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2C-T-15

Field	Value
Verifiedfields	changed
Watchedfields	changed
verifiedrevid	477216583
image	2C-T-15 2DACS.svg
image_class	skin-invert-image
width	225px
image2	2C-T-15-3d-sticks.png
image_class2	bg-transparent
width2	250px
routes_of_administration	Oral
class	Serotonergic psychedelic; Hallucinogen
ATC_prefix	None
duration_of_action	"Several hours"
CAS_number_Ref
CAS_number	952006-95-0
PubChem	44719534
ChemSpiderID_Ref
ChemSpiderID	21106229
UNII	4DC109467K
synonyms	4-Cyclopropylthio-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-cyclopropylthiophenethylamine; SESQUI
IUPAC_name	2-[4-(cyclopropylsulfanyl)-2,5-dimethoxyphenyl]ethan-1-amine
C	13	H=19	N=1	O=2	S=1
SMILES	COc2cc(SC1CC1)c(cc2CCN)OC
StdInChI_Ref
StdInChI	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
StdInChIKey_Ref
StdInChIKey	HHAPMOUVSYQKLK-UHFFFAOYSA-N
melting_point	203.5
melting_high	204.5

| Drugs.com =

| elimination_half-life =

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

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." 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.

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.

Chemistry

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

History

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

Society and culture

Legal status

Canada

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

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.

References

{{CitePiHKAL
(January 1991). "Central nervous system (CNS) activity of two new psychoactive compounds". Journal of Psychoactive Drugs.
(4 May 2016). "Canada Gazette – Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)".

Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

2c-(psychedelics) cyclopropyl-compounds pihkal thioethers

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