Levomethamphetamine
| Clinical data | |
|---|---|
| Trade names | Vicks VapoInhaler, Everclear Inhaler, others |
| Other names | l-methamphetamine; (-)-methamphetamine; (R)-methamphetamine; (R)-(-)-methamphetamine; l-desoxyephedrine; levodesoxyephedrine |
| Routes of administration | Medical: Intranasal Recreational: By mouth, intravenous, insufflation, inhalation, suppository |
| Drug class | Norepinephrine releasing agent; Decongestant |
| Legal status | |
| Legal status |
|
| Pharmacokinetic data | |
| Bioavailability | Oral: ~100% |
| Metabolism | Liver (CYP2D6) |
| Metabolites | Levoamphetamine |
| Elimination half-life | 10–15 hours |
| Excretion | Urine (41–49% unchanged, 2–3% as levoamphetamine) |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.046.974 |
| Chemical and physical data | |
| Formula | C10H15N |
| Molar mass | 149.237 g·mol−1 |
| 3D model (JSmol) | |
| Chirality | Levorotatory enantiomer |
| |
| |
| (verify) | |
Levomethamphetamine (INN: levmetamfetamine) is an optical isomer of methamphetamine primarily used as a topical nasal decongestant. Levomethamphetamine is used to treat nasal congestion from allergies and the common cold. It was first used medically as decongestant beginning in 1958 and has been used for such purposes, primarily in the United States, since then.