DMPEA

Salts []
3,4-Dimethoxyphenethylamine hydrochloride
3,4-Dimethoxyphenethylamine hydrobromide

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C10H15NO2[1]
Molecular mass	181.23 g/mol[1]
Predicted LogP	0.8[1]
Boiling point	163 - 165 °C[1]
Solubility	24.8 [ug/mL] (The mean of the results at pH 7.4)[1]
Chirality	achiral[2]

Identifiers []
IUPAC name	2-(3,4-dimethoxyphenyl)ethanamine[1]
SMILES	COC1=C(C=C(C=C1)CCN)OC[1]
InChI	InChI=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]
InChIKey	ANOUKFYBOAKOIR-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

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

Stereochemistry

3,4-Dimethoxyphenethylamine is a achiral mixture

See also

• Substituted catecholamines
• Anodyne

External links

• 3,4-Dimethoxyphenethylamine (Wikipedia)
• 3,4-Dimethoxyphenethylamine (Wikidata)
• 3,4-Dimethoxyphenethylamine (PubChem)
• 3,4-Dimethoxyphenethylamine (ChEMBL)
• 3,4-Dimethoxyphenethylamine (ChEBI)
• 3,4-Dimethoxyphenethylamine (Common Chemistry)
• 3,4-Dimethoxyphenethylamine (HMDB)
• 3,4-Dimethoxyphenethylamine (UNII)
• 3,4-Dimethoxyphenethylamine (EPA DSSTox)

References