Anodyne

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DMPEA
3,4-Dimethoxyphenethylamine
Molecular structure via molpic
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Physical properties
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Molecular mass181.23 g/mol [1]
Predicted LogP0.8 [1]
Boiling point163 - 165 °C [1]
Solubility24.8 [ug/mL] (The mean of the results at pH 7.4) [1]
Structural Identifiers
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Molecular formulaC10H15NO2 [1]
IUPAC name2-(3,4-dimethoxyphenyl)ethanamine [1]
SMILESCOC1=C(C=C(C=C1)CCN)OC [1]
InChIInChI=1S/C10H15NO2/c1-12-9-4-3-8(5-6-11)7-10(9)13-2/h3-4,7H,5-6,11H2,1-2H3 [1]
InChIKeyANOUKFYBOAKOIR-UHFFFAOYSA-N [1]
Dosing

3,4-Dimethoxyphenethylamine

3,4-Dimethoxyphenethylamine (also known as Homoveratrylamine, Benzeneethanamine, 3,4-dimethoxy-, 3,4-Dimethoxyphenylethylamine, 2-(3,4-Dimethoxyphenyl)ethylamine, Dimethoxydopamine, Dimethylmescaline, Dopamine dimethyl ether, DIMPEA, O,O-Dimethyldopamine or 3,4-Dimethoxybenzeneethanamine) is a monoamine oxidase inhibitor substance of the catecholamine class.

Chemistry

Salts []

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

See also []

  • Substituted catecholamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 8421, 3,4-Dimethoxyphenethylamine. Accessed June 26, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/8421

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3,4-Dimethoxyphenethylamine. UNII: IQF9T435OP. Global Substance Registration System. Accessed June 26, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/IQF9T435OP