Dimethoxyamphetamine

From Self-sufficiency
Jump to: navigation, search
Dimethoxyamphetamine
File:2,4-DMA.png
File:DMA-3d-sticks.png
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.

Positional isomers

2,4-DMA

File:2,4-DMA.png
2,4-DMA, or 2,4-dimethoxy-amphetamine

Dosage: 60 mg or greater

Duration: short

Effects: stimulative, amphetamine-like effects

2,5-DMA

File:2,5-dma.png
2,5-DMA, or 2,5-dimethoxy-amphetamine

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

File:3,4-dma.png
3,4-DMA, or 3,4-dimethoxy-amphetamine

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

Cite error: Invalid <references> tag; parameter "group" is allowed only.

Use <references />, or <references group="..." />

External links

ru:3,4-диметоксиамфетамин
  1. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.