ChemicalBook >> CAS DataBase List >>NALORPHINE

NALORPHINE

CAS No.
62-67-9
Chemical Name:
NALORPHINE
Synonyms
NANM;NANMr;Nallin;Norfin;Anarcon;Antofin;Nalline;Antorfin;Letidron;Antorphin
CBNumber:
CB5366633
Molecular Formula:
C19H21NO3
Molecular Weight:
311.37
MDL Number:
MFCD00867731
MOL File:
62-67-9.mol
Last updated:2023-05-29 13:57:48

NALORPHINE Properties

Melting point 208-209° (not 92-93° as first given by McCawley)
alpha D25 -155.3° (c = 3 in methanol)
Boiling point 451.42°C (rough estimate)
Density 1.1699 (rough estimate)
refractive index 1.5000 (estimate)
pka pKa 7.73(H2O,t =20,I<0.01) (Uncertain)
FDA UNII U59WB2WRY2
ATC code V03AB02

SAFETY

Risk and Safety Statements

DEA Controlled Substances CSCN: 9319
CAS SCH: Ⅰ
NARC: Y

NALORPHINE Chemical Properties,Uses,Production

Originator

Nalline,MSD,US,1952

Uses

Biochemical research tool for studying the mechanism of narcotic action; also as an antidote for acute morphine poisoning.

Definition

The allyl (–CH2–CH=CH2) derivative of morphine. It is able to “antagonize” or neutralize most of the effects of narcotic drugs (morphine, codeine) but not those of other types of depressants.

Manufacturing Process

6 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 Function

Narcotic antagonist

NALORPHINE Preparation Products And Raw materials

Raw materials

Preparation Products

7,8-didehydro-4,5-epoxy-17-(2-propenyl)-,(5alpha,6alpha)-morphinan-6-diol 7,8-didehydro-4,5-epoxy-17-(2-propenyl)morphinan-3,6-diol Acetorfin Acetorphine Allorphine Anarcon Anthorphine Antofin Antorfin Antorphin Antorphine deacode9400 Lethidrome Lethidrone Letidron lithidron Lithidrone Morphinan-3,6alpha-diol, 17-allyl-7,8-didehydro-4,5alpha-epoxy- Morphinan-3,6-diol, 7,8-didehydro-4,5-epoxy-17-(2-propenyl)-, (5alpha,6alpha)- Nallin Nalline N-Allyl-7,8-dehydro-4,5-epoxy-3,6-dihydroxymorphinan N-Allyl-N-desmethylmorphine N-Allylnormorphine Nalorfina Nalorphin Nalorphinium Nalorrphine NANM NANMr Norfin Normorphine, N-allyl- NALORPHINE NALORPHINE,1.0MG/MLINMETHANOL 17-Allyl-7,8-didehydro-4,5alpha-epoxymorphinan-3,6alpha-diol 17-allyl-7,8-didehydro-4,5-alpha-epoxy-morphinan-6-alpha-diol Morphinan-3,6-diol, 7,8-didehydro-4,5-epoxy-17-(2-propen-1-yl)-, (5α,6α)- NALORPHINE USP/EP/BP 62-67-9