ORPHENADRINE HYDROCHLORIDE

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 Structure
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 Reference341-69-5(CAS DataBase Reference)
EPA Substance Registry SystemOrphenadrine hydrochloride (341-69-5)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 36
RIDADR 3249
WGK Germany 3
RTECS KR6300000
HazardClass 6.1(b)
PackingGroup III
ToxicityLD50 oral in rat: 255mg/kg
MSDS Information
ORPHENADRINE HYDROCHLORIDE Usage And Synthesis
Chemical PropertiesWhite or almost white, crystalline powder.
UsesAntihistaminic;H1 antogonist
DefinitionChEBI: A hydrochloride comprising equimolar amounts of ophenadrine and hydrogen chloride.
General DescriptionOdorless white or almost white crystalline powder. pH (aqueous solution) about 5.5. Bitter numbing taste.
Air & Water ReactionsMay be sensitive to prolonged exposure to light and air. Water soluble.
Reactivity ProfileORPHENADRINE HYDROCHLORIDE is incompatible with strong oxidizers.
Fire HazardFlash point data for ORPHENADRINE HYDROCHLORIDE are not available; however, ORPHENADRINE HYDROCHLORIDE is probably combustible.
Biochem/physiol ActionsMuscarinic 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 UseAnti-muscarinic:
Parkinsonism
Drug induced extra-pyramidal symptoms

Safety ProfilePoison 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
MetabolismOrphenadrine 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
Venlafaxine hydrochloride Diphenhydramine Levofloxacin hydrochloride Betahistine dihydrochloride Tropisetron hydrochloride Orphenadrine 2-(BENZYLOXY)-ETHYLAMINE tofenacin 2-(DIMETHYLAMINO)-ETHANOL HYDROCHLORIDE Ethylamine hydrochloride ORPHENADRINE HYDROCHLORIDE 2-Methylbenzhydrol Diphenhydramine Hydrochloride 2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE ORPHENADRINE HYDROCHLORIDE IMP. A (EP): (RS)-(2-METHYLPHENYL)PHENYLMETHANOL (2-METHYLBENZHYDROL) 2-(DIPHENYLMETHOXY)-N-METHYLETHYLAMINE tofenacin hydrochloride

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