2C-T-15

Last updated

2C-T-15
2C-T-15 2DACS.svg
2C-T-15-3d-sticks.png
Clinical data
Other names4-Cyclopropylthio-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-cyclopropylthiophenethylamine; SESQUI
Routes of
administration 		Oral [1]
Drug class Serotonergic psychedelic; Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action "Several hours" [1]
Identifiers
  • 2-[4-(cyclopropylsulfanyl)-2,5-dimethoxyphenyl]ethan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
Formula C13H19NO2S
Molar mass 253.36 g·mol−1
3D model (JSmol)
Melting point 203.5 to 204.5 °C (398.3 to 400.1 °F)
  • COc2cc(SC1CC1)c(cc2CCN)OC
  • InChI=1S/C13H19NO2S/c1-15-11-8-13(17-10-3-4-10)12(16-2)7-9(11)5-6-14/h7-8,10H,3-6,14H2,1-2H3 Yes check.svgY
  • Key:HHAPMOUVSYQKLK-UHFFFAOYSA-N Yes check.svgY
 X mark.svgNYes check.svgY  (what is this?)    (verify)

2C-T-15, also known as 4-cyclopropylthio-2,5-dimethoxyphenethylamine, is a psychedelic phenethylamine of the 2C family. [1] It was presumably first synthesized by Alexander Shulgin and reported in his book PiHKAL (Phenethylamines i Have Known And Loved) . [1]

Contents

Use and effects

The dose range of 2C-T-15 is typically 30 mg or more. Its duration is unspecified by Shulgin, and its entry in PiHKAL says it lasts for "several hours." [1] The effects are not prominent, and 2C-T-15 is not very potent.

Toxicity

The toxicity of 2C-T-15 is not well documented. 2C-T-15 is much less potent than 2C-T-7, but it may be expected that at very high doses it would display similar toxicity to that of other phenethylamines of the 2C-T family.[ citation needed ]

Interactions

Pharmacology

Pharmacodynamics

The mechanism that produces 2C-T-15'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.[ citation needed ]

Chemistry

2C-T-15 is the 2 carbon homologue of Aleph-15, which has not been synthesized. [1] The full chemical name is 2-[4-(2-cyclopropyl thio)-2,5-dimethoxy phenyl]ethanamine. [1] The drug has structural properties similar to 2C-T-2 and other drugs in the 2C-T series. [1]

History

2C-T-15 was first described in the scientific literature by Alexander Shulgin and colleagues in 1991. [2]

Society and culture

Canada

As of October 31, 2016, 2C-T-15 is a controlled substance (Schedule III) in Canada. [3]

United Kingdom

2C-T-15 is a class A drug in the UK under the Misuse of Drugs act.

United States

2C-T-15 is not explicitly illegal in the USA, but possession and sales of 2C-T-15 could be prosecuted under the Federal Analog Act because of its structural similarities to 2C-T-7.

See also

References

  1. 1 2 3 4 5 6 7 8 Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN   0-9630096-0-5. OCLC   25627628.
  2. ↑ Shulgin AT, Shulgin A, Jacob P (January 1991). "Central nervous system (CNS) activity of two new psychoactive compounds". Journal of Psychoactive Drugs. 23 (1): 95–96. doi:10.1080/02791072.1991.10472583. eISSN   2159-9777. PMID   1941371. Archived from the original on 2025-07-13.
  3. ↑ "Canada Gazette – Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)". 4 May 2016.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.