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		<id>https://wiki.dmt-nexus.me/w/index.php?action=history&amp;feed=atom&amp;title=Psilocin_%26_Psilocybin</id>
		<title>Psilocin &amp; Psilocybin - Revision history</title>
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		<updated>2026-05-10T12:38:16Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wiki.dmt-nexus.me/w/index.php?title=Psilocin_%26_Psilocybin&amp;diff=5737&amp;oldid=prev</id>
		<title>TheTraveler: Text replace - &quot;dmt-nexus.com&quot; to &quot;dmt-nexus.me&quot;</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/w/index.php?title=Psilocin_%26_Psilocybin&amp;diff=5737&amp;oldid=prev"/>
				<updated>2012-01-31T19:56:49Z</updated>
		
		<summary type="html">&lt;p&gt;Text replace - &amp;quot;dmt-nexus.com&amp;quot; to &amp;quot;dmt-nexus.me&amp;quot;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
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				&lt;tr style='vertical-align: top;'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Revision as of 19:56, 31 January 2012&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 16:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 16:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Stability/Degradation: Unstable in solution, especially alkaline solution (Merck Index).&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Stability/Degradation: Unstable in solution, especially alkaline solution (Merck Index).&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Solubility:&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Solubility:&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&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.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&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.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;me&lt;/ins&gt;/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;me&lt;/ins&gt;/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;=== Psilocybin ===&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;=== Psilocybin ===&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 26:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 26:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Composition: C12H17N2O4P&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Composition: C12H17N2O4P&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Molecular Weight: 284.248141 g/mol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Molecular Weight: 284.248141 g/mol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Melting Point: 220-228° from boiling water; 185-195° from boiling methanol ([http://wiki.dmt-nexus.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/w/images/8/81/MERCK.pdf Merck Index])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Melting Point: 220-228° from boiling water; 185-195° from boiling methanol ([http://wiki.dmt-nexus.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;me&lt;/ins&gt;/w/images/8/81/MERCK.pdf Merck Index])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* XLogP3: -1.6 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=10624&amp;amp;loc=ec_rcs PubChem])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* XLogP3: -1.6 ([http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=10624&amp;amp;loc=ec_rcs PubChem])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Colorimetric reagent results: [https://www.dmt-nexus.me/forum/default.aspx?g=posts&amp;amp;t=25771 Here]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Stability/Degradation: Dephosphorylated into Psilocin under acidic conditions. Also when ingested, by phosphatases enzymes.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Stability/Degradation: Dephosphorylated into Psilocin under acidic conditions. Also when ingested, by phosphatases enzymes.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Solubility:&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;* Solubility:&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&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.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&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.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;me&lt;/ins&gt;/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;me&lt;/ins&gt;/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Effects ==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Effects ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>TheTraveler</name></author>	</entry>

	<entry>
		<id>https://wiki.dmt-nexus.me/w/index.php?title=Psilocin_%26_Psilocybin&amp;diff=4936&amp;oldid=prev</id>
		<title>Endlessness: Created page with &quot;== Brief overview - What is Bufotenine? ==  == Chemical and physical properties ==  === Psilocin === 4-HO-DMT - 4-Hydroxy-N,N-dimethyl-tryptamine  ==== Freebase Psilocin ==== &lt;ta...&quot;</title>
		<link rel="alternate" type="text/html" href="https://wiki.dmt-nexus.me/w/index.php?title=Psilocin_%26_Psilocybin&amp;diff=4936&amp;oldid=prev"/>
				<updated>2011-11-07T11:59:24Z</updated>
		
		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Brief overview - What is Bufotenine? ==  == Chemical and physical properties ==  === Psilocin === 4-HO-DMT - 4-Hydroxy-N,N-dimethyl-tryptamine  ==== Freebase Psilocin ==== &amp;lt;ta...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Brief overview - What is Bufotenine? ==&lt;br /&gt;
&lt;br /&gt;
== Chemical and physical properties ==&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.com/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.com/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.com/w/images/8/81/MERCK.pdf Merck Index])&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.com/w/images/8/81/MERCK.pdf Merck Index] , [https://www.dmt-nexus.com/forum/default.aspx?g=posts&amp;amp;m=221711#post221711 scientific publications])&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
&lt;br /&gt;
== Pharmacology, toxicity and general safety ==&lt;br /&gt;
&lt;br /&gt;
== Plants containing bufotenine ==&lt;br /&gt;
&lt;br /&gt;
== Extraction teks ==&lt;br /&gt;
&lt;br /&gt;
== Dosages and consumption methods ==&lt;br /&gt;
&lt;br /&gt;
== History of usage ==&lt;br /&gt;
&lt;br /&gt;
== Analysis of bufotenine ==&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>Endlessness</name></author>	</entry>

	</feed>