2C-T-15

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2C-T-15
Chemical name 2-[4-(cyclopropylthio)-2,5-dimethoxyphenyl]ethanamine
Chemical formula C13H19NO2S
CAS number ?
Molecular mass 253.36 g/mol
Melting point 203.5-204.5 °C
Amphetamine analog Aleph-15 (not synthesized)
Chemical structure of 2C-T-15
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2C-T-15 or 2,5-dimethoxy-4-(β-cyclopropylthio)phenethylamine is a psychedelic phenethylamine of the 2C family. It was presumably first synthesized by Alexander Shulgin and reported in his book PIHKAL.

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.

General Information

The dosage 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."[1] The effects are not prominent, and 2C-T-15 is not very potent.

Pharmacology

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.

Dangers

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. Other phenethylamine derivatives substituted with an alkylthio group at the 4 position such as 2C-T-7 and 4-MTA are known to act as selective monoamine oxidase A inhibitors, a side effect which can lead to lethal serotonin syndrome when they are combined with stimulant drugs. Most confirmed fatalities involving 2C-T drugs involve their combination with other hard drugs such as alcohol, ecstasy or cocaine.

Legality

2C-T-15 is not illegal, 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.

Reference

  1. Shulgin, Alexander (1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. Unknown parameter |month= ignored (help); Unknown parameter |coauthors= ignored (help)

Categorization

External links


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