Assessment |
Biopsychology |
Comparative |
Cognitive |
Developmental |
Language |
Individual differences |
Personality |
Philosophy |
Social |
Methods |
Statistics |
Clinical |
Educational |
Industrial |
Professional items |
World psychology |
Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
2C-T-9 | |
---|---|
Chemical name | 2-[4-(butylthio)-2,5-dimethoxyphenyl]ethanamine |
Chemical formula | C14H23NO2S |
CAS number | 207740-28-1 |
Molecular mass | 269.403 g/mol |
Melting point | ? |
|
2C-T-9 is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin, sometimes used as an entheogen.
Chemistry[]
2C-T-9 is 2,5-dimethoxy-4-(n)-butylthiophenethylamine.
The IUPAC name of 2C-T-9 is 1-(4-(n-butylthio)-2,5-dimethoxyphenyl)-2-aminoethane.
Dosage[]
In his book PIHKAL (Phenethylamines I Have Known and Loved), Shulgin lists the dosage range as 60 - 100 mg.
Subjective Qualities[]
It is generally taken orally, and effects typically last 12 to 18 hours. There have been no reported deaths from 2C-T-9. The drug is said to taste like motor oil, and experiences have focused primarily on energy as opposed to creativity or insight.
Pharmacology[]
The mechanism that produces 2C-T-9’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-9 is not well documented. 2C-T-9 is considerably less potent than 2C-T-7, but it may be expected that at higher 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-9 is not illegal, but possession and sales of 2C-T-9 could be prosecuted under the Federal Analog Act because of its structural similarities to 2C-T-7.
External links[]
Psychedelic phenethylamines
| |
---|---|
Aleph • 2C-B • 2C-B-FLY • 2C-C • 2C-D • 2C-E • 2C-F • 2C-G • 2C-I • 2C-N • 2C-O • 2C-O-4 • 2C-P • 2C-T • 2C-T-2 • 2C-T-4 • 2C-T-7 • 2C-T-8 • 2C-T-9 • 2C-T-13 • 2C-T-15 • 2C-T-17 • 2C-T-21 • 2C-TFM • 3C-E • 3C-P • Br-DFLY • DESOXY • DMMDA-2 • DOB • DOC • DOET • DOI • DOM • DON • Escaline • Ganesha • HOT-2 • HOT-7 • HOT-17 • Isoproscaline • Lophophine • MDA • MMDA • MMDA-2 • MMDA-3a • MMDMA • Macromerine • Mescaline • Proscaline • TMA |
.
This page uses Creative Commons Licensed content from Wikipedia (view authors). |