Anodyne

Epinine

Salts []
Hydrobromide

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via JSmol

Physical properties []
Molecular mass	167.20 g/mol ^[1]
Melting point	188 - 189 °C ^[1]
Predicted LogP	-0.5 ^[1]

Structural Identifiers []
Molecular formula	C₉H₁₃NO₂ ^[1]
IUPAC name	4-[2-(methylamino)ethyl]benzene-1,2-diol ^[1]
SMILES	CNCCC1=CC(=C(C=C1)O)O ^[1]
InChI	InChI=1S/C9H13NO2/c1-10-5-4-7-2-3-8(11)9(12)6-7/h2-3,6,10-12H,4-5H2,1H3 ^[1]
InChIKey	NGKZFDYBISXGGS-UHFFFAOYSA-N ^[1]

Epinine

(Redirected from Deoxyepinephrine)

Epinine (also known as deoxyepinephrine, Desoxyepinephrine, Deoxyadrenaline, Epyamine, Epinin, Deoxyephinephrine, 1,2-Benzenediol, 4-(2-(methylamino)ethyl)-, 4-(2-Methylamino-ethyl)-benzene-1,2-diol, 3,4-dihydroxy-N-methylphenethylamine or N-methyl-3,4-dihydroxyphenethylamine) is a sympathomimetic and neurotransmitter substance of the phenethylamine class.

Chemistry

Salts []

Epinine is typically found in the form of its hydrobromide salt.

Stereochemistry []

Epinine is a achiral mixture

Subjective effects []

Physical effects
Abnormal heartbeat Dehydration Dry mouth Increased blood pressure Increased heart rate Restless legs Shakiness Stamina enhancement Vasoconstriction

Cognitive effects
Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 4382, Epinine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4382
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Epinine. UNII: R7339QLN1C. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/R7339QLN1C