Anodyne

Aleph-7
2,5-Dimethoxy-4-propylthioamphetamine
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC14H23NO2S[1]
Molecular mass269.40 g/mol[1]
Predicted LogP3.1[1]
Chiralityracemic[2]
Identifiers
[]
IUPAC name1-(2,5-dimethoxy-4-propylsulfanylphenyl)propan-2-amine[1]
SMILESCCCSC1=C(C=C(C(=C1)OC)CC(C)N)OC[1]
InChIInChI=1S/C14H23NO2S/c1-5-6-18-14-9-12(16-3)11(7-10(2)15)8-13(14)17-4/h8-10H,5-7,15H2,1-4H3[1]
InChIKeyXHWDHFUBCVWXDZ-UHFFFAOYSA-N[1]
Dosing

2,5-Dimethoxy-4-propylthioamphetamine

2,5-Dimethoxy-4-propylthioamphetamine (also known as 4-propylthio-2,5-dimethoxyamphetamine, J2.489.044i, 2,5-Dimethoxy-α-methyl-4-(propylthio)benzeneethanamine, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-(propylthio)-, 2,5-dimethoxy-4-n-propylthioamphetamine or 2-(2,5-Dimethoxy-4-propylsulfanyl-phenyl)-1-methyl-ethylamine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Stereochemistry

(RS)-2,5-Dimethoxy-4-propylthioamphetamine is a racemic mixture of the optical stereoisomers

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 11197521, 2,5-Dimethoxy-4-propylthioamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/11197521.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-propylthioamphetamine. UNII: RB42O7HM6C. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/RB42O7HM6C