2C-T-9
From Wikipedia, the free encyclopedia
2C-T-9 | |
---|---|
Chemical name | 2-[4-(butylthio)-2,5-dimethoxyphenyl]ethanamine |
Chemical formula | C14H23NO2S |
CAS number | 207740-28-1 |
Molecular mass | ? |
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.
Contents |
[edit] 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.
[edit] Dosage
In his book PIHKAL (Phenethylamines I Have Known and Loved), Shulgin lists the dosage range as 60 - 100 mg.
[edit] 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.
[edit] 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.
[edit] 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.
[edit] 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.
[edit] External links
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
AEM, AL, Aleph, Aleph-2, Aleph-4, Aleph-6, Aleph-7, Ariadne, Asymbescaline, Buscaline, Beatrice, Bis-TOM, BOB, BOD, BOH, BOHD, BOM, 4-bromo-3,5-dimethoxyamphetamine, 2-bromo-4,5-methylenedioxyamphetamine, 2C-B, 3C-BZ, 2C-C, 2C-D, 2C-E, 3C-E, 2C-F, 2C-G, 2C-G-3, 2C-G-4, 2C-G-5, 2C-G-N, 2C-H, 2C-I, 2C-N, 2C-O-4, 2C-P, CPM, 2C-SE, 2C-T, 2C-T-2, 2C-T-4, psi-2C-T-4, 2C-T-7, 2C-T-8, 2C-T-9, 2C-T-13, 2C-T-15, 2C-T-17, 2C-T-21, 4-D, beta-D, DESOXY, 2,4-DMA, 2,5-DMA, 3,4-DMA, DMCPA, DME, DMMDA, DMMDA-2, DMPEA, DOAM, DOB, DOBU, DOC, DOEF, DOET, DOI, DOM, psi-DOM, DON, DOPR, Escaline, EEE, EEM, EME, EMM, Ethyl-J/EBDB, Ethyl-K, F-2, F-22, Flea, 3C-G-3, 3C-G-4, 3C-G-5, 3C-G-N, Ganesha, HOT-2, HOT-7, HOT-17, IDNNA, Isomescaline, Isoproscaline, Iris, J/BDB, Lophophine, Mescaline, 4-MA, Madam-6, Methallylescaline, MDA, MDAL, MDBU, MDBZ, MDCPM, MDDM, MDE, MDHOET, MDIP, MDMA, MDMC/EDMA, MDMEO, MDMEOET, MDMP, MDOH, MDPEA, MDPH, MDPL, MDPR, Metaescaline, MEDA, MEE, MEM, MEPEA, Meta-DOB, Meta-DOT, Methyl-DMA, Methyl-DOB, Methyl-J/MBDB, Methyl-K, Methyl-MA, Methyl-MMDA-2, MMDA, MMDA-2, MMDA-3a, MMDA-3b, MME, MP, MPM, Ortho-DOT Proscaline, Phenescaline, Phenethylamine, Propynyl, Symbescaline, 2,3,4,5-tetramethoxyamphetamine, 3-TASB, 4-TASB, 5-TASB, Thiobuscaline, 3-TE, 4-TE, 3-TIM, 4-TIM, 5-TIM, 3-TM, 4-TM, TMA, TMA-2, TMA-3, TMA-4, TMA-5, TMA-6, 3-TME, 4-TME, 5-TME, 2T-MMDA-3a, 4T-MMDA-2, TMPEA, 2-TOET, 5-TOET, 2-TOM, 5-TOM, TOMSO, Thioproscaline, Trisescaline, 3-TSB, 4-TSB, 3-T-Trisescaline, 4-T-Trisescaline