IUPAC Name: [4-(Dimethylamino)-4-oxobutyl] 2-(4-chlorophenoxy)-2-methylpropanoate
Synonyms: 2-(4-Chlorophenoxy)-2-methylpropanoic Acid 4-(Dimethylamino)-4-oxobutyl Ester ; 4-(Dimethylamino)-4-oxobutyl 2-(4-chlorophenoxy)-2-methylpropanoate ; 4-(Dimethylamino)-4-oxobutyl 2-[(4-chlorophenyl)oxy]-2-methylpropanoate ; Clofibride ;propanoic acid, 2-(4-chlorophenoxy)-2-methyl-, 4-(dimethylamino)-4-oxobutyl ester ; Propionic acid, 2-(4-chlorophenoxy)-2-methyl-, 4-(dimethylamino)-4-oxobutyl ester (9CI)
Molecular Formula of Lipenan (CAS NO.26717-47-5) : C16H22ClNO4
Molecular Weight of Lipenan (CAS NO.26717-47-5) : 327.8032
Molecular Structure of Lipenan (CAS NO.26717-47-5) :
CAS NO: 26717-47-5
Index of Refraction: 1.515
Surface Tension: 39.9 dyne/cm
Density: 1.163 g/cm3
Flash Point: 225.2 °C
Enthalpy of Vaporization: 70.73 kJ/mol
Boiling Point: 448.7 °C at 760 mmHg
Vapour Pressure: 3.04E-08 mmHg at 25°C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 960mg/kg (960mg/kg) | BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) LUNGS, THORAX, OR RESPIRATION: CYANOSIS LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION | Journal Europeen de Toxicologie. Vol. 5, Pg. 239, 1972. |
mouse | LD50 | oral | 1080mg/kg (1080mg/kg) | BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) LUNGS, THORAX, OR RESPIRATION: CYANOSIS LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION | Journal Europeen de Toxicologie. Vol. 5, Pg. 239, 1972. |
rat | LD50 | intraperitoneal | 1175mg/kg (1175mg/kg) | BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) LUNGS, THORAX, OR RESPIRATION: CYANOSIS LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION | Journal Europeen de Toxicologie. Vol. 5, Pg. 239, 1972. |
rat | LD50 | oral | 2485mg/kg (2485mg/kg) | BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) LUNGS, THORAX, OR RESPIRATION: CYANOSIS LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION | Journal Europeen de Toxicologie. Vol. 5, Pg. 239, 1972. |
Moderately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of Cl− and NOx.
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