DOPR | |
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Salts [] | |
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2,5-Dimethoxy-4-propylamphetamine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C14H23NO2[1] |
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Molecular mass | 237.34 g/mol[1] |
Predicted LogP | 3.4[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(2,5-dimethoxy-4-propylphenyl)propan-2-amine[1] |
SMILES | CCCC1=CC(=C(C=C1OC)CC(C)N)OC[1] |
InChI | InChI=1S/C14H23NO2/c1-5-6-11-8-14(17-4)12(7-10(2)15)9-13(11)16-3/h8-10H,5-7,15H2,1-4H3[1] |
InChIKey | UEEAUFJYLUJWQJ-UHFFFAOYSA-N[1] |
Dosing | |
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Duration of action | 20–30 hours |
2,5-Dimethoxy-4-propylamphetamine
2,5-Dimethoxy-4-propylamphetamine (also known as J273.474E, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-propyl-, -1-(2,5-Dimethoxy-4-n-propylphenyl)-2-aminopropane, ueeaufjylujwqj-uhfffaoysa-n, -1-(2,5-Dimethoxy-4-N-propylphenyl)-2-aminopropane, Dopr, Pdsp1_000459, Pdsp2_000457, 1-(2,5-Dimethoxy-4-propylphenyl)-2-propanamine # or 2,5-Dimethoxy-α-methyl-4-propylbenzeneethaneamine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.
Chemistry
2,5-Dimethoxy-4-propylamphetamine is typically found in the form of its hydrochloride salt.
Stereochemistry
(RS)-2,5-Dimethoxy-4-propylamphetamine is a racemic mixture of the optical stereoisomers
Legal status
- Canada: 2,5-Dimethoxy-4-propylamphetamine is a Schedule I.
- Germany: 2,5-Dimethoxy-4-propylamphetamine is a Neuer-Psychoaktiver-Stoff under the "Neue-psychoaktive-Stoffe-Gesetz (NpSG)".
- United Kingdom: 2,5-Dimethoxy-4-propylamphetamine is a Class A.
See also
External links
- 2,5-Dimethoxy-4-propylamphetamine (Wikipedia)
- 2,5-Dimethoxy-4-propylamphetamine (Wikidata)
- 2,5-Dimethoxy-4-propylamphetamine (PubChem)
- 2,5-Dimethoxy-4-propylamphetamine (ChEMBL)
- 2,5-Dimethoxy-4-propylamphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-propylamphetamine (UNII)
- 2,5-Dimethoxy-4-propylamphetamine (EPA DSSTox)
References
National Center for Biotechnology Information. PubChem Compound Summary for CID 542051, 2,5-Dimethoxy-4-propylamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/542051.
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-propylamphetamine. UNII: L3P287BI9W. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/L3P287BI9W