| Weight | 163.264 g/mol |
|---|---|
| Formula | C11H17N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Dimethylamphetamine (49681-82-5, 4075-96-1)
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- A review of impurity profiling and synthetic route of manufacture of methylamphetamine, 3,4-methylenedioxymethylamphetamine, amphetamine, dimethylamphetamine and p-methoxyamphetamine (Forensic Science International, 2013)
- Discrimination of dimethylamphetamine and methamphetamine use: simultaneous determination of dimethylamphetamine-N-oxide and other metabolites in urine by high-performance liquid chromatography-electrospray ionization mass spectrometry. (Journal of Analytical Toxicology, 2000)
- Comparison of Reactivity of Amphetamine, Methamphetamine, and Dimethylamphetamine with Lactose and Related Compounds (Journal of Pharmaceutical Sciences, 1965)
- The metabolism of dimethylamphetamine in rat and man (Xenobiotica, 1987)
- Analysis of Pyrolysis Products of Dimethylamphetamine (Journal of Analytical Toxicology, 2001)
- Analysis of dimethylamphetamine and its metabolites in human urine by liquid chromatography-electrospray ionization-mass spectrometry with direct sample injection. (Forensic Science International, 2002)
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SMILESCC(CC1=CC=CC=C1)N(C)C
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InChIKeyOBDSVYOSYSKVMX-UHFFFAOYSA-N
- Pubchem - Dimethylamphetamine
- Wikipedia - Dimethylamphetamine
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 a Schedule I controlled drug.
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