Candesartan Cilexetil EP Impurity B | CAS 869631-11-8 - Solicitar cotización

Candesartan Cilexetil EP Impurity B is chemically (1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-oxo-3-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-2,3-dihydro-1H-benzimidazole-4-carboxylate (as per EP) ; 1-{[(Cyclohexyloxy)carbonyl]oxy}ethyl 3-({2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl}methyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carboxylate (as per USP). It is also known as Candesartan Cilexetil USP Related Compound B ; Candesartan Cilexetil O-Desethyl Analog ; Candesartan Ketone Cilexetil. Candesartan Cilexetil EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Candesartan Cilexetil EP Impurity B can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Candesartan.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.