2C-T-13

2C-T-13

Names
Preferred IUPAC name 2-{2,5-Dimethoxy-4-[(2-methoxyethyl)sulfanyl]phenyl}ethan-1-amine
Identifiers
CAS Number	207740-30-5 N
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL123868 Y
ChemSpider	21106228 Y
PubChem CID	44350108
UNII	SK8JCS3S9B N
CompTox Dashboard (EPA)	DTXSID10658379
InChI InChI=1S/C13H21NO3S/c1-15-6-7-18-13-9-11(16-2)10(4-5-14)8-12(13)17-3/h8-9H,4-7,14H2,1-3H3 Y Key: PYJLRNOGMKMRTK-UHFFFAOYSA-N Y InChI=1/C13H21NO3S/c1-15-6-7-18-13-9-11(16-2)10(4-5-14)8-12(13)17-3/h8-9H,4-7,14H2,1-3H3 Key: PYJLRNOGMKMRTK-UHFFFAOYAS
SMILES COc1cc(SCCOC)c(cc1CCN)OC
Properties
Chemical formula	C13H21NO3S
Molar mass	271.38 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

2C-T-13 (2,5-dimethoxy-4-(β-methoxyethylthio)phenethylamine) is a psychedelic phenethylamine of the 2C family. It was presumably first synthesized by Alexander Shulgin and reported in his book PiHKAL.^[1]

The drug has structural properties similar to mescaline and other drugs in the 2C-T series, with the most closely related compounds being 2C-T-7 and 2C-T-21.

The dosage range of 2C-T-13 is typically 25 - 40 mg and its duration is approximately 6–8 hours according to Shulgin.^[1] 2C-T-13 produces many closed-eye visuals and geometric patterns. It also produces slight visual distortion.^[1]

This section needs more reliable medical references for verification or relies too heavily on primary sources. Please review the contents of the section and add the appropriate references if you can. Unsourced or poorly sourced material may be challenged and removed. Find sources: "2C-T-13" – news · newspapers · books · scholar · JSTOR (July 2019)

The mechanism that produces 2C-T-13'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.

The toxicity of 2C-T-13 is not well documented. 2C-T-13 is slightly less potent than 2C-T-7, but it may be expected that at higher doses it would display similar toxicity to that of other phenethylamines of the 2C-T family.

2C-T-13 is not scheduled in the United States, but possession and sales of 2C-T-13 could be prosecuted under the Federal Analog Act because of its structural similarities to 2C-T-7.

As of October 31, 2016, 2C-T-13 is a controlled substance (Schedule III) in Canada.^[2]