Basic Information | Post buying leads | Suppliers |
Name |
1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride |
EINECS | N/A |
CAS No. | 2192-21-4 | Density | 1.043g/cm3 |
PSA | 29.54000 | LogP | 5.02470 |
Solubility | N/A | Melting Point |
N/A |
Formula | C21H27 N O2 . Cl H | Boiling Point | 464.2°Cat760mmHg |
Molecular Weight | 361.95 | Flash Point | 234.5°C |
Transport Information | N/A | Appearance | N/A |
Safety | Poison by ingestion and intravenous routes. When heated to decomposition it emits very toxic fumes of NOx and HCl. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Propiophenone,2'-[2-(diethylamino)ethoxy]-3-phenyl-, hydrochloride (6CI,7CI,8CI); Asmedol;Baxacor; Corodilan; Dialicor; Etafenone hydrochloride; Heptaphenone;Pagano-Cor; Relicor; o-(b-Diethylaminoethoxy)phenylpropiophenone hydrochloride |
IUPAC Name :1-[2-(2-Diethylaminoethyloxy)phenyl]-3-phenylpropan-1-one hydrochloride
Synonyms: 1-Propanone, 1-(2-(2-(diethylamino)ethoxy)phenyl)-3-phenyl-, hydrochloride (9CI) ; 1-Propanone, 1-[2-[2- (diethylamino)ethoxy]phenyl]-3-phenyl-, hydrochloride ; Etafenone hydrochloride (JAN) ; Propiophenone, 2'-[2- (diethylamino)ethoxy]-3-phenyl-, hydrochloride
CAS NO:2192-21-4
Molecular Formula of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) : C21H28ClNO2
Molecular Weight of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) : 361.90552
Molecular Structure of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) :
EINECS: 218-587-9
Flash Point: 234.5 °C
Enthalpy of Vaporization: 72.56 kJ/mol
Boiling Point: 464.2 °C at 760 mmHg
Vapour Pressure: 8.53E-09 mmHg at 25°C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
dog | LD50 | oral | 50mg/kg (50mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969. |
mouse | LD50 | intraperitoneal | 90mg/kg (90mg/kg) | Drugs in Japan Vol. -, Pg. 180, 1990. | |
mouse | LD50 | intravenous | 28mg/kg (28mg/kg) | Pharmaceutical Chemistry Journal Vol. 23, Pg. 966, 1989. | |
mouse | LD50 | oral | 352mg/kg (352mg/kg) | Drugs in Japan Vol. 6, Pg. 109, 1982. | |
mouse | LD50 | subcutaneous | 234mg/kg (234mg/kg) | Pharmaceutical Chemistry Journal Vol. 21, Pg. 646, 1987. | |
rat | LD50 | intraperitoneal | 66mg/kg (66mg/kg) | Drugs in Japan Vol. -, Pg. 180, 1990. | |
rat | LD50 | intravenous | 20800ug/kg (20.8mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969. |
rat | LD50 | oral | 716mg/kg (716mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969. |
rat | LD50 | subcutaneous | 1900mg/kg (1900mg/kg) | Drugs in Japan Vol. -, Pg. 180, 1990. |
Poison by ingestion and intravenous routes. When heated to decomposition it emits very toxic fumes of NOx and HCl.