2,5-Dimethoxy-4-trifluoromethylamphetamine

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2,5-Dimethoxy-4-trifluoromethylamphetamine
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Systematic (IUPAC) name
(RS)-1-[2,5-dimethoxy-4-(trifluoromethyl)phenyl]propan-2-amine
Legal status
Legal status
  • Uncontrolled
Identifiers
PubChem CID 10400521
ChemSpider 8575959
Synonyms 2,5-dimethoxy-4-trifluoromethylamphetamine
Chemical data
Formula C12H16F3NO2
Molar mass 263.26 g/mol
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2,5-Dimethoxy-4-trifluoromethylamphetamine (DOTFM) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized in 1994 by a team at Purdue University led by David E. Nichols.[1] DOTFM is the alpha-methylated analogue of 2C-TFM, and is around twice as potent in animal studies. It acts as an agonist at the 5HT2A and 5HT2C receptors. In drug-substitution experiments in rats, DOTFM fully substituted for LSD and was slightly more potent than DOI.[1] Anecdotal reports from human users suggest that DOTFM is a potent psychedelic with an extremely long duration of action, similar to Br-DFLY.

See also

References

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