Dimethoxyamphetamine
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Dimethoxyamphetamine"
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Dimethoxyamphetamine
IUPAC name 2-(2,4-Dimethoxy-phenyl)-1-methyl-ethylamine
Identifiers
CAS number
SMILES
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 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

2,4-DMA, or 2,4-dimethoxy-amphetamine
2,4-DMA, or 2,4-dimethoxy-amphetamine


Dosage: 60 mg or greater

Duration: short

Effects: stimulative, amphetamine-like effects

2,5-DMA

2,5-DMA, or 2,5-dimethoxy-amphetamine
2,5-DMA, or 2,5-dimethoxy-amphetamine


The DO analogue of 2C-H (DOH)

Dosage: 80-160 mg

Duration: 6-8 hours

Effects: Mydriasis, increase in heart rate

3,4-DMA

3,4-DMA, or 3,4-dimethoxy-amphetamine
3,4-DMA, or 3,4-dimethoxy-amphetamine


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.

References

See also

External links


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