2C-T
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| Names | |
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| Preferred IUPAC name
2-[2,5-Dimethoxy-4-(methylsulfanyl)phenyl]ethan-1-amine | |
| Other names
2-[2,5-Dimethoxy-4-(methylthio)phenyl]ethan-1-amine
2-[2,5-Dimethoxy-4-(methylthio)phenyl]ethanamine | |
| Identifiers | |
3D model (
JSmol ) |
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| ChEMBL | |
| ChemSpider | |
ECHA InfoCard
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100.215.648 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C11H17NO2S | |
| Molar mass | 227.32 g/mol |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H302 | |
| P264, P270, P301+P312, P330, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2C-T (or 4-methylthio-2,5-DMPEA) is a
It was first synthesized and studied through a collaboration between David E. Nichols and Alexander Shulgin.[1]
Chemistry
2C-T is in a class of compounds commonly known as
Effects
2C-T's active dosage is around 75–150 mg and produces mescaline and MDMA-like effects that may last up to 6 hours.[2]
Pharmacology
The mechanism that produces 2C-T’s hallucinogenic and entheogenic effects has not been specifically established, however it is most likely to result from action as a 5-HT2A serotonin receptor agonist in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines for which the mechanism of action is known.
Popularity
2C-T is almost unknown on the black market although it has rarely been sold by "research chemical" companies. Limited accounts of 2C-T can be found in the book PiHKAL.[2]
Legality
Canada
As of October 31, 2016; 2C-T is a controlled substance (Schedule III) in Canada.[3]
United States
2C-T is unscheduled and unregulated in the