DOM | |
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Salts [] | |
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2,5-Dimethoxy-4-methylamphetamine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C12H19NO2[1] |
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Molecular mass | 209.28 g/mol[1] |
Predicted LogP | 2.2[1] |
Melting point | 60.5 to 60.1 °C[1] |
Decomposition | When heated to decomposition it emits toxic vapors of /Nitrogen oxides/.[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(2,5-dimethoxy-4-methylphenyl)propan-2-amine[1] |
SMILES | CC1=CC(=C(C=C1OC)CC(C)N)OC[1] |
InChI | InChI=1S/C12H19NO2/c1-8-5-12(15-4)10(6-9(2)13)7-11(8)14-3/h5,7,9H,6,13H2,1-4H3[1] |
InChIKey | NTJQREUGJKIARY-UHFFFAOYSA-N[1] |
Dosing |
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2,5-Dimethoxy-4-methylamphetamine
2,5-Dimethoxy-4-methylamphetamine (also known as STP, (RS)-DOM, 4-Methyl-2,5-dimethoxyamphetamine, 2,5-Dimethoxymethylamphetamine, 2',5'-Dimethoxy-4'-methylamphetamine, 2,5-Dimethoxy-4-methylphenylisopropylamine, -DOM, 2,5-Dimethoxy-4,α-dimethylphenethylamin, -2,5-Dimethoxy-4-methylamphetamine or -1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.
Chemistry
2,5-Dimethoxy-4-methylamphetamine is typically found in the form of its hydrochloride salt.
Stereochemistry
(RS)-2,5-Dimethoxy-4-methylamphetamine is a racemic mixture of the optical stereoisomers:
Stereoisomers [] |
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Legal status
- Australia: 2,5-Dimethoxy-4-methylamphetamine is a S9.
- Brazil: 2,5-Dimethoxy-4-methylamphetamine is a F2.[3]
- Canada: 2,5-Dimethoxy-4-methylamphetamine is a Schedule I.
- United Kingdom: 2,5-Dimethoxy-4-methylamphetamine is a Class A.
- United States: 2,5-Dimethoxy-4-methylamphetamine is a Schedule I under the "Controlled Substances Act (CSA)".
See also
External links
- 2,5-Dimethoxy-4-methylamphetamine (Wikipedia)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (Wikidata)
- 2,5-Dimethoxy-4-methylamphetamine (DrugBank)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (PubChem)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (ChEMBL)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-methylamphetamine (HMDB)
- 2,5-Dimethoxy-4-methylamphetamine (KEGG)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (UNII)
- 2,5-Dimethoxy-4-methylamphetamine / (+)-2,5-Dimethoxy-4-methylamphetamine / (-)-2,5-Dimethoxy-4-methylamphetamine (EPA DSSTox)
References
National Center for Biotechnology Information. PubChem Compound Summary for CID 85875, 2,5-Dimethoxy-4-methylamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/85875.
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-methylamphetamine. UNII: UKI9MLD5OI. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/UKI9MLD5OI
Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. July 24, 2023. Accessed June 17, 2025. https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451