DOET | |
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Salts [] | |
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2,5-Dimethoxy-4-ethylamphetamine sulfate | |
2,5-Dimethoxy-4-ethylamphetamine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C13H21NO2[1] |
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Molecular mass | 223.31 g/mol[1] |
Predicted LogP | 2.8[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(4-ethyl-2,5-dimethoxyphenyl)propan-2-amine[1] |
SMILES | CCC1=CC(=C(C=C1OC)CC(C)N)OC[1] |
InChI | InChI=1S/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3[1] |
InChIKey | HXJKWPGVENNMCC-UHFFFAOYSA-N[1] |
Dosing | |
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Duration of action | 5–20 hours |
2,5-Dimethoxy-4-ethylamphetamine
2,5-Dimethoxy-4-ethylamphetamine (also known as 4-Ethyl-2,5-dimethoxyamphetamine, HECATE, J71.136E, -1-(2,5-Dimethoxy-4-ethylphenyl)-2-aminopropane, -4-Ethyl-2,5-dimethoxy-α-methylphenethylamine, hxjkwpgvennmcc-uhfffaoysa-n, Benzeneethanamine, 4-ethyl-2,5-dimethoxy-α-methyl-, 2,5-Dimethoxy-4-ethylamphetamin, Ncgc00247691-01 or DOET,(-)) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.
Chemistry
2,5-Dimethoxy-4-ethylamphetamine is typically found in the form of its sulfate and hydrochloride salts.
Stereochemistry
(RS)-2,5-Dimethoxy-4-ethylamphetamine is a racemic mixture of the optical stereoisomers:
Stereoisomers [] |
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Legal status
- Australia: 2,5-Dimethoxy-4-ethylamphetamine is a Schedule 9.
- Brazil: 2,5-Dimethoxy-4-ethylamphetamine is a F2.[3]
- Canada: 2,5-Dimethoxy-4-ethylamphetamine is a Schedule I.
- Germany: 2,5-Dimethoxy-4-ethylamphetamine is a Anlage I.
- United Nations: 2,5-Dimethoxy-4-ethylamphetamine is a Schedule I under the "Convention on Psychotropic Substances 1971".
- United States: 2,5-Dimethoxy-4-ethylamphetamine is a Schedule I under the "Controlled Substances Act (CSA)".
- United Kingdom: 2,5-Dimethoxy-4-ethylamphetamine is a Class A.
See also
External links
- 2,5-Dimethoxy-4-ethylamphetamine (Wikipedia)
- 2,5-Dimethoxy-4-ethylamphetamine (Wikidata)
- 2,5-Dimethoxy-4-ethylamphetamine (DrugBank)
- 2,5-Dimethoxy-4-ethylamphetamine / (+)-2,5-Dimethoxy-4-ethylamphetamine / (-)-2,5-Dimethoxy-4-ethylamphetamine (PubChem)
- 2,5-Dimethoxy-4-ethylamphetamine / (+)-2,5-Dimethoxy-4-ethylamphetamine / (-)-2,5-Dimethoxy-4-ethylamphetamine (ChEMBL)
- 2,5-Dimethoxy-4-ethylamphetamine (ChEBI)
- 2,5-Dimethoxy-4-ethylamphetamine / (+)-2,5-Dimethoxy-4-ethylamphetamine / (-)-2,5-Dimethoxy-4-ethylamphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-ethylamphetamine (KEGG)
- 2,5-Dimethoxy-4-ethylamphetamine / (+)-2,5-Dimethoxy-4-ethylamphetamine / (-)-2,5-Dimethoxy-4-ethylamphetamine (UNII)
- 2,5-Dimethoxy-4-ethylamphetamine (EPA DSSTox)
References
National Center for Biotechnology Information. PubChem Compound Summary for CID 27402, 2,5-Dimethoxy-4-ethylamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/27402.
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-ethylamphetamine. UNII: 9SK6K682UL. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9SK6K682UL
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