2,4-Dimethoxyamphetamine

2,4-Dimethoxyamphetamine

Clinical data
Other names	2,4-DMA; 2,4-Dimethoxy-α-methylphenethylamine; DMA-3
Identifiers
IUPAC name 1-(2,4-dimethoxyphenyl)propan-2-amine
CAS Number	23690-13-3 52850-81-4
PubChem CID	141047
ChemSpider	124411
UNII	GT33R7Q58G
ChEMBL	ChEMBL282734
CompTox Dashboard (EPA)	DTXSID90874252
Chemical and physical data
Formula	C11H17NO2
Molar mass	195.262 g·mol−1
3D model (JSmol)	Interactive image
SMILES CC(CC1=C(C=C(C=C1)OC)OC)N
InChI InChI=1S/C11H17NO2/c1-8(12)6-9-4-5-10(13-2)7-11(9)14-3/h4-5,7-8H,6,12H2,1-3H3 Key:DQWOZMUBHQPFFF-UHFFFAOYSA-N

2,4-Dimethoxyamphetamine (2,4-DMA), also known as DMA-3, is a drug of the phenethylamine and amphetamine families. ^{[1] [2]} It is one of the dimethoxyamphetamine (DMA) series of positional isomers. ^{[1] [2]}

It was reported by Alexander Shulgin to be active at a dose of 60 mg orally and to produce threshold amphetamine-like stimulant and euphoric effects. ^{[1] [2]} However, there was also a "diffusion of association" and Shulgin stated that it was more than just a stimulant. ^[1] The duration was described as short and effects subsiding at 3 hours. ^{[1] [2]} Per Shulgin, the drug could be a full stimulant and/or a full psychedelic at sufficiently high doses, but higher doses were not pursued. ^[1]

See also

• 2,4,5-Trimethoxyamphetamine

References

1. Shulgin AT, Shulgin A (1991). "#53 2,4-DMA; 2,4-DIMETHOXYAMPHETAMINE". PiHKAL: A Chemical Love Story (1st ed.). Berkeley, CA: Transform Press. ISBN   9780963009609. OCLC   25627628.
2. Shulgin A, Manning T, Daley PF (2011). "#35. 2,4-DMA". The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds . Vol. 1. Berkeley: Transform Press. ISBN   978-0-9630096-3-0.