NALORPHINE
- Product Name
- 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
- Formula Weight
- 311.37
- MOL File
- 62-67-9.mol
NALORPHINE Property
- 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)
Safety
- Hazardous Substances Data
- 62-67-9(Hazardous Substances Data)
- DEA Controlled Substances
- CSCN: 9319
CAS SCH: Ⅰ
NARC: Y
NALORPHINE Chemical Properties,Usage,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