Anodyne

MDPEA
3,4-Methylenedioxyphenethylamine
Salts
[]
3,4-Methylenedioxyphenethylamine hemisulfate
3,4-Methylenedioxyphenethylamine hemisulfate
3,4-Methylenedioxyphenethylamine hydrochloride
3,4-Methylenedioxyphenethylamine hydrochloride
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC9H11NO2[1]
Molecular mass165.19 g/mol[1]
Predicted LogP1.2[1]
Chiralityachiral[2]
Identifiers
[]
IUPAC name2-(1,3-benzodioxol-5-yl)ethanamine[1]
SMILESC1OC2=C(O1)C=C(C=C2)CCN[1]
InChIInChI=1S/C9H11NO2/c10-4-3-7-1-2-8-9(5-7)12-6-11-8/h1-2,5H,3-4,6,10H2[1]
InChIKeyRRIRDPSOCUCGBV-UHFFFAOYSA-N[1]
Dosing

3,4-Methylenedioxyphenethylamine

3,4-Methylenedioxyphenethylamine (also known as Homopiperonylamine, 1,3-benzodioxole-5-ethanamine, Methylenedioxyphenethylamine, Methylenedioxyphenylethylamine, Phenethylamine, 3,4-methylenedioxy-, Phenethylamine, 3,4-(methylenedioxy)-, 2-(3,4-Methylenedioxyphenyl)ethylamine, 3,4-MDPEA, 5-19-08-00407 or 3,4-(Methylenedioxy)phenethylamine) is a substance of the methylenedioxyphenethylamine class.

Chemistry

3,4-Methylenedioxyphenethylamine is typically found in the form of its hemisulfate and hydrochloride salts.

Stereochemistry

3,4-Methylenedioxyphenethylamine is a achiral mixture

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 73874, 3,4-Methylenedioxyphenethylamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/73874.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3,4-Methylenedioxyphenethylamine. UNII: F2J2U8J2G5. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/F2J2U8J2G5