2C-T-17

2C-T-17
Names
	IUPAC name 2-[4-(but-2-ylthio)-2,5-dimethoxyphenyl]ethanamine
Identifiers
CAS Number	207740-32-7 [chemspider];
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL127284 ;
ChemSpider	21106230 ;
PubChem CID	44349798;
UNII	NLC3VH4KZM;
CompTox Dashboard (EPA)	DTXSID20658365 ;
	InChI InChI=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 Key: KSZHVRPGICAZOA-UHFFFAOYSA-N ; InChI=1/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 Key: KSZHVRPGICAZOA-UHFFFAOYAV;
	SMILES CC(CC)Sc1cc(OC)c(cc1OC)CCN;
Properties
Chemical formula	C14H21NO2S
Molar mass	269.40 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

2C-T-17 or 2,5-dimethoxy-4-(β-secbutyl thio)phenethylamine 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).

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.

General information

The dosage range of 2C-T-17 is typically 60-100 mg and its duration is approximately 10–15 hours according to Shulgin. 2C-T-17 has highly psychedelic effects on thinking, but produces few to no visuals.[1]

Pharmacology

The mechanism that produces 2C-T-17'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.

Dangers

The toxicity of 2C-T-17 is not well documented. 2C-T-17 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.

Legality

2C-T-17 is not illegal, but possession and sales of 2C-T-17 could be prosecuted under the Federal Analog Act because of its structural similarities to 2C-T-7.

Canada

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

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[3]

gollark: I mean, they aren't very practical, but you *could*, if you wanted to, ride places by pig.

gollark: Via kinetic augment.

gollark: We did make pigs fly a few times.

gollark: Anyway, that isn't an inductive proof, thus I am right in all cases.

gollark: Can you *not* just terminate it?

References

Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
http://gazette.gc.ca/rp-pr/p2/2016/2016-05-04/html/sor-dors72-eng.php
"UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.

External links

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

[2] ttp://gazette.gc.ca/rp-pr/p2/2016/2016-05-04/html/sor-dors72-eng.php

[3] "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.