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ORPHENADRINE HYDROCHLORIDE

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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
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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).
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)
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Safety Information

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
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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

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