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2C-T: Difference between revisions
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2C-T was first synthesized as part of a collaboration between researchers [[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 was first synthesized as part of a collaboration between researchers [[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> | ||
Its effects and synthesis is described in Shulgin's 1991 book [[PiHKAL]] ("Phenethylamines I Have Known and Loved").<ref name="pihkal2CT">Shulgin, A., & Shulgin, A. (1991).</ref> | Its effects and synthesis is described in Shulgin's 1991 book [[PiHKAL]] ("Phenethylamines I Have Known and Loved").<ref name="pihkal2CT">Shulgin, A., & Shulgin, A. (1991).</ref> | ||
2C-T's subjective effects are not well-characterized. Preliminary anecdotal reports appear to indicate it has some of the psychedelic effects of [[2C-T-2]] and [[2C-T-7]]. The effects of 2C-T have been described as being less visual and more tactile. | |||
Very little data exists about the pharmacological properties, metabolism, and toxicity of 2C-T, and it has a relatively short history of human usage. It is highly advised to use [[harm reduction practices]] if using this substance. | Very little data exists about the pharmacological properties, metabolism, and toxicity of 2C-T, and it has a relatively short history of human usage. It is highly advised to use [[harm reduction practices]] if using this substance. | ||
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==Chemistry== | ==Chemistry== | ||
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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The effects of 2C-T have been described as being less visual and more in the body. | The effects of 2C-T have been described as being less visual and more in the body. | ||
{{Preamble/SubjectiveEffects}} | {{Preamble/SubjectiveEffects}} | ||
{{effects/base | {{effects/base | ||