(1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 3-[[2′-(1-ethyl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-2-oxo-2,3-dihydro-1H-benzimidazole-4-carboxylate (as per EP); Candesartan Cilexetil N1-Ethyl Amide ; Candesartan Cilexetil O-Desethyl N1-Ethyl Impurity ; 2-Desethoxy-2-Hydroxy-1H-N1-Ethyl Candesartan Cilexeti
Candesartan Cilexetil EP Impurity C is a fully characterized chemical compound used as a reference standard of API Candesartan. The standard offered is compliant with regulatory guidelines. Candesartan Cilexetil EP Impurity C is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 1185255-99-5
