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Impurity of Candesartan Cilexetil
Candesartan EP Impurity A / Candesartan Cilexetil Related Compound A (USP)
Impurity
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Product Name Candesartan EP Impurity A / Candesartan Cilexetil Related Compound A (USP)
Product Category Intermediates
Sub-Category Heterocycles, Pharmaceutical Standards, Bases and Related Reagents, Nucleotides, Fine Chemicals, Aromatics
CAS No 139481-58-6
Catalog Number GS.08.CAD.01
Chemical Name/Synonyms Candesartan Ethyl Ester ; 2-Ethoxy-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carboxylic Acid Ethyl Ester ; Ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)-4-biphenylyl] methyl]-1H-benzimidazole-7-carboxylate
Molecular Weight 468.51
Molecular Formula C26H24N6O3
Purity NLT 96%
Appearance white solid powder.
Solubility water, methanol, dimethyl sulfoxide
Applications Candesartan cilexetil is an angiotensin II receptor blocker (ARB) used primarily to treat hypertension (high blood pressure) and heart failure
Inventory Status Ready Stock     Please as a distributor to view package sizes and prices