Dimethoxyamphetamine
| Dimethoxyamphetamine | |
|---|---|
| File:2,4-DMA.png | |
| File:DMA-3d-sticks.png | |
| 2-(3,4-Dimethoxyphenyl)propylamine | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="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, 100 kPa) | |
| 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
2,4-DMA
Dosage: 60 mg or greater
Duration: short
Effects: stimulative, amphetamine-like effects
2,5-DMA
The DO analogue of 2C-H (DOH)
CAS Number: 2801-68-5
Dosage: 80–160 mg
Duration: 6–8 hours
Effects: Mydriasis, increase in heart rate
3,4-DMA
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
References
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<references />, or <references group="..." />External links
- 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
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