Hexedrone

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	205.30 g/mol ^[1]
Predicted LogP	3 ^[1]

Structural Identifiers []
Molecular formula	C₁₃H₁₉NO ^[1]
IUPAC name	2-(methylamino)-1-phenylhexan-1-one ^[1]
SMILES	CCCCC(C(=O)C1=CC=CC=C1)NC ^[1]
InChI	InChI=1S/C13H19NO/c1-3-4-10-12(14-2)13(15)11-8-6-5-7-9-11/h5-9,12,14H,3-4,10H2,1-2H3 ^[1]
InChIKey	BHIZKPHLTVLXIV-UHFFFAOYSA-N ^[1]

Hexedrone

Hexedrone (also known as 2-(Methylamino)-1-phenyl-1-hexanone, 1-Hexanone, 2-(methylamino)-1-phenyl-, α-Methylamino-caprophenone or 2-methylamino-1-(phenyl)hexan-1-one) is a stimulant substance of the cathinone class.

Chemistry

Stereochemistry []

(RS)-Hexedrone is a racemic mixture of the optical stereoisomers

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 129844496, Hexedrone. Accessed June 26, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/129844496
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Hexedrone. UNII: KLF7T8YQP5. Global Substance Registration System. Accessed June 26, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/KLF7T8YQP5

Anodyne