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NALORPHINE HYDROCHLORIDE

NALORPHINE HYDROCHLORIDE Basic information
Product Name: NALORPHINE HYDROCHLORIDE
Synonyms:6-alpha-diol,17-allyl-7,8-didehydro-4,5-alpha-epoxy-morphinan-hydrochlorid;allylmorphinehydrochloride;miromorfalil;nalinehydrochloride;n-allyl-2,12-dihydroxy-1,11-epoxymorphinene-13hydrochloride;n-allylnormorphinehydrochloride;n-allyl-normorphinhydrochloride;NALORPHINE HYDROCHLORIDE CIII (250 MG)
CAS:57-29-4
MF:C19H21NO3.ClH
MW:347.84
EINECS:200-321-8
Product Categories:Pharmaceuticals;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals
Mol File:57-29-4.mol
	NALORPHINE HYDROCHLORIDE Structure
NALORPHINE HYDROCHLORIDE Chemical Properties
Melting point 260-263°
Fp 11 °C
storage temp. 2-8°C
solubility H2O: slightly soluble
form solid
color white
Safety Information
Hazard Codes Xn,T,F
Risk Statements 22-39/23/24/25-23/24/25-11
Safety Statements 36/37/39-45-36/37-16-7
RIDADR UN 1230 3/PG 2
WGK Germany 3
RTECS QC7710000
HS Code 2939190000
ToxicityLD50 s.c. in rats: 1460 mg/kg (Goldenthal)
MSDS Information
NALORPHINE HYDROCHLORIDE Usage And Synthesis
OriginatorNalline,MSD,US,1952
UsesNarcotic antagonist. Controlled substance.
Manufacturing Process6 grams of normorphine, 2.7 grams of allyl bromide, 2.65 grams of sodium bicarbonate, and 75 cc of methanol were mixed together, and the resulting mixture was heated under reflux with stirring for a period of about 5 1/2 hours. The reaction mixture was evaporated to dryness in vacuo, the residual material was extracted with 60 cc of boiling chloroform, 0.5 gram of activated charcoal was added, and the resulting mixture was filtered through a layer of diatomaceous silica. The filter cake was washed with four 10 cc portions of boiling chloroform, and the chloroform filtrate and washings were combined and evaporated to dryness in vacuo. The residual material was triturated with 25 cc of anhydrous ether until crystalline, the ethereal mixture was cooled, maintained at a temperature of 3°C overnight, filtered, and the crystalline mixture was washed with three 10 cc portions of ice-cold ether. The resulting crystalline product was dried to give 6.0 grams of N-allylnormorphine, yield approximately 87% of theory, according to US Patent 2,891,954.
Therapeutic FunctionNarcotic antagonist
NALORPHINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materialsNORMORPHINE-->Allyl bromide-->Sodium bicarbonate
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