AnodyneWiki

Heptaminol

Heptaminol

Salts []
Heptaminol hydrochloride

Molecular structure via molpic based on CDK

Rotamer []

Conformer structure via 3Dmol.js

Physical properties []
Molecular mass	145.24 g/mol ^[1]
Predicted LogP	0.7 ^[1]

Structural Identifiers []
Molecular formula	C₈H₁₉NO ^[1]
IUPAC name	6-amino-2-methylheptan-2-ol ^[1]
SMILES	CC(CCCC(C)(C)O)N ^[1]
InChI	InChI=1S/C8H19NO/c1-7(9)5-4-6-8(2,3)10/h7,10H,4-6,9H2,1-3H3 ^[1]
InChIKey	LREQLEBVOXIEOM-UHFFFAOYSA-N ^[1]

Heptaminol (also known as 6-Amino-2-methyl-2-heptanol, Corasore, Heptaminolum, Ginkor, 2-Heptanol, 6-amino-2-methyl-, eptaminolo, Gincor-fort, acAfylline heptaminol, Dtxcid0028458 or C01DX08) is a sympathomimetic substance of the amine class.

Chemistry

Salts []

Heptaminol is typically found in the form of its hydrochloride salt.

Stereochemistry []

Heptaminol is a racemic mixture of the enantiomers.

Stereoisomerism
(R)-Heptaminol (S)-Heptaminol
Stereoisomer enumberation with rdkit

Pharmacology

ATC Classification

In the cardiovascular system (C) heptaminol acts

Subjective effects []

class / Sympathomimetic

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 3590, Heptaminol. Accessed August 22, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/3590
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Heptaminol. UNII: 3DQS188SY5. Global Substance Registration System. Accessed August 22, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/3DQS188SY5