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2C-T: Difference between revisions
>Tracer Discussion on Bluelight and Erowid experience vaults |
>Mydriasis Updated effects, visual. Also grammar. |
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It is a member of the [[2C-x family]] of psychedelic phenethylamines, all of which were derived from the systematic modification of the [[mescaline]] molecule. | It is a member of the [[2C-x family]] of psychedelic phenethylamines, all of which were derived from the systematic modification of the [[mescaline]] molecule. | ||
2C-T It was first synthesized and studied through a collaboration between [[David E. Nichols]] and [[Alexander Shulgin]]<ref>Nichols DE, Shulgin AT (October 1976). "Sulfur analogs of psychotomimetic amines". J Pharm Sci. 65 (10): 1554–6. CiteSeerX 10.1.1.687.8486. doi:10.1002/jps.2600651040. PMID 978423.</ref> | 2C-T It was first synthesized and studied through a collaboration between [[David E. Nichols]] and [[Alexander Shulgin]].<ref>Nichols DE, Shulgin AT (October 1976). "Sulfur analogs of psychotomimetic amines". J Pharm Sci. 65 (10): 1554–6. CiteSeerX 10.1.1.687.8486. doi:10.1002/jps.2600651040. PMID 978423.</ref> | ||
It is described in Shulgin's 1991 book [[PiHKAL]] ("Phenethylamines I Have Known and Loved").<ref name="pihkal2CT">Shulgin, A., & Shulgin, A. (1991).</ref> | It is described in Shulgin's 1991 book [[PiHKAL]] ("Phenethylamines I Have Known and Loved").<ref name="pihkal2CT">Shulgin, A., & Shulgin, A. (1991).</ref> | ||
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==Chemistry== | ==Chemistry== | ||
[[File: | [[File:Phenethylamine.png|thumb|right|250px|thumb|right|250px||Generic structure of a phenethylamine molecule]] | ||
2C-T, or 2,5-dimethoxy-4-methylthiophenethylamine, is a substituted [[phenethylamines|phenethylamine]] featuring a phenyl ring bound to an amino (NH<sub>2</sub>) group through a methyl chain. 2C-T belongs to the 2C family of phenethylamines which contain methoxy functional groups CH<sub>3</sub>O- attached to carbons R<sub>2</sub> and R<sub>5</sub> of the benzene ring. 2C-T is also substituted at R<sub>4</sub> with an methyl thioether group. | 2C-T, or 2,5-dimethoxy-4-methylthiophenethylamine, is a substituted [[phenethylamines|phenethylamine]] featuring a phenyl ring bound to an amino (NH<sub>2</sub>) group through a methyl chain. 2C-T belongs to the 2C family of phenethylamines which contain methoxy functional groups CH<sub>3</sub>O- attached to carbons R<sub>2</sub> and R<sub>5</sub> of the benzene ring. 2C-T is also substituted at R<sub>4</sub> with an methyl thioether group. | ||
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However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive. | However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive. | ||
Being similar in structure to | Being similar in structure to 2C-T-2 and 2C-T-7, this compound may have some MAOI properties. | ||
==Subjective effects== | ==Subjective effects== | ||
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{{effects/base | {{effects/base | ||
|{{effects/physical| | |{{effects/physical| | ||
*'''[[Effect::Spontaneous physical sensations]] | *'''[[Effect::Spontaneous physical sensations]]'' | ||
*'''[[Effect::Bodily control enhancement]]''' | *'''[[Effect::Bodily control enhancement]]''' | ||
*'''[[Effect::Tactile enhancement]]''' "Tactile sensitivity" | *'''[[Effect::Tactile enhancement]]''' "Tactile sensitivity" | ||
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}} | }} | ||
{{effects/visual| | {{effects/visual| | ||
The visual component of this substance is reported to be minimal even at higher doses. | |||
====Enhancements==== | ====Enhancements==== | ||
*'''[[Effect::Visual acuity enhancement]]''' | *'''[[Effect::Visual acuity enhancement]]''' | ||
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====Distortions==== | ====Distortions==== | ||
*'''[[Effect::Drifting]]''' ''([[Drifting#Melting|melting]], [[Drifting#Flowing|flowing]], [[Drifting#Breathing|breathing]] and [[Drifting# morphing|morphing]])'' | *'''[[Effect::Drifting]]''' ''([[Drifting#Melting|melting]], [[Drifting#Flowing|flowing]], [[Drifting#Breathing|breathing]] and [[Drifting# morphing|morphing]])'' | ||
*'''[[Effect::Tracers]]''' | *'''[[Effect::Tracers]]''' | ||
*'''[[Effect::After images]]''' | *'''[[Effect::After images]]''' | ||
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}} | }} | ||
|{{effects/cognitive| | |{{effects/cognitive| | ||
The head space of 2C-T is described | The head space of 2C-T is described as both insightful and relatively normal in its thought processes even at moderate to high doses. | ||
*'''[[Effect::Emotion enhancement]]''' | *'''[[Effect::Emotion enhancement]]''' | ||
*'''[[Effect::Novelty enhancement]]''' | *'''[[Effect::Novelty enhancement]]''' | ||
*'''[[Effect::Time distortion]]''' | *'''[[Effect::Time distortion]]''' | ||
*'''[[Effect::Analysis enhancement]]''' | *'''[[Effect::Analysis enhancement]]''' | ||
*'''[[Effect::Personal bias suppression]]''' | *'''[[Effect::Personal bias suppression]]''' | ||
*'''[[Effect::Conceptual thinking]]''' | *'''[[Effect::Conceptual thinking]]''' | ||
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===Experience reports=== | ===Experience reports=== | ||
There are currently no anecdotal reports which describe the effects of this compound within our [[experience index]]. | There are currently no anecdotal reports which describe the effects of this compound within our [[experience index]]. | ||
==Toxicity and harm potential== | ==Toxicity and harm potential== | ||
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*[https://en.wikipedia.org/wiki/2C-T 2C-T (Wikipedia)] | *[https://en.wikipedia.org/wiki/2C-T 2C-T (Wikipedia)] | ||
*[https://isomerdesign.com/PiHKAL/read.php?domain=pk&id=39 2C-T (PiHKAL / Isomer Design)] | *[https://isomerdesign.com/PiHKAL/read.php?domain=pk&id=39 2C-T (PiHKAL / Isomer Design)] | ||
===Discussion=== | ===Discussion=== | ||
==References== | ==References== | ||