2,5-Dimethoxy-4-trifluoromethylamphetamine
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| Other names | 2,5-Dimethoxy-4-trifluoromethylamphetamine; 4-Trifluoromethyl-2,5-dimethoxyamphetamine; DOTFM; 3C-TFM |
| Routes of administration | Oral |
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| Duration of action | Unknown |
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| Formula | C12H16F3NO2 |
| Molar mass | 263.260 g·mol−1 |
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2,5-Dimethoxy-4-trifluoromethylamphetamine (DOTFM) is a psychedelic drug of the phenethylamine, amphetamine, and DOx (where 'x' indicates a 4-substitution on the phenyl group of 2,5-dimethoxyamphetamine) families. It was first synthesized in 1994 by a team at Purdue University led by David E. Nichols. DOTFM is the α-methylated analogue of 2C-TFM. It is the most potent DOx psychedelic.