Dimethoxyamphetamine
| Dimethoxyamphetamine | |
|---|---|
 |
|
 |
|
|
2-(3,4-Dimethoxyphenyl)propylamine |
|
| Identifiers | |
| PubChem | 91255 |
| ChemSpider | 82404  |
| ChEMBL | CHEMBL280855 |
| Jmol-3D images | Image 1 Image 2 |
|
|
|
|
| Properties | |
| Molecular formula | C11H17NO2 |
| Molar mass | 195.26 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
 (verify) (what is:  / ?) |
|
| Infobox 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
Positional isomers[edit]
2,4-DMA[edit]
Dosage: 60 mg or greater
Duration: short
Effects: stimulative, amphetamine-like effects
2,5-DMA[edit]
The DO analogue of 2C-H (DOH)
CAS Number: 2801-68-5
Dosage: 80–160 mg[2]
Duration: 6–8 hours
Effects: Mydriasis, increase in heart rate
3,4-DMA[edit]
Dosage: unknown
Duration: unknown
Effects: Mescaline-like visuals
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.
See also[edit]
References[edit]
- ^ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
- ^ "PiHKAL". isomerdesign.com. Retrieved 2012-03-17.
External links[edit]
- 2,4-DMA Entry in PiHKAL
- 2,4-DMA Entry in PiHKAL • info
- 2,5-DMA Entry in PiHKAL
- 2,5-DMA Entry in PiHKAL • info
- 3,4-DMA Entry in PiHKAL
- 3,4-DMA Entry in PiHKAL • info
