt;
[[Acetone]]&lt;br /&gt;
[[MEK]]&lt;br /&gt;
[[IPA]]&lt;br /&gt;
&lt;br /&gt;
{{:Freeze Precipitation}}&lt;br /&gt;
&lt;br /&gt;
{{:Manual Crystallization}}&lt;br /&gt;
&lt;br /&gt;
=== Salting ===&lt;br /&gt;
&lt;br /&gt;
Salting is the process by which freebase DMT is reacted with an acid to create a salt form which is generally water-soluble.  The natural form of DMT in botanical sources tends to be a salt-form, thus facilitating the simple aqueous extraction used to prepare DMT-containing brews.  It is quite common to perform aqueous acid extractions from the material, however&amp;amp;mdash;whether for the purposes of a brew or for A/B extraction.  The salt-form itself rarely lends itself to proper crystallization and usually can only be isolated as an oil unless very specific methods and materials are employed.&lt;br /&gt;
&lt;br /&gt;
==== The Use of Fumaric Acid ====&lt;br /&gt;
&lt;br /&gt;
Few salt-forms of DMT facilitate crystallization, but DMT fumarate currently stands alone as a solid crystalline salt-form of DMT.&lt;br /&gt;
&lt;br /&gt;
{{:The FASA Method}}&lt;br /&gt;
{{:The FASW Method}}&lt;br /&gt;
{{:The FASIPA Method}}&lt;br /&gt;
&lt;br /&gt;
==== Discussion of Other Salt-Forms ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Further Elaboration and Technical Support ====&lt;br /&gt;
&lt;br /&gt;
: [http://dmt-nexus.me/forum/default.aspx?g=topics&amp;amp;f=23 Subforum on the Topic of Salting]&lt;br /&gt;
&lt;br /&gt;
=='''Purification'''==&lt;br /&gt;
&lt;br /&gt;
[[Image:SpiceCrystal001.jpg‎|thumb]]&lt;br /&gt;
&lt;br /&gt;
The purification of DMT product has several purposes and is accomplished by several different methods, but all of them essentially involve the washing of product in some way or another.  Purification either involves the isolation of product from unwanted impurities from the plant source or from the process of extraction, or it involves the isolation of product from active impurities which may or may not be collected after isolation.&lt;br /&gt;
&lt;br /&gt;
==='''Recrystallization'''===&lt;br /&gt;
&lt;br /&gt;
The general purpose of recrystallization is to crystallize the product in a fresh solvent after it has already been isolated from the extraction solvent, likely containing a considerable amount of impurities.  In this technique, an impure solid compound is dissolved in a solvent and then allowed to slowly crystallize out as the solution cools.  Often this process results in more well-formed crystals with less discoloration. The advantage of this method of purification is that the solvent choice for recrystallization may be different and more suitable than that chosen for extraction.  Crystallization of a solid relies on slow, selective formation of the crystal lattice and is quite different from precipitation. In freeze precipitation, there is a rapid formation of a solid from a solution that causes impurities to be trapped within the solid's crystal framework. For this reason, extractions that rely on precipitation or evaporation to produce a solid product always include a final recrystallization step to give the pure compound.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The process of recrystallization relies on the property that for most compounds, as the temperature of a solvent increases, the solubility of the compound in that solvent also increases. For example, much more sugar can be dissolved in very hot water (just below boiling) than in water at room temperature. Inversely, if a hot saturated solution of sugar and water is allowed to cool, sugar will begin to crystallize out of solution as solubility decreases. Recrystallization will give your product a more sharply defined, uniform melting point and in the case of DMT allow for hard non-waxy crystals.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
 &lt;br /&gt;
{{Procedure|Removing Inactive Impurities via Recrystallization|&lt;br /&gt;
&lt;br /&gt;
{{materials_list&lt;br /&gt;
|&lt;br /&gt;
* '''Freebase DMT''' &lt;br /&gt;
|&lt;br /&gt;
* '''Heptane'''&lt;br /&gt;
|&lt;br /&gt;
* '''Activated Charcoal (eg. Norit)'''&lt;br /&gt;
|&lt;br /&gt;
* '''Filter papers, Beakers, Waterbath, Pipette '''}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
# ''Find a suitable solvent for the recrystallization;''&lt;br /&gt;
# ''Dissolve the impure solid in a minimum volume of hot solvent;''&lt;br /&gt;
# ''Remove any insoluble impurities by filtration;''&lt;br /&gt;
# ''Slowly cool the hot solution to crystallize the desired compound from the solution.''}}&lt;br /&gt;
&lt;br /&gt;
==== Finding a suitable solvent ====&lt;br /&gt;
The first consideration in purifying a solid by recrystallization is to find a suitable solvent. A good recrystallization solvent should fit the following criteria:&lt;br /&gt;
&lt;br /&gt;
1. The compound should be very soluble at the boiling point of the solvent and only sparingly soluble in the solvent at room temperature.&lt;br /&gt;
&lt;br /&gt;
2. The unwanted impurities should be insoluble in the hot solvent. &lt;br /&gt;
&lt;br /&gt;
A good recrystallization solvent for DMT is [[heptane]]. DMT is not very soluble in it at room temperature but quite soluble as we add heat. Most common spice impurities, however, are not very soluble in it at all and can thus be separated via simple decanting.&lt;br /&gt;
&lt;br /&gt;
==== Dissolve solid into hot solvent ====&lt;br /&gt;
Prepare a waterbath and heat the DMT and the heptane in their own beakers until the DMT begins to melt. Add heated solvent dropwise into the beaker containing the extract. The heptane will go cloudy almost immediately and take on a yellow color as the DMT goes into solution. Keep adding heated solvent until further addition or agitation causes no more DMT to dissolve. &lt;br /&gt;
&lt;br /&gt;
Your beaker should now contain yellowish-tinged heptane with an orange-brown blob of oil and undissolved solids at the bottom of the vessel. Carefully decant the solution into another beaker, careful to leave the impurities behind. Repeat dropwise addition of heated solvent and decantation to ensure no DMT is left behind. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Decolorize with carbon ==== &lt;br /&gt;
Now that we have dealt with insoluble impurities, our solution is see-through but tinged yellow. This discoloration is due to the presence of high-molecular-weight reaction by-products which may have been formed during the extraction process. A simple wash with activated carbon will get rid of decolorizing compounds. (Activated carbon is extremely efficient at absorbing impurities due to its large surface area.) &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1. Add excess solvent and activated carbon, and boil the solution for a few minutes.  The colored impurities will adsorb onto the surface of activated charcoal.&lt;br /&gt;
&lt;br /&gt;
2. Remove the charcoal with absorbed impurities by filtration. Your solvent should now be almost clear. If the yellow color persists, repeat the charcoal wash carefully. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Note: Very little activated carbon is needed to remove the colored impurities from a solution. You must be careful in your use of decolorizing carbon: if too much is used, it can adsorb the desired compound from the solution as well as the colored impurities.'''&lt;br /&gt;
&lt;br /&gt;
==== Crystallization ==== &lt;br /&gt;
After the solution has been filtered cover the flask containing the hot filtrate and set it aside undisturbed to cool slowly to room temperature. As the solution cools, the solubility of the dissolved compound will decrease and the solid will begin to crystallize from the solution. Once the solution reaches room temperature, move it into the refridgerator, and finally into the freezer to freeze precipitate most of the DMT. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''The slower your solution cools, the cleaner and larger your crystals will be.'' '''&lt;br /&gt;
&lt;br /&gt;
==== Further Reading ====&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.wikihow.com/Crystallize-Organic-Compounds How to Crystallize Organic Compounds - WikiHow]&lt;br /&gt;
&lt;br /&gt;
[http://loinen.i2p.to/rhodium/chemistry/equipment/recrystallization.html Recrystallization Technique - Rhodium]&lt;br /&gt;
[[Category:Enhancement Tek]]&lt;br /&gt;
[[Category:Harm reduction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{:Washing Spice}}&lt;br /&gt;
&lt;br /&gt;
==='''Freebase Conversion from Salt'''===&lt;br /&gt;
&lt;br /&gt;
The methods used for converting crystalline salt-form DMT into freebase are not dissimilar from those used in extraction.  The only significant difference between the processes is that the conversion involves far fewer impurities and less material than the extraction.  Because of of this and the fact that it involves the isolation of the product from an acid, the conversion acts as a sort of purification method.&lt;br /&gt;
&lt;br /&gt;
{{:Drytek Freebase Conversion of DMT}}&lt;br /&gt;
&lt;br /&gt;
{{:Crystalline Freebase Conversion of DMT}}&lt;br /&gt;
&lt;br /&gt;
{{:Nontoxic Freebase Spice Conversion}}&lt;br /&gt;
&lt;br /&gt;
{{:STB Freebase Conversion of DMT}}&lt;br /&gt;
&lt;br /&gt;
====='''Further Elaboration and Technical Support'''=====&lt;br /&gt;
&lt;br /&gt;
: [[:Category:Conversion Tek|Directory of Conversion Teks]]&lt;br /&gt;
: [http://www.dmt-nexus.me/forum/default.aspx?g=topics&amp;amp;f=23 Forum on the Topic of FASA]&lt;br /&gt;
&lt;br /&gt;
=='''Administration'''==&lt;br /&gt;
&lt;br /&gt;
{{:Leaf Enhancement}}&lt;br /&gt;
&lt;br /&gt;
==='''Vaporization'''===&lt;br /&gt;
&lt;br /&gt;
The vaporization method of administration pertains to the use of pure freebase product with no additional material.  This method generally makes use of heating an apparatus that is intended to distribute the heat to the product until it reaches the point of vaporization and can be inhaled.&lt;br /&gt;
&lt;br /&gt;
====='''Glass-Pipe Vaporizers'''=====&lt;br /&gt;
&lt;br /&gt;
Glass-pipe vaporizers are glass pieces that are meant to be heated directly in order to indirectly disperse that heat into the product.  The glass used must be thin enough for the heat to pass through its structure and potentially distribute the heat evenly.  The piece must have a chamber within which the product will undergo vaporization.  It must be assembled in a manner that will allow for air intake and output:  The output being the inhalation nozzle, and the input being a sort of carb.&lt;br /&gt;
&lt;br /&gt;
{{procedure&lt;br /&gt;
|the Improvisation of a Glass Pipe Vaporizer&lt;br /&gt;
|&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
{{:The Machine}}&lt;br /&gt;
&lt;br /&gt;
====='''Effective Use and Maintenance'''=====&lt;br /&gt;
&lt;br /&gt;
As the term indicates, vaporizers are intended to vaporize, not to burn product, as such, the product should never come into contact with the flame or be overly heated to the point of burning.  Generally, a vacuum must be generated in order to direct the heat through the product and to direct the vapor into the chamber.  Which should not be allowed to sit for too long, as it may begin to precipitate within the chamber.  Every toke should be held in the lungs as long as necessary for the vapor to be completely absorbed, as no vapor should be exhaled.&lt;br /&gt;
&lt;br /&gt;
Heat-Source:&lt;br /&gt;
: Though many prefer a butane torch  for expedient heating, and though many manners of vaporizer demand its use, a standard lighter will produce adequate heat for vaporization.  A standard lighter is generally ideal for vaporizers that generate a strong enough vacuum to pull the flame toward the heat sink.&lt;br /&gt;
&lt;br /&gt;
Common Methods of Inhalation:&lt;br /&gt;
* Some prefer to vaporize their entire dose before inhaling so as to administer one strong toke.  This method can be quite harsh and difficult on the lungs and throat and may induce coughing.  However, this is reportedly the most intense method of administration, almost always inducing a &amp;quot;breakthrough&amp;quot; if held in the lungs for adequate absorption.&lt;br /&gt;
* Others prefer to administer one dose within multiple tokes, which is reportedly slightly longer-lasting and much easier on the lungs and throat though possibly less intense.  Usually the amount of tokes taken depends on the intended depth of the experience.  In many cases, three is found to be more than adequate and four is said to be a &amp;quot;breakthrough&amp;quot; dose.  Any subsequent tokes to the first toke must occur within the first minute, due to both tolerance and lack of motor skills building up rapidly&lt;br /&gt;
&lt;br /&gt;
Cleaning the Apparatus:&lt;br /&gt;
* The apparatus used for vaporization can be cleaned using the same solvents used for extraction.  However, volatility and toxicity concerns should be a strong consideration in choosing the proper solvent.&lt;br /&gt;
* It is preferable to choose a solvent that evaporates quickly and cleanly and able to dissolve a broad range of products, as oxidization is likely to have occurred.&lt;br /&gt;
* Residual solvent residue may be hazardous, as the user may inhale harmful fumes or potentially ignite the solvent.&lt;br /&gt;
&lt;br /&gt;
: The residual product dissolved by the cleaning solvent may be salvaged by appropriate methods of crystallization.  However, it is likely to contain a variety of inactive constituents, so proper purification measures would be advisable.&lt;br /&gt;
&lt;br /&gt;
====='''Concerns Regarding the Experience'''=====&lt;br /&gt;
&lt;br /&gt;
* The primary effects of smoked DMT, induced within minutes of administration, last for about 5-10 minutes and are characterized by strong visual hallucination, a strong psychedelic quality, and minor auditory hallucination, while the secondary effects of a much more mild character may last for up to an hour.&lt;br /&gt;
* Tolerance is reportedly induced rapidly and often dissipates rapidly, though repeated or high doses may induce a slightly longer term tolerance. Some believe it is best to wait at least one hour between doses.&lt;br /&gt;
* The experience of smoking DMT is said to be quite overwhelming.  It is often necessary for the user to have a &amp;quot;sitter&amp;quot; nearby to tend to the smoking apparatus so as to not risk the possibility of the user damaging it or accidentally inflicting burns.  It can also be temporarily debilitating, so the user may be advised to refrain from any physical activity.&lt;br /&gt;
* Set and setting are of the utmost importance, as the user is often rendered temporarily vulnerable and emotionally fragile.  The user must determine the appropriate conditions in which administration is to take place but is advised to initially seek out a setting containing minimal stimuli.&lt;br /&gt;
* It may also behoove the user to seek out a more experienced sitter for guidance and support.  Often this is unavailable, and as such, it would be more advisable for the user to perform the rite in solitude.  An inexperienced sitter may inadvertently induce anxiety in the user out of negligence or unnecessary concern.&lt;br /&gt;
&lt;br /&gt;
====='''Further Elaboration and Technical Support'''=====&lt;br /&gt;
&lt;br /&gt;
: [http://forums.mycotopia.net/attachments/botanicals-cactus-misc-entheogens-psychedelics/67822d1195320961-dmt-pipe-83484machine.jpg &amp;quot;The Machine&amp;quot; Article from The Entheogen Review]&lt;br /&gt;
&lt;br /&gt;
==='''Potentiation'''===&lt;br /&gt;
&lt;br /&gt;
: The effects of DMT, as with most psychedelic substances, can be lengthened, strengthened, altered, or otherwise potentiated through the use of various psychoactive or bioactive compounds.  The potentiation of DMT is actually the oldest method of administration, as its necessarily potentiated oral administration serves as the compound's longest known history of use.  DMT is generally considered to be orally inactive without some form of potentiation, such as a harmaloid preparation.  DMT's potentiation is not limited to oral use, however, as many of the same potentiating agents may be used in conjunction with vaporized or otherwise administered DMT.&lt;br /&gt;
&lt;br /&gt;
{{:Harmaloids}}&lt;br /&gt;
&lt;br /&gt;
{{:Jungle Spice}}&lt;br /&gt;
&lt;br /&gt;
====='''Further Potentiation'''=====&lt;br /&gt;
&lt;br /&gt;
=='''Appendices'''==&lt;br /&gt;
&lt;br /&gt;
==='''Storage Concerns'''===&lt;br /&gt;
: DMT should be stored in a cool and dry place, preferably in a sealed container.&lt;br /&gt;
&lt;br /&gt;
{{:DMT N-Oxide}}&lt;br /&gt;
&lt;br /&gt;
=== Analogues ===&lt;br /&gt;
&lt;br /&gt;
{{:5-MeO-DMT}}&lt;br /&gt;
&lt;br /&gt;
{{:Bufotenin}}&lt;br /&gt;
&lt;br /&gt;
=== References ===&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|The Nexian DMT Handbook|DMT}}&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-17T00:42:34Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* Mental: paranoia, fear, and panic. No other known specific physical risks at this time (but likely similar to LSD).&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published about, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:43:51Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* Mental: paranoia, fear, and panic. No other known specific physical risks at this time (but likely similar to LSD).&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:42:41Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* mental: paranoia, fear, and panic. No other known risks at this time (likely similar to LSD).&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:41:45Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* paranoia, fear, and panic, no other known risks at this time (likely similar to LSD).&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:41:08Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* paranoia, fear, and panic, no other known risks at this time&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:40:10Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* paranoia, fear, and panic&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-08-16T22:30:58Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Safety_profile&lt;br /&gt;
|&lt;br /&gt;
* Psychedelic&lt;br /&gt;
|&lt;br /&gt;
* Open and closed eye visuals, euphoria, change in perception of time&lt;br /&gt;
|&lt;br /&gt;
* Nausea, vasoconstriction (mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing&lt;br /&gt;
|&lt;br /&gt;
* paranoia, fear, and panic, dystonia (rare), seizure (rare), death (rare)&lt;br /&gt;
|&lt;br /&gt;
* AL-LAD is a substance with very little published used, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known. &lt;br /&gt;
* Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD and potential long-term effects. As with any RC, caution should be exercised.&lt;br /&gt;
No deaths or hospitalizations have been reported due to it's usage so far (august 2013) there is no data for lasting negative physical effect.&lt;br /&gt;
&lt;br /&gt;
AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect.  This chemical is a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented it can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
http://www.ecstasydata.org/view.php?ID=2829&lt;br /&gt;
[[File:Al lad spectra.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-06-22T20:47:53Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Pharmacology, toxicity and general safety */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
DOSAGE : 80 - 160 micrograms +. &lt;br /&gt;
&lt;br /&gt;
DURATION : 6 - 8 hours.&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD. AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect. No deaths have been reported due to it's usage and so far there is no data for lasting negative physical effect. This chemical is still a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented and can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-06-22T20:43:19Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Pharmacology, toxicity and general safety */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD. AL-LAD is every bit as much as potent as it's sister molecule LSD and should be treated with equal respect. No deaths have been reported due to it's usage and so far there is no data for lasting negative physical effect. This chemical is still a powerful psychedelic and the effects are mostly mental/visual. Most online reports have been positive with no complaints of negative physical effect after the experience has ran its course. &lt;br /&gt;
&lt;br /&gt;
Bad trips are always possible with almost any psychedelic and AL-LAD is no exception, with reports mentioning things becoming much too intense and 'cartoon like' at higher dosages. Always make sure you know how much you are ingesting and do so in a safe environment where you feel comfortable. NEVER ingest a psychedelic if you will be working or driving.&lt;br /&gt;
&lt;br /&gt;
There scarce data regarding the combination of AL-LAD and other substances. Combination with MAOIs (monoamine oxidase inhibitors) carries the same risk as with many other psychedelics, however since this combination has not been documented and can NOT be recommended at this point.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-06-22T20:21:40Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Chemical and physical properties */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is a 6-alkylated analogue of nor-LSD.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD, safety guidelines would be similar to that of LSD as the potency is roughly the same.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-06-22T20:19:20Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Brief overview - What is AL-LAD? */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It closely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
Very similar to LSD, AL-LAD is on of a series of 5-alkylated analogues of nor-LSD (TIHKAL).&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD, safety guidelines would be similar to that of LSD as the potency is roughly the same.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/AL-LAD</id>
		<title>AL-LAD</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/AL-LAD"/>
				<updated>2013-06-22T20:11:22Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: AL-LAD entry&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:AL-LAD.png|right|thumb|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Brief overview - What is AL-LAD? ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD novel hallucinogenic developed originally by David E. Nichols and popularized by Alexander Shulgin. It losely resembles LSD in chemical structure and has very similar dosages and effects.&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&lt;br /&gt;
&lt;br /&gt;
Very similar to LSD, AL-LAD is on of a series of 5-alkylated analogues of nor-LSD (TIHKAL).&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
Effects can be felt within a quarter hour to an hour or more. Physically the experience can include a warm body high, elevated heart rate and increased energy. Visually the effects are similar to that of LSD (depending on the individual). Users often report euphoria and music enhancement. Some users report a merge between audio and visual aspects of the experience.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
Very little is known at this stage about the toxicity of AL-LAD, safety guidelines would be similar to that of LSD as the potency is roughly the same.&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
AL-LAD is easily dissolved onto blotters or can be taken in suspension, held under the tongue or on the gum and cheek. Anecdotal reports mention this compound being active orally, unlike LSD itself. A mild dose can be as low as 80 micrograms, with a intermediate dosages around 150-200 micrograms. Higher dosages have been reported up to 300 and 400 micrograms.  &lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
There is not a much credible data because of the scarcity of this compound, however Alexander Shulgin has written an extensive report of his own self experimentation in TIHKAL entry #1.&lt;br /&gt;
&lt;br /&gt;
== Analysis of AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
== Scientific publications ==&lt;br /&gt;
&lt;br /&gt;
== Other links of interest ==&lt;br /&gt;
&lt;br /&gt;
https://www.dmt-nexus.me/Files/Books/General/%28ebook%29Tihkal.pdf&lt;br /&gt;
&lt;br /&gt;
{{Page Footer|Allies and Associated Alkaloids}}&lt;br /&gt;
[[Category:Alkaloids]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/Category:Alkaloids</id>
		<title>Category:Alkaloids</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/Category:Alkaloids"/>
				<updated>2013-06-22T19:39:50Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: /* Ergolines */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Note: Some substances listed here are not alkaloids due to lack of nitrogen (for example cannabinoids).&lt;br /&gt;
&lt;br /&gt;
Click on the substance name below for individual WIKI and detailed information on each substance.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
= Tryptamines = &lt;br /&gt;
&lt;br /&gt;
Substances based on the tryptamine structure &lt;br /&gt;
&lt;br /&gt;
== Tryptamine ==&lt;br /&gt;
[[Image:Tryptamine_structure.png]]&lt;br /&gt;
&lt;br /&gt;
* [[Tryptamine]]&lt;br /&gt;
&lt;br /&gt;
== DMT ==&lt;br /&gt;
[[Image:dmtfreebase.png|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[DMT]]&lt;br /&gt;
&lt;br /&gt;
== DMT N-Oxide ==&lt;br /&gt;
[[Image:dmtnoxide.jpg|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[DMT N-Oxide]]&lt;br /&gt;
&lt;br /&gt;
== NMT ==&lt;br /&gt;
[[Image:Nmt.jpg|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[NMT]]&lt;br /&gt;
&lt;br /&gt;
== Psilocin (4-HO-DMT) and psilocybin (4-PO-DMT) ==&lt;br /&gt;
[[Image:psilocinfreebase.png|150px]]&lt;br /&gt;
[[Image:psilocybin.png|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[Psilocin and Psilocybin]]&lt;br /&gt;
&lt;br /&gt;
== Bufotenin (5-HO-DMT)==&lt;br /&gt;
&lt;br /&gt;
[[Image:bufoteninefreebase.png|150px]]&lt;br /&gt;
* [[Bufotenine]]&lt;br /&gt;
&lt;br /&gt;
== Bufotenine N-Oxide ==&lt;br /&gt;
&lt;br /&gt;
* [[Bufotenine N-Oxide]]&lt;br /&gt;
&lt;br /&gt;
== 5-MeO-DMT ==&lt;br /&gt;
&lt;br /&gt;
[[Image:5meodmtfreebase.png|150px]]&lt;br /&gt;
* [[5-MeO-DMT]]&lt;br /&gt;
&lt;br /&gt;
== 5-MeO-DMT N-Oxide ==&lt;br /&gt;
&lt;br /&gt;
[[Image:5meodmtoxide.png|150px]]&lt;br /&gt;
* [[5-MeO-DMT N-Oxide]]&lt;br /&gt;
&lt;br /&gt;
== 5-MeO-NMT ==&lt;br /&gt;
&lt;br /&gt;
[[Image:5meonmt.png|150px]]&lt;br /&gt;
* [[5-MeO-NMT]]&lt;br /&gt;
&lt;br /&gt;
== Yuremamine ==&lt;br /&gt;
&lt;br /&gt;
* [[Yuremamine]]&lt;br /&gt;
&lt;br /&gt;
== Other tryptamines ==&lt;br /&gt;
&lt;br /&gt;
Tryptamine analogues&lt;br /&gt;
&lt;br /&gt;
[[Image:Tryptamineanalogues.jpg]]&lt;br /&gt;
&lt;br /&gt;
= Beta-Carbolines = &lt;br /&gt;
&lt;br /&gt;
Substances based on the cyclic beta carboline structure&lt;br /&gt;
&lt;br /&gt;
[[File:Betacarboline.png]]&lt;br /&gt;
&lt;br /&gt;
== Harmine ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Harminefreebase.png|150px]]&lt;br /&gt;
* [[Harmine]]&lt;br /&gt;
&lt;br /&gt;
== Harmaline ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Harmaline.png|150px]]&lt;br /&gt;
* [[Harmaline]]&lt;br /&gt;
&lt;br /&gt;
== Tetrahydroharmine ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Thhfreebase.png|150px]]&lt;br /&gt;
* [[Tetrahydroharmine]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Harman / Harmane ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Harman.jpg|150px]]&lt;br /&gt;
* [[Harman]]&lt;br /&gt;
&lt;br /&gt;
== MTHBC / Tetrahydroharman ==&lt;br /&gt;
&lt;br /&gt;
(1-Methyl-1,2,3,4-Tetrahydro-Beta-Carboline)&lt;br /&gt;
&lt;br /&gt;
[[Image:Mthbc.jpg|150px]]&lt;br /&gt;
* [[MTHBC]]&lt;br /&gt;
&lt;br /&gt;
== 2-MTHBC ==&lt;br /&gt;
&lt;br /&gt;
(2-Methyl-1,2,3,4-Tetrahydro-Beta-Carboline)&lt;br /&gt;
&lt;br /&gt;
[[Image:2mthbc.gif|150px]]&lt;br /&gt;
* [[2-MTHBC]]&lt;br /&gt;
&lt;br /&gt;
== Other beta-carbolines and analogues ==&lt;br /&gt;
&lt;br /&gt;
= Phenetylamines = &lt;br /&gt;
&lt;br /&gt;
== Mescaline ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Mescalinefreebase.png|150px]]&lt;br /&gt;
* [[Mescaline]]&lt;br /&gt;
&lt;br /&gt;
== MDMA ==&lt;br /&gt;
&lt;br /&gt;
[[Image:Mdma.png|150px]]&lt;br /&gt;
* [[MDMA]]&lt;br /&gt;
&lt;br /&gt;
== 2C-x compounds ==&lt;br /&gt;
&lt;br /&gt;
* [[2C-x]]&lt;br /&gt;
* [[2C-B]]&lt;br /&gt;
&lt;br /&gt;
== DO-x compounds ==&lt;br /&gt;
&lt;br /&gt;
* [[DO-x]]&lt;br /&gt;
* [[DOM]]&lt;br /&gt;
&lt;br /&gt;
== Cathinone and analogues ==&lt;br /&gt;
&lt;br /&gt;
* [[Cathinone and analogues]]&lt;br /&gt;
&lt;br /&gt;
== Ephedrine and analogues ==&lt;br /&gt;
&lt;br /&gt;
* [[Ephedrine and analogues]]&lt;br /&gt;
&lt;br /&gt;
== Amphetamine and analogues ==&lt;br /&gt;
&lt;br /&gt;
* [[Amphetamine and Analogues]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
= Ergolines =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== LSD ==&lt;br /&gt;
&lt;br /&gt;
[[Image:lsd.png|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[LSD]]&lt;br /&gt;
&lt;br /&gt;
== AL-LAD ==&lt;br /&gt;
&lt;br /&gt;
[[Image:AL-LAD.png|150px]]&lt;br /&gt;
&lt;br /&gt;
* [[AL-LAD]]&lt;br /&gt;
&lt;br /&gt;
== LSA ==&lt;br /&gt;
&lt;br /&gt;
[[Image:lsafreebase.png|150px]]&lt;br /&gt;
* [[LSA]]&lt;br /&gt;
&lt;br /&gt;
== LSH ==&lt;br /&gt;
&lt;br /&gt;
* [[LSH]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Other ergolines ==&lt;br /&gt;
&lt;br /&gt;
* [[Other ergolines]]&lt;br /&gt;
&lt;br /&gt;
= [[Dissociative]]s =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Main page: [[Dissociative]]&lt;br /&gt;
&lt;br /&gt;
[[File:Other_Arylcyclohexylamine_Structures.png]]&lt;br /&gt;
&lt;br /&gt;
== Arylcyclohexylamines ==&lt;br /&gt;
&lt;br /&gt;
=== Ketamine &amp;amp; Related Analogues===&lt;br /&gt;
&lt;br /&gt;
* [[Ketamine]]&lt;br /&gt;
&lt;br /&gt;
* [[NEK]] - N-ethylnorketamine&lt;br /&gt;
&lt;br /&gt;
* [[2-MeO-KET]] - 2-methoxy-ketamine&lt;br /&gt;
&lt;br /&gt;
=== Methoxetamine, MXE ===&lt;br /&gt;
&lt;br /&gt;
* [[MXE]] - 3-MeO-2-Oxo-PCE&lt;br /&gt;
&lt;br /&gt;
=== Phenylcyclidine, PCP &amp;amp; Related Analogues ===&lt;br /&gt;
&lt;br /&gt;
* [[PCP]] - Phencyclidine&lt;br /&gt;
&lt;br /&gt;
* [[PCE]] - Eticyclidine&lt;br /&gt;
&lt;br /&gt;
* [[3-MeO-PCP]] - 3-methoxy-phenylcyclidine&lt;br /&gt;
&lt;br /&gt;
* [[4-MeO-PCP]] - Methoxydine &lt;br /&gt;
&lt;br /&gt;
* [[3-MeO-PCE]] - See PCE&lt;br /&gt;
&lt;br /&gt;
* [[3-MeO-PCPr]] - N-propyl homologue of 3-MeO-PCE&lt;br /&gt;
&lt;br /&gt;
* [[3-MeO-PCPy]] - See Rolicyclidine&lt;br /&gt;
&lt;br /&gt;
==Morphinans, κ-Opioid, others==&lt;br /&gt;
&lt;br /&gt;
* [[DXM]]&lt;br /&gt;
&lt;br /&gt;
* [[Nitrous Oxide]]&lt;br /&gt;
&lt;br /&gt;
* [[Diethyl ether]]&lt;br /&gt;
&lt;br /&gt;
* [[Xenon]]&lt;br /&gt;
&lt;br /&gt;
* [[Ibogaine]]&lt;br /&gt;
&lt;br /&gt;
* [[Salvinorin]]&lt;br /&gt;
&lt;br /&gt;
= Other plant-based psychoactives =&lt;br /&gt;
&lt;br /&gt;
== Ibogaine ==&lt;br /&gt;
&lt;br /&gt;
* [[Ibogaine]]&lt;br /&gt;
&lt;br /&gt;
== Voacangine ==&lt;br /&gt;
&lt;br /&gt;
* [[Voacangine]]&lt;br /&gt;
&lt;br /&gt;
== Muscimol and ibotenic acid ==&lt;br /&gt;
&lt;br /&gt;
* [[Muscimol and ibotenic acid]]&lt;br /&gt;
&lt;br /&gt;
== Salvinorin ==&lt;br /&gt;
&lt;br /&gt;
* [[Salvinorin]]&lt;br /&gt;
&lt;br /&gt;
== Cannabinoids ==&lt;br /&gt;
&lt;br /&gt;
* [[Natural Cannabinoids]]&lt;br /&gt;
* [[Synthetic Cannabinoids]]&lt;br /&gt;
&lt;br /&gt;
= Other compounds of interest =&lt;br /&gt;
&lt;br /&gt;
== Gramine ==&lt;br /&gt;
&lt;br /&gt;
* [[Gramine]]&lt;br /&gt;
&lt;br /&gt;
== Vasicine, vasicinone and deoxyvasicine ==&lt;br /&gt;
&lt;br /&gt;
* [[Vasicine, Vasicinone and Deoxyvasicin]]&lt;br /&gt;
&lt;br /&gt;
== Hordenine ==&lt;br /&gt;
&lt;br /&gt;
* [[Hordenine]]&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/File:AL-LAD.png</id>
		<title>File:AL-LAD.png</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/File:AL-LAD.png"/>
				<updated>2013-06-22T19:35:40Z</updated>
		
		<summary type="html">&lt;p&gt;Orion: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Orion</name></author>	</entry>

	</feed>