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| ORPHENADRINE HYDROCHLORIDE Basic information |
Product Name: | ORPHENADRINE HYDROCHLORIDE | Synonyms: | 2-Dimethylaminoethyl 2-methylbenzhydryl ether hydrochloride;Ethanamine, N,N-dimethyl-2-[(2-methylphenyl)phenylmethoxy]-, hydrochloride;Ethylamine, N,N-dimethyl-2-((o-methyl-alpha-phenylbenzyl)oxy)-, hydrochloride;Ethylamine, N,N-dimethyl-2-(alpha-(o-tolyl)benzyloxy)-, hydrochloride;Ethylamine, N,N-dimethyl-2-(phenyl-(o-tolyl)methoxy)-, hydrochloride;Mebedrol;Mefenamin hydrochloride;Mephenamin | CAS: | 341-69-5 | MF: | C18H24ClNO | MW: | 305.84 | EINECS: | 206-435-4 | Product Categories: | API | Mol File: | 341-69-5.mol | |
| ORPHENADRINE HYDROCHLORIDE Chemical Properties |
Melting point | 159.0 to 164.0 °C | Boiling point | -195 °C | density | 0.295 g/cm3 | storage temp. | 2-8°C | solubility | Freely soluble in water and in ethanol (96 per cent). | form | neat | color | Crystals | BRN | 3745818 | Stability: | Stable. Incompatible with strong oxidizing agents. | CAS DataBase Reference | 341-69-5(CAS DataBase Reference) | EPA Substance Registry System | Orphenadrine hydrochloride (341-69-5) |
Hazard Codes | Xn | Risk Statements | 22 | Safety Statements | 36 | RIDADR | 3249 | WGK Germany | 3 | RTECS | KR6300000 | HazardClass | 6.1(b) | PackingGroup | III | Toxicity | LD50 oral in rat: 255mg/kg |
| ORPHENADRINE HYDROCHLORIDE Usage And Synthesis |
Chemical Properties | White or almost white, crystalline powder. | Uses | Antihistaminic;H1 antogonist | Definition | ChEBI: A hydrochloride comprising equimolar amounts of ophenadrine and hydrogen chloride. | General Description | Odorless white or almost white crystalline powder. pH (aqueous solution) about 5.5. Bitter numbing taste. | Air & Water Reactions | May be sensitive to prolonged exposure to light and air. Water soluble. | Reactivity Profile | ORPHENADRINE HYDROCHLORIDE is incompatible with strong oxidizers. | Fire Hazard | Flash point data for ORPHENADRINE HYDROCHLORIDE are not available; however, ORPHENADRINE HYDROCHLORIDE is probably combustible. | Biochem/physiol Actions | Muscarinic receptor antagonist; H1 histamine receptor antagonist; muscle relaxant. Orphenadrine has also been reported to inhibit the noradrenergic transporter and to block the NMDA receptor ion channel. | Clinical Use | Anti-muscarinic:
Parkinsonism
Drug induced extra-pyramidal symptoms | Safety Profile | Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Human systemic effects: mydriasis @updlaryd ilation), hallucinations, distorted perceptions, pulse rate increase, intracranial pressure increase. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and HCl | Metabolism | Orphenadrine is almost completely metabolised to at least
8 metabolites in the liver.
It is mainly excreted in the urine as metabolites and small
amounts of unchanged drug |
| ORPHENADRINE HYDROCHLORIDE Preparation Products And Raw materials |
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