Olmesartan Medoxomil EP Impurity D | CAS 1020157-01-0 - Request Quote

Olmesartan Medoxomil EP Impurity D is chemically (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[[2′-[(2-triphenylmethyl)-2H-tetrazol-5-yl]biphenyl-4-yl]methyl]-1H-imidazole-5-carboxylate (as per EP) ; (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(2-hydroxypropan-2-yl)-2-propyl-1-{[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylate (as per USP). It is also known as Olmesartan EP Impurity D ; Olmesartan medoxomil N-alkyl impurity (USP) ; N2-Trityl Olmesartan Medoxomil. Olmesartan Medoxomil EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Olmesartan Medoxomil EP Impurity D 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 Olmesartan.

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.