NM-αMT

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	188.27 g/mol ^[1]
Predicted LogP	2.5 ^[1]

Structural Identifiers []
Molecular formula	C₁₂H₁₆N₂ ^[1]
IUPAC name	1-(1H-indol-3-yl)-N-methylpropan-2-amine ^[1]
SMILES	CC(CC1=CNC2=CC=CC=C21)NC ^[1]
InChI	InChI=1S/C12H16N2/c1-9(13-2)7-10-8-14-12-6-4-3-5-11(10)12/h3-6,8-9,13-14H,7H2,1-2H3 ^[1]
InChIKey	HUWIYJREHSBOEO-UHFFFAOYSA-N ^[1]

α,N-Dimethyltryptamine

α,N-Dimethyltryptamine (also known as n,α-dimethyltryptamine, α,N-DMT, α,N-dimethyltryptamine, N,α-Dimethyltryptamine, Niosh/nl8480000, SKF-7024, RO-3-1715, NL84800000, -N,α-Dimethyl-1H-indole-3-ethanamine or 1H-Indole-3-ethanamine, N,α-dimethyl-, (+-)-) is a stimulant substance of the α-alkyltryptamine class.

Chemistry

Stereochemistry []

(RS)-α,N-Dimethyltryptamine 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 3724428, α,N-Dimethyltryptamine. Accessed July 3, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/3724428
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. α,N-Dimethyltryptamine. UNII: L8WKV7YXX3. Global Substance Registration System. Accessed July 3, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/L8WKV7YXX3

Anodyne