logo
REACH OUT TO US +91 82830 85118 +91 91157 96473 contact@gspharma.tech


Impurity of Candesartan Cilexetil
Candesartan EP Impurity E
Impurity
GS.08.CAD.05_1779711405.png
Download COA
Product Name Candesartan EP Impurity E
Product Category Impurities, Intermediates
Sub-Category Heterocycles, Pharmaceutical Standards, Fine Chemicals, Aromatics
CAS No 914613-35-7
Catalog Number GS.08.CAD.05
Chemical Name/Synonyms 1H-1-Ethyl Candesartan Cilexetil ; Candesartan Cilexetil N1-Ethyl Analog ; 1H-N1-Ethyl Candesartan Cilexetil ; 2-Ethoxy-1-[[2'-[1-ethyl-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carboxylic acid 1-[[(cyclohexyloxy) carbonyl]oxy]ethyl ester
Molecular Weight 638.71
Molecular Formula C35H38N6O6
Purity NLT 95%
Appearance White Solid
Solubility methanol, chloroform, methylene chloride
Applications Candesartan Cilexetil is primarily utilized in pharmaceutical research as an analytical reference standard. It is mainly used to test drug purity, identify specific byproducts, and quantify related substance profiles during quality control.
Inventory Status Ready Stock     Please as a distributor to view package sizes and prices