Anodyne

DOPR
2,5-Dimethoxy-4-propylamphetamine
Salts
[]
2,5-Dimethoxy-4-propylamphetamine hydrochloride
2,5-Dimethoxy-4-propylamphetamine hydrochloride
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC14H23NO2[1]
Molecular mass237.34 g/mol[1]
Predicted LogP3.4[1]
Chiralityracemic[2]
Identifiers
[]
IUPAC name1-(2,5-dimethoxy-4-propylphenyl)propan-2-amine[1]
SMILESCCCC1=CC(=C(C=C1OC)CC(C)N)OC[1]
InChIInChI=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]
InChIKeyUEEAUFJYLUJWQJ-UHFFFAOYSA-N[1]
Dosing
Duration of action20–30 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

See also

References

  1. 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.

  2. 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