DOTMA

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] Its dose is approximately 70 mg orally and its duration is 7 to 9 hours.^[1] DOTMA 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 is relatively unknown but may be an active psychedelic as well.^[1]

DOTMA

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	None
Pharmacokinetic data
Duration of action	7–9 hours[1]
Identifiers
IUPAC name 1-(2,5-dimethoxy-3,4,6-trimethylphenyl)propan-2-amine
Chemical and physical data
Formula	C14H23NO2
Molar mass	237.343 g·mol−1
3D model (JSmol)	Interactive image
SMILES COc1c(C)c(CC(N)C)c(c(c1C)C)OC
InChI InChI=1S/C14H23NO2/c1-8(15)7-12-11(4)13(16-5)9(2)10(3)14(12)17-6/h8H,7,15H2,1-6H3 Key:ROGMRKPRWZWOSW-UHFFFAOYSA-N

See also

• DOx
• Ganesha
• 2C-G
• PeMA
• TMePEA
• Xylopropamine