ACRB Tek By Thick-Light - Revision history

Bloodysafety: /* Ingredients */

2014-08-23T00:40:21Z

‎Ingredients

--Shadow at 12:42, 24 April 2014

2014-04-24T12:42:34Z

--Shadow at 12:37, 24 April 2014

2014-04-24T12:37:36Z

--Shadow at 12:26, 24 April 2014

2014-04-24T12:26:38Z

--Shadow: Created page with "#REDIRECT https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030 Step1 500 gram of ACRB, freeze/thaw twice Step2 Boil in 2000ml of water with 100ml white vinegar for 1.5..."

2014-04-24T12:25:38Z

Created page with "#REDIRECT https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030 Step1 500 gram of ACRB, freeze/thaw twice Step2 Boil in 2000ml of water with 100ml white vinegar for 1.5..."

New page

#REDIRECT https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030

Step1
500 gram of ACRB, freeze/thaw twice
Step2
Boil in 2000ml of water with 100ml white vinegar for 1.5 hrs, then transfer liquid to another pot and start reducing it
Step3
repeat step2 at least 4 times, adding fresh vinegar each time
Step4
reduce total liquid volume to around 1500ml, then let cool and pour into your extraction vessel. (A half gallon mason jar works well).
Step5
Slowly add 150g of NaOh and stir.
Step6
While the liquid is still warm, add 600ml of naptha, cap the extraction vessel, and with gloves and goggles on, shake it over a sink vigourously. Do this 6-10 times, letting the naptha and soup completely separate between agitation. On your last shake, roll the naptha around the jar lightly to reduce emulsions.
Step7
Be patient and let the solvent completely seperate from the liquid even the red lines that drip down the side. Once it's seperated decant the naptha and put in a clean dry collection jar. You should end up with a milky white opaque solvent that's very cloudy.
Step8
Leave the jar to sit for 6-8 hours and the overly saturated naptha should start to drop the DMT and leave a thick layer of needle like crystals across the bottom and sides. Get another jar that's clean and dry and pour off the solvent into it. Let the crystals dry then scrape them up and spread them out on a baking dish. once these don't smell like naptha they are ok to smoke.
Step9
The solvent you poured off should be put in a freezer for 24-48 hours so all the goodies can be freeze precipitated. Once this happens, pour the solvent off then back into the basified ACRB soup. Scrape the crystals from the jar once they are dry.
Step10
repeat shaking the jar with the naptha and a. confusa soup 6-10 times letting it seperate then shake it again etc... If the solvent is still cloudy white let it sit 6-8 hours and the saturated dmt should crystalize inside the solvent. If it doesn't then it's not saturated enough.

If that's the case let the naptha evap half way then stick it in the freezer and let it freeze precipitate. 24-48 hors. at this point pour off the solvent and let the crystals dry then scape them up wait til the naptha smell is gone and enjoy!!!!

Additional notes/tips:::
* Keep the jar in a heat bath the whole time you are doing pulls that way the naptha will stay warm and stay saturated until you decant it. plug the sink run hot water add a kettle of boiling water every 15-20 minutes or when it starts getting cool.
* filtering the final boils before basing results in a less than likely chance of ending up with dirty naptha...
* I have done up to ten pulls and got spice on every single one. If you don't take the time to shake and let the nps separate at least 6 times on your first pull it may not contain enough spice to allow room temp crystallization in the solvent. In experiments the 2nd and 3rd pull sometimes drop more crystals when freeze precipitated if the first pull is only allowed to mix and sep. 3 times. Generally the later pulls produce a sandy colored powder with beige crystals. Upon re-x this sandy powder produces a chalky pure white powder and a tan goo that dries to a peachy tan. I assume it's nmt but i'm not sure. Some should be sent out for a alk profile so we know for sure what it is.
* I also boiled the root bark first then froze it boiled it again then froze again, then while it was soft from the second boil I used a blender to shred it up almost to powder. I'm not sure if the freezing is essential but it helps to break the bark apart as the water expands and cracks the bark.
* No vodka powder or vinegar when i was freezing it. I actually soaked it in water then poured it off in the pot I was using for the boils then froze and thawed it 2x before cooking.
* didn't powder my bark due to the pains of filtering all the sediment as your doing consecutive boils.

@@ Line 5: / Line 5: @@
 * 10 litres water
 * 500ml white vinegar
-* 150g NaOh (Sodium Carbonate)
+* 150g NaOh (Sodium Hydroxide)
 * Naptha (Non-polar solvent)

@@ Line 1: / Line 1: @@
 {{ShowInfo|[[Image:Note_error.png]]|'''Note:'''|This page is a transcription of ACRB Tek By Thick-Light<ref>ACRB Tek By Thick-Light[https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030]</ref>. The content is to remain accurate as such.}}
 ==Step1==
@@ Line 25: / Line 32: @@
-==Additional notes/tips:::==
+==Additional notes/tips==
 * Keep the jar in a heat bath the whole time you are doing pulls, that way the naptha will stay warm and stay saturated until you decant it. Plug the sink, run hot water; add a kettle of boiling water every 15-20 minutes or when it starts getting cool.
 * Filtering the final boils before basing, results in a less than likely chance of ending up with dirty Naptha.

@@ Line 1: / Line 1: @@
-#REDIRECT https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030
+{{ShowInfo|[[Image:Note_error.png]]|'''Note:'''|This page is a transcription of ACRB Tek By Thick-Light<ref>ACRB Tek By Thick-Light[https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=39030]</ref>. The content is to remain accurate as such.}}
 ==Step1==
-gram of ACRB, freeze/thaw twice
+Place 500 gram of ACRB in container and freeze/thaw twice.
 ==Step2==
-Boil in 2000ml of water with 100ml white vinegar for 1.5 hrs, then transfer liquid to another pot and start reducing it
+Boil ACRB in 2000ml of water with 100ml white vinegar for 1.5 hrs, then transfer liquid to another pot and start reducing it.
 ==Step3==
-repeat step2 at least 4 times, adding fresh vinegar each time
+Repeat '''Step2''' at least 4 times, adding 100ml fresh vinegar each time.
 ==Step4==
-reduce total liquid volume to around 1500ml, then let cool and pour into your extraction vessel. (A half gallon mason jar works well).
+Reduce total liquid volume to around 1500ml, then let cool and pour into your extraction vessel. (A half gallon mason jar works well).
 ==Step5==
-Slowly add 150g of NaOh and stir.
+Slowly add 150g of NaOh and stir. Be '''careful''' when adding NaOh, as the reaction can cause bubbling.
 ==Step6==
 While the liquid is still warm, add 600ml of naptha, cap the extraction vessel, and with gloves and goggles on, shake it over a sink vigourously. Do this 6-10 times, letting the naptha and soup completely separate between agitation. On your last shake, roll the naptha around the jar lightly to reduce emulsions.
@@ Line 20: / Line 20: @@
 The solvent you poured off should be put in a freezer for 24-48 hours so all the goodies can be freeze precipitated. Once this happens, pour the solvent off then back into the basified ACRB soup. Scrape the crystals from the jar once they are dry.
 ==Step10==
- repeat shaking the jar with the naptha and a. confusa soup 6-10 times letting it seperate then shake it again etc... If the solvent is still cloudy white let it sit 6-8 hours and the saturated dmt should crystalize inside the solvent. If it doesn't then it's not saturated enough.
+Repeat shaking the jar with the naptha and [[Acacia confusa]] soup 6-10 times letting it seperate then shake it again etc... If the solvent is still cloudy white let it sit 6-8 hours and the saturated dmt should crystalize inside the solvent. If it doesn't then it's not saturated enough.
 If that's the case let the naptha evap half way then stick it in the freezer and let it freeze precipitate. 24-48 hors. at this point pour off the solvent and let the crystals dry then scape them up wait til the naptha smell is gone and enjoy!!!!
@@ Line 26: / Line 26: @@
 ==Additional notes/tips:::==
-* Keep the jar in a heat bath the whole time you are doing pulls that way the naptha will stay warm and stay saturated until you decant it. plug the sink run hot water add a kettle of boiling water every 15-20 minutes or when it starts getting cool.
+* Keep the jar in a heat bath the whole time you are doing pulls, that way the naptha will stay warm and stay saturated until you decant it. Plug the sink, run hot water; add a kettle of boiling water every 15-20 minutes or when it starts getting cool.
-*  filtering the final boils before basing results in a less than likely chance of ending up with dirty naptha...
+* Filtering the final boils before basing, results in a less than likely chance of ending up with dirty Naptha.
-* I have done up to ten pulls and got spice on every single one. If you don't take the time to shake and let the nps separate at least 6 times on your first pull it may not contain enough spice to allow room temp crystallization in the solvent. In experiments the 2nd and 3rd pull sometimes drop more crystals when freeze precipitated if the first pull is only allowed to mix and sep. 3 times. Generally the later pulls produce a sandy colored powder with beige crystals. Upon re-x this sandy powder produces a chalky pure white powder and a tan goo that dries to a peachy tan. I assume it's nmt but i'm not sure. Some should be sent out for a alk profile so we know for sure what it is.
+* If you don't take the time to shake and let the non-polar solvent (naptha) separate at least 6 times on your first pull, it may not contain enough spice to allow room temp crystallization in the solvent. Generally the later pulls produce a sandy colored powder with beige crystals. Upon re-x this sandy powder produces a chalky pure white powder and a tan goo that dries to a peachy tan.
-* I also boiled the root bark first then froze it boiled it again then froze again, then while it was soft from the second boil I used a blender to shred it up almost to powder. I'm not sure if the freezing is essential but it helps to break the bark apart as the water expands and cracks the bark.
+* I also boiled the root bark first, then froze it, boiled it again, then froze again. Then while it was soft from the second boil, I used a blender to shred it up almost to powder. I'm not sure if the freezing is essential but it helps to break the bark apart as the water expands and cracks the bark.
-* No vodka powder or vinegar when i was freezing it. I actually soaked it in water then poured it off in the pot I was using for the boils then froze and thawed it 2x before cooking.
+* No vodka powder or vinegar when freezing it. Soak it in water then poured it off in the pot for the boils, then freeze and thaw it 2x before cooking.
-* didn't powder my bark due to the pains of filtering all the sediment as your doing consecutive boils.
+* Don't powder my bark due to the pains of filtering all the sediment as you're doing consecutive boils.