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98459-16-6

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Basic Information
CAS No.: 98459-16-6
Name: centphenaquin
Molecular Structure:
Molecular Structure of 98459-16-6 (centphenaquin)
Formula: C24H27 N3 . 2 Cl H
Molecular Weight: 429.41
Synonyms: 6H-Cyclohepta[b]quinoline,7,8,9,10-tetrahydro-11-(4-phenyl-1-piperazinyl)-, dihydrochloride (9CI);Centphenaquin
Density: g/cm3
Boiling Point: 581.1°Cat760mmHg
Flash Point: 305.2°C
Safety: Poison by intravenous route. Moderately toxic by intraperitoneal route. When heated to decomposition it emits toxic fumes of NOx and HCl.
PSA: 19.37000
LogP: 6.56430
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Chemistry

Chemistry informtion about Centphenaquin (CAS NO.98459-16-6) is:
IUPAC Name: 11-(4-Phenylpiperazin-1-Yl)-7,8,9,10-Tetrahydro-6h-Cyclohepta[B]Quinoline Dihydrochloride
Synonyms: Centphenaquin
MF: C24H29Cl2N3
MW: 430.413160 g/mol 
Flash Point: 305.2 °C
Boiling Point: 581.1 °C at 760 mmHg
Vapour Pressure: 1.71E-13 mmHg at 25°C 
Enthalpy of Vaporization: 86.9 kJ/mol
Following is the molecular structure of Centphenaquin (CAS NO.98459-16-6) is:

Toxicity Data With Reference

Toxic information about Centphenaquin (CAS NO.98459-16-6) is:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 494mg/kg (494mg/kg) behavioral: convulsions or effect on seizure threshold lungs, thorax, or respiration: cyanosis Indian Journal of Experimental Biology. Vol. 23, Pg. 214, 1985.
mouse LD50 intravenous 56mg/kg (56mg/kg) behavioral: convulsions or effect on seizure threshold lungs, thorax, or respiration: cyanosis Indian Journal of Experimental Biology. Vol. 23, Pg. 214, 1985.
mouse LD50 subcutaneous > 2gm/kg (2000mg/kg)   Indian Journal of Experimental Biology. Vol. 23, Pg. 214, 1985.
rat LD50 intraperitoneal 493mg/kg (493mg/kg) behavioral: convulsions or effect on seizure threshold lungs, thorax, or respiration: cyanosis Indian Journal of Experimental Biology. Vol. 23, Pg. 214, 1985.

Safety Profile

Poison by intravenous route. Moderately toxic by intraperitoneal route. When heated to decomposition it emits toxic fumes of NOx and HCl.