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58-74-2

Supplier Related Products Identification Chemical Properties Hazard Information Safety Data Raw materials And Preparation Products Spectrum Detail

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Identification

Name
PAPAVERINE HYDROCHLORIDE
CAS
58-74-2
Synonyms
S-M-R
Papacon
Papaveri
Robaxapap
Papalease
papaverin
papanerin
Papanerine
PAPAVERINE
Papaverina
AKOS 220-12
PAPAVERINE HCL
Papaverine,99%
Papanerin-HCl [German]
18) META CHLORO BENZALDEHYDE
6,7-dimethoxy-1-veratryl-isoquinolin
6,7-Dimethoxy-1-veratrylisoquinoline
Isoquinoline, 6,7-dimethoxy-1-veratryl-
6,7-DIMETHOXY-1-VERATRYLISOQUINOLINE HCL
6,7-DIMETHOXY-1-VERATRYL-ISOQUINOLINE HYDROCHLORIDE
1-(3,4-DIMETHOXY-BENZYL)-6,7-DIMETHOXY-ISOQUINOLINE
1-((3,4-dimethoxyphenyl)methyl)-6,7-dimethoxy-isoquinolin
1-((3,4-Dimethoxyphenyl)methyl)-6,7-dimethoxyisoquinoline
isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethox
Isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-
1-[(3',4'-DIMETHOXYPHENYL)METHYL]-6,7-DIMETHOXYISOQUINOLINE HCL
EINECS(EC#)
200-502-1
Molecular Formula
C20H22ClNO4
MDL Number
MFCD00012745
Molecular Weight
375.85
MOL File
58-74-2.mol

Chemical Properties

Melting point 
226 °C
density 
d420 1.337
solubility 
H2O: 25 mg/mL

form 
powder

pka
6.4(at 25℃)
color 
white

Merck 
14,7019
BRN 
312930

Hazard Information

Uses
folate metabolic inhibitor, coccidiostat
Uses
muscle relaxant (smooth), cerebral vasodilator
Uses
opium alkaloid
Definition
ChEBI: A benzylisoquinoline alkaloid that is isoquinoline substituted by methoxy groups at positions 6 and 7 and a 3,4-dimethoxybenzyl group at position 1. It has been isolated from Papaver somniferum.

Safety Data

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
22
RIDADR 
UN 1544 6.1/PG 3

WGK Germany 
1

RTECS 
NW8575000


8
HazardClass 
6.1(a)
PackingGroup 
II
Safety Profile
Poison by ingestion, intramuscular, subcutaneous, intradermal, intraperitoneal, and intravenous routes. Human systemic effects: coma, somnolence. Its central nervous system action is about midway between those of morphme and codeine, and large doses do not produce the amount of excitement caused by codeine or the soporific action of morphine. Mutation data reported. A cerebral vasodilator and smooth muscle relaxant. Combustible when exposed to heat or flame. When heated to decomposition it emits toxic fumes of NOx. See also MORPHINE.

Raw materials And Preparation Products

Spectrum Detail