Dimethylamphetamine

Dimethylamphetamine
INN: Dimetamfetamine

File:Dimethylamphetamine.svg
File:Dimetamfetamin.png
Clinical data
Routes of administration	Oral
ATC code	none
Legal status
Legal status	AU: S9 (Prohibited substance) US: Schedule I
Identifiers
IUPAC name N,N-dimethyl-1-phenylpropan-2-amine
CAS Number	4075-96-1 checkY
PubChem CID	20006
ChemSpider	18847 ☒N
UNII	IYE3F3MHCU
KEGG	C22825 checkY
E number	{{#property:P628}}
CompTox Dashboard (EPA)	{{#property:P3117}}
ECHA InfoCard	{{#property:P2566}}
Chemical and physical data
Formula	C11H17N
Molar mass	163.264 g·mol−1
3D model (JSmol)	Interactive image
SMILES CC(N(C)C)CC1=CC=CC=C1
InChI InChI=1S/C11H17N/c1-10(12(2)3)9-11-7-5-4-6-8-11/h4-8,10H,9H2,1-3H3 checkY Key:OBDSVYOSYSKVMX-UHFFFAOYSA-N checkY
☒NcheckY (what is this?)  (verify)

Dimethylamphetamine (Metrotonin), also known as dimetamfetamine (INN), dimephenopan and N,N-dimethylamphetamine, is a stimulant drug of the phenethylamine and amphetamine chemical classes. Dimethylamphetamine has weaker stimulant effects than amphetamine or methamphetamine and is considerably less addictive and less neurotoxic compared to methamphetamine. However, it still retains some mild stimulant effects and abuse potential, and is illegal in both the United States and Australia.

Dimethylamphetamine has occasionally been found in illicit methamphetamine laboratories, but is usually an impurity rather than the desired product. It may be produced by accident when methamphetamine is synthesised by N-methylation of dextroamphetamine if the reaction temperature is too high or an excess of methylating agent is used.

It is said to be a prodrug of methamphetamine and amphetamine, which are minor metabolites.

See also

• Substituted amphetamine

External links

• NNDMA (N,N-Dimethylamphetamine) - Isomer Design