DOTMA
Pharmaceutical compound
From Wikipedia, the free encyclopedia
DOTMA, also known as 2,5-dimethoxy-3,4,6-trimethylamphetamine or as Julia, is a psychedelic drug of the phenethylamine, amphetamine, and DOx families related to DOM.[1] It is the 3,6-dimethyl derivative of DOM and the 6-methyl derivative of Ganesha.[1] The drug is said to be the first and only known active phenethylamine psychedelic with a fully substituted phenyl ring.[1] However, the cyclized FLY phenethylamines such as 2C-B-FLY also have a fully substituted phenyl ring.[1]
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| Clinical data | |
|---|---|
| Other names | 2,5-Dimethoxy-3,4,6-trimethylamphetamine; Julia; 3,6-Dimethyl-DOM; 6-Methyl-Ganesha |
| Routes of administration | Oral[1] |
| Drug class | Serotonergic psychedelic; Hallucinogen |
| ATC code |
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| Pharmacokinetic data | |
| Duration of action | 7–9 hours[1] |
| Identifiers | |
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| Chemical and physical data | |
| Formula | C14H23NO2 |
| Molar mass | 237.343 g·mol−1 |
| 3D model (JSmol) | |
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DOTMA's dose is approximately 70 mg orally and its duration is 7 to 9 hours.[1] It is less potent than DOM, which is active at doses of 3 to 10 mg, and has a shorter duration than DOM, which lasts 14 to 20 hours.[1] Similarly, DOTMA is less potent and shorter-acting than Ganesha, which has a dose of 20 to 32 mg and a duration of 18 to 24 hours.[1]
DOTMA was described in the scientific literature by Daniel Trachsel in 2013.[1] The 6-methyl-DOM analogue of DOTMA and Ganesha, Juno, is relatively unknown but may be an active psychedelic as well.[1] DOTMA, or Julia, is closely related to Alexander Shulgin's "ten classic ladies".[2][3] It is a controlled substance in Canada due to phenethylamine blanket-ban language[4] but is not explicitly controlled in the United States.[5]
See also
- DOx (psychedelics)
- Juno (6-methyl-DOM)
- Ganesha (3-methyl-DOM)
- 2C-G (3-methyl-2C-D)
- PeMA
- TMePEA
- 2,6-Dimethylmescaline
- 2-Methylmescaline
- Xylopropamine (3,4-DMeA)
