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2C-T-15

From Wikipedia, the free encyclopedia

Pharmaceutical compound
2C-T-15
Clinical data
Other names4-Cyclopropylthio-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-cyclopropylthiophenethylamine; SESQUI
Routes of
administration
Oral[1]
Drug classSerotonergic 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
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H19NO2S
Molar mass253.36 g·mol−1
3D model (JSmol)
Melting point203.5 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 checkY
  • Key:HHAPMOUVSYQKLK-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2C-T-15, also known as4-cyclopropylthio-2,5-dimethoxyphenethylamine, is apsychedelicphenethylamine of the2C family.[1] It was presumably first synthesized byAlexander Shulgin and reported in his bookPiHKAL (Phenethylamines i Have Known And Loved).[1]

Use and effects

[edit]

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

Toxicity

[edit]

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

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

[edit]

Pharmacodynamics

[edit]

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 a5-HT2Aserotonin receptoragonist 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

[edit]

2C-T-15 is the2 carbonhomologue ofAleph-15, which has not been synthesized.[1] The full chemical name is 2-[4-(2-cyclopropylthio)-2,5-dimethoxyphenyl]ethanamine.[1] The drug hasstructural properties similar to2C-T-2 and other drugs in the2C-T series.[1]

History

[edit]

2C-T-15 was first described in thescientific literature byAlexander Shulgin and colleagues in 1991.[2]

Society and culture

[edit]

Legal status

[edit]

Canada

[edit]

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

United Kingdom

[edit]

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

United States

[edit]

2C-T-15 is not explicitly illegal in the USA, but possession and sales of 2C-T-15 could be prosecuted under theFederal Analog Act because of its structural similarities to2C-T-7.

See also

[edit]

References

[edit]
  1. ^abcdefghShulgin 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 fromthe original on 2025-07-13.
  3. ^"Canada Gazette – Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)". 4 May 2016.

External links

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