| Speed | |
|---|---|
| Salts [] | |
|---|---|
| Amphetamine chlorphenoxyacetate | |
| Amphetamine hemisulfate | |
| Amphetamine hydrochloride | |
| Amphetamine adipate | |
| Amphetamine tartrate | |
| Amphetamine phosphate | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 135.21 g/mol [1] |
| Density | 0.913 at 77 °F (EPA, 1998) - Less dense than water; will float g/cm3 [1] |
| Appearance | Mobile liquid [1] |
| Odor | Amine odor [1] |
| Taste | Acrid, burning taste [1] |
| Melting point | 25 °C [1] |
| Boiling point | 392 to 397 °F at 760 mmHg (EPA, 1998) [1] |
| Decomposition | When heated to decomposition it emits toxic fumes of nitroxides. [1] |
| Solubility | Moderate solubility [1] |
| Predicted LogP | 1.8 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C9H13N [1] |
| IUPAC name | 1-phenylpropan-2-amine [1] |
| SMILES | CC(CC1=CC=CC=C1)N [1] |
| InChI | InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3 [1] |
| InChIKey | KWTSXDURSIMDCE-UHFFFAOYSA-N [1] |
Amphetamine
Amphetamine (also known as Amphetamine, Amfetamine, 1-Phenyl-2-aminopropane, 300-62-9, Desoxynorephedrine, Norephedrane, Elastonon, Fenopromin, Phenedrine or β-Aminopropylbenzene) is a stimulant substance of the amphetamine class.
Chemistry
Salts []
Amphetamine is typically found in the form of its chlorphenoxyacetate, hemisulfate, hydrochloride, adipate, tartrate and phosphate salts.
Stereochemistry []
Amphetamine is a racemic mixture of the enantiomers
Pharmacology
ATC Classification
In the nervous system (N) amphetamine acts as a stimulant (N06B), sympathomimetic (N06BA) and psychoanaleptic (N06).[1]Metabolism
Subjective effects []
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 3007, Amphetamine. Accessed February 11, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/3007
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Amphetamine. UNII: CK833KGX7E. Global Substance Registration System. Accessed February 11, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/CK833KGX7E