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2C-T
Names
	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
CAS Number	61638-09-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL127252 ;
ChemSpider	10438674 ;
ECHA InfoCard	100.215.648
PubChem CID	12315927;
UNII	E5X0VFF7S4 ;
CompTox Dashboard (EPA)	DTXSID60487530 ;
	InChI InChI=1S/C11H17NO2S/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12/h6-7H,4-5,12H2,1-3H3 Key: UPZMYCMLLQTYEM-UHFFFAOYSA-N ; InChI=1/C11H17NO2S/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12/h6-7H,4-5,12H2,1-3H3 Key: UPZMYCMLLQTYEM-UHFFFAOYAU;
	SMILES CSc1cc(OC)c(cc1OC)CCN;
Properties
Chemical formula	C11H17NO2S
Molar mass	227.32 g/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302
Precautionary statements	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). verify (what is ?) Infobox references

2C-T (or 4-methylthio-2,5-DMPEA) is a psychedelic and hallucinogenic drug of the 2C family. It is used by some as an entheogen. It has structural and pharmacodynamic properties similar to the drugs mescaline and 2C-T-2.

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 phenethylamines, and is the 4-methyl thio analogue of 2C-O, a positional isomer of mescaline. It is also the 2C analog of Aleph. The systematic name of the chemical is 2-(2,5-dimethoxy-4-(methyl thio)phenyl)ethanamine. The CAS number of 2C-T is 61638-09-3.

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-HT_2A 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 United States; however its close similarity in structure and effects to 2C-T-7 could potentially subject possession and sale of 2C-T to prosecution under the Federal Analog Act. This seems to be the tack the federal government is taking in the wake of the DEA's Operation Web Tryp. A series of court cases in the US involving the prosecution of several online vendors were commenced in 2004 and resulted in a number of convictions.^[4]