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2C-T-17





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2C-T-17or2,5-dimethoxy-4-(β-secbutylthio)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).

2C-T-17
Names
Preferred IUPAC name

2-{4-[(Butan-2-yl)sulfanyl]-2,5-dimethoxyphenyl}ethan-1-amine

Identifiers

CAS Number

3D model (JSmol)

ChEMBL
ChemSpider

PubChem CID

UNII

CompTox Dashboard (EPA)

  • 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 checkY

    Key: KSZHVRPGICAZOA-UHFFFAOYSA-N checkY

  • 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

  • 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).

☒N verify (what is checkY☒N ?)

Infobox references

Chemistry

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2C-T-17 is the 2 carbon homologueofAleph-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

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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

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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-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.

Dangers

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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

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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

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

United Kingdom

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

References

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  1. ^ Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
  • ^ "Canada Gazette – Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)". 4 May 2016.
  • ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.
  • edit

    Retrieved from "https://en.wikipedia.org/w/index.php?title=2C-T-17&oldid=1190747547"
     



    Last edited on 19 December 2023, at 16:33  





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    This page was last edited on 19 December 2023, at 16:33 (UTC).

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