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2C-T-17

Field	Value
Verifiedfields	changed
Watchedfields	changed
verifiedrevid	477216604
image	2C-T-17 2DACS.svg
image_class	skin-invert-image
width	250px
image2	2C-T-17-3d-sticks.png
image_class2	bg-transparent
width2	250px
routes_of_administration	Oral
class	Serotonergic psychedelic; Hallucinogen
ATC_prefix	None
duration_of_action	10–15 hours
CAS_number_Ref
CAS_number	207740-32-7
PubChem	44349798
ChemSpiderID_Ref
ChemSpiderID	21106230
UNII	NLC3VH4KZM
ChEMBL_Ref
ChEMBL	127284
synonyms	4-sec-Butylthio-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-sec-butylthiophenethylamine; NIMITZ; Nimitz
IUPAC_name	2-(4-butan-2-ylsulfanyl-2,5-dimethoxyphenyl)ethanamine
C	14	H=23	N=1	O=2	S=1
SMILES	CC(CC)Sc1cc(OC)c(cc1OC)CCN
StdInChI_Ref
StdInChI	1S/C14H23NO2S/c1-5-10(2)18-14-9-12(16-3)11(6-7-15)8-13(14)17-4/h8-10H,5-7,15H2,1-4H3
StdInChIKey_Ref
StdInChIKey	KSZHVRPGICAZOA-UHFFFAOYSA-N

| Drugs.com =

| elimination_half-life =

2C-T-17, also known as 4-sec-butylthio-2,5-dimethoxyphenethylamine or as Nimitz, is a psychedelic drug of the phenethylamine and 2C families. It is taken orally.

2C-T-17 was first described in the scientific literature by Alexander Shulgin and colleagues in 1991. Shortly after this, Shulgin described 2C-T-17 in greater detail in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).

Use and effects

According to Alexander Shulgin in his book PiHKAL (Phenethylamines I Have Known and Loved), 2C-T-17's dose range is 60 to 100mg and its duration is 10 to 15hours. Its onset is 1hour and peak effects occurred after 3hours. 2C-T-17 has been described as a "truly heavy psychedelic" but as producing no psychedelic visuals and very little in the way of perceptual changes. User reports described it as having pronounced psychoactive effects but had difficulty describing exactly what those effects were.

Toxicity

The toxicity of 2C-T-17 is not well-documented. It 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 of action that produces 2C-T-17's hallucinogenic effects has not been specifically established, however it is most likely to result from action as a serotonin 5-HT2A 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-17 is the 2 carbon homologue of Aleph-17, which has never been synthesized. The full chemical name is 2-4-(2-[butyl thio)-2,5-dimethoxy phenyl]ethanamine. The drug has structural properties similar to drugs in the 2C-T series, with the most closely related compounds being 2C-T-7 and 2C-T-8.

History

2C-T-17 was first described in the scientific literature by Alexander Shulgin and colleagues in a journal article in 1991. Shortly thereafter, it was described in greater detail by Shulgin in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).

Society and culture

Legal status

Canada

As of October 31, 2016, 2C-T-17 is a controlled substance (Schedule III) in Canada.

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.

United States

2C-T-17 is not illegal, but possession and sales of 2C-T-17 could be prosecuted under the Federal Analog Act in the United States 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)".
"UK Misuse of Drugs act 2001 Amendment summary". Isomer Design.

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) pihkal psychedelic-phenethylamines sec-butyl-compounds thioethers

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