Anodyne

βk-5Cl-NM-αMT

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via JSmol

Physical properties []
Molecular mass	236.70 g/mol ^[1]
Predicted LogP	2.4 ^[1]

Structural Identifiers []
Molecular formula	C₁₂H₁₃ClN₂O ^[1]
IUPAC name	1-(5-chloro-1H-indol-3-yl)-2-(methylamino)propan-1-one ^[1]
SMILES	CC(C(=O)C1=CNC2=C1C=C(C=C2)Cl)NC ^[1]
InChI	InChI=1S/C12H13ClN2O/c1-7(14-2)12(16)10-6-15-11-4-3-8(13)5-9(10)11/h3-7,14-15H,1-2H3 ^[1]
InChIKey	JNYZOLQTXCZJRL-UHFFFAOYSA-N ^[1]

α,N-Dimethyl-5-chloro-β-ketotryptamine

α,N-Dimethyl-5-chloro-β-ketotryptamine is a entactogen substance of the tryptamine class.

Chemistry

Stereochemistry []

α,N-Dimethyl-5-chloro-β-ketotryptamine is a racemic mixture of the enantiomers

Stereoisomers
(R)-α,N-Dimethyl-5-chloro-β-ketotryptamine (S)-α,N-Dimethyl-5-chloro-β-ketotryptamine

Subjective effects []

Physical effects
Increased libido Restless legs Shakiness Teeth grinding

Cognitive effects
Cognitive euphoria Disinhibition Empathy, effection, and sociability enhancement Increased music appreciation

See also []

Substituted tryptamines

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 162765502, α,N-Dimethyl-5-chloro-β-ketotryptamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/162765502