This impurity is related to Azilsartan Medoxomil Dimer Impurity is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Azilsartan Medoxomil Dimer Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 2-ethoxy-1-((2'-(5-(2-ethoxy-1-((2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazol-7-yl)-1,2,4-oxadiazol-3-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-carboxylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Azilsartan Medoxomil Molecular Formula: C54H42N8O10
Molecular Weight: 963
Storage: Store in a cool, dry place.