Anodyne

TMA, TMA-1, 3,4,5-TMA
Generated by the Chemistry Development Kit (http://github.com/cdk)
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%!s() hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via 3Dmol.js
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Physical properties
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225.28 g/mol [1]
1.2 [1]
Structural Identifiers
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C12H19NO3 [1]
1-(3,4,5-trimethoxyphenyl)propan-2-amine [1]
CC(CC1=CC(=C(C(=C1)OC)OC)OC)N [1]
InChI=1S/C12H19NO3/c1-8(13)5-9-6-10(14-2)12(16-4)11(7-9)15-3/h6-8H,5,13H2,1-4H3 [1]
InChIKeyWGTASENVNYJZBK-UHFFFAOYSA-N [1]
Toxicity
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Human:
- oral: 800 μg/kg
Mouse:
- intraperitoneal: 200 mg/kg

3,4,5-Trimethoxyamphetamine

3,4,5-Trimethoxyamphetamine (also known as 3,4,5-Trimethoxyamphetamine, Trimethoxyamphetamine, α-Methylmescaline, Trimethoxyphenyl-β-aminopropane, 3,4,5-Trimethoxyphenyl-β-aminopropane, Phenethylamine, 3,4,5-trimethoxy-α-methyl-, Phenethylamine, α-methyl-3,4,5-trimethoxy-, Benzeneethanamine, 3,4,5-trimethoxy-α-methyl-, 1-(3,4,5-Trimethoxyphenyl)-2-aminopropane or J13.144J) is a psychedelic substance of the 3,5-dimethoxyamphetamine class.

Chemistry

Salts []

3,4,5-Trimethoxyamphetamine is typically found in the form of its hydrochloride salt.

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3,4,5-Trimethoxyamphetamine is a racemic mixture of the

Stereoisomers
(R)-3,4,5-TrimethoxyamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-3,4,5-TrimethoxyamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 31016, 3,4,5-Trimethoxyamphetamine. Accessed August 12, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/31016

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3,4,5-Trimethoxyamphetamine. UNII: P2K02L3YON. Global Substance Registration System. Accessed August 12, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/P2K02L3YON