Product Name

Iodoxamate meglumine Chemical Properties

IUPAC Name: 3-[3-[2-[2-[2-[3-[(3-Carboxy-2,4,6-triiodo-phenyl)amino]-3-oxo-propoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-2,4,6-triiodo-benzoic acid; (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol
Synonyms of Iodoxamate meglumine (CAS NO.696-33-3) : 3,3'-(Ethylenebis(oxyethyleneoxyethylenecarbonylimino))bis(2,4,6-triiodobenzoic acid) compound with 1-deoxy-1-(methylamino)-D-glucitol (1:2) ; Bis(1-deoxy-1-(methylamino)-D-glucitol) 3,3'-((1,16-dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino)bis(2,4,6-triiodobenzoate) ; bis[1-Deoxy-1-(methylamino)-D-glucitol] 3,3'-[(1,16-dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino]bis[2,4,6-triiodobenzoate]
CAS NO:696-33-3
Molecular Formula:C26H26I6N2O10.2C7H17NO5
Molecular Weight :1678.346
Molecular Structure :
EINECS: 257-398-6
Flash Point: 801 °C
Enthalpy of Vaporization: 222.99 kJ/mol
Boiling Point: 1400.8 °C at 760 mmHg
Vapour Pressure: 0 mmHg at 25°C

Iodoxamate meglumine Uses

 Iodoxamate meglumine (CAS NO.696-33-3) is used as  intermediate in organic synthesis.

Iodoxamate meglumine Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 intravenous 4850mg/kg (4850mg/kg)   Farmaco, Edizione Scientifica. Vol. 28, Pg. 996, 1973.
mouse LD50 intravenous 5300mg/kg (5300mg/kg)   Drugs in Japan Vol. 6, Pg. 871, 1982.
rabbit LD50 parenteral 5398mg/kg (5398mg/kg)   Farmaco, Edizione Scientifica. Vol. 28, Pg. 1011, 1973.
rat LD50 intravenous 4500mg/kg (4500mg/kg)   Drugs in Japan Vol. 6, Pg. 871, 1982.
rat LD50 parenteral 2928mg/kg (2928mg/kg)   Farmaco, Edizione Scientifica. Vol. 28, Pg. 1011, 1973.

 

Iodoxamate meglumine Safety Profile

Moderately toxic by parenteral route. When Iodoxamate meglumine (CAS NO.696-33-3) is heated to decomposition ,it emits toxic fumes of I and NOx.

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