| TMA, TMA-1, 3,4,5-TMA | |
|---|---|
| Salts [] | |
|---|---|
| %!s( | |
| Molecular structure via molpic based on CDK |
| Rotamer [] | |
|---|---|
| Conformer structure via 3Dmol.js |
| Physical properties [] | |
|---|---|
| Molecular mass | 225.28 g/mol [1] |
| Predicted LogP | 1.2 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C12H19NO3 [1] |
| IUPAC name | 1-(3,4,5-trimethoxyphenyl)propan-2-amine [1] |
| SMILES | CC(CC1=CC(=C(C(=C1)OC)OC)OC)N [1] |
| InChI | 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] |
| InChIKey | WGTASENVNYJZBK-UHFFFAOYSA-N [1] |
| Toxicity [] | |
|---|---|
| TDLo | Human: - oral: 800 μg/kg |
| LDLo | 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.
Stereochemistry []
3,4,5-Trimethoxyamphetamine is a racemic mixture of the enantiomers
See also []
External links []
- 3,4,5-Trimethoxyamphetamine (Wikipedia)
- 3,4,5-Trimethoxyamphetamine (DrugBank)
- 3,4,5-Trimethoxyamphetamine (PubChem)
- 3,4,5-Trimethoxyamphetamine (ChEMBL)
- 3,4,5-Trimethoxyamphetamine (Probes & Drugs)
- 3,4,5-Trimethoxyamphetamine (Common Chemistry)
- 3,4,5-Trimethoxyamphetamine (KEGG)
- 3,4,5-Trimethoxyamphetamine (UNII)
- 3,4,5-Trimethoxyamphetamine (EPA DSSTox)
References []
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
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
Anodyne