Dimethoxyamphetamine
From Wikipedia, the free encyclopedia
| Dimethoxyamphetamine | |
|---|---|
 |
|
 |
|
| IUPAC name | 2-(2,4-Dimethoxy-phenyl)-1-methyl-ethylamine |
| Identifiers | |
| CAS number | |
| SMILES | C1(=CC(=CC=C1CC(C)N)OC)OC |
| Properties | |
| Molecular formula | C11H17NO2 |
| Molar mass | 195.261 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
DMA, or dimethoxyamphetamine, is a series of lesser-known psychedelic drugs similar in structure to amphetamine and to trimethoxyamphetamine (TMA). They were first synthesized by Alexander Shulgin and written up in his book PiHKAL (Phenethylamines i Have Known And Loved).[1] Very little data is known about their dangers or toxicity.
Contents |
[edit] Positional isomers
[edit] 2,4-DMA
Dosage: 60 mg or greater
Duration: short
Effects: stimulative, amphetamine-like effects
[edit] 2,5-DMA
The DO analogue of 2C-H (DOH)
Dosage: 80-160 mg
Duration: 6-8 hours
Effects: Mydriasis, increase in heart rate
[edit] 3,4-DMA
Dosage: unknown
Duration: unknown
Effects: Mescaline-like hallucinations
Note that two other positional isomers of dimethoxyamphetamine, 2,6-DMA and 3,5-DMA, have also been made, but these drugs have not been tested in humans and their effects are unknown. However, it is likely that these compounds would also produce amphetamine-like stimulation or possibly hallucinogenic effects.
[edit] References
- ^ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
