This impurity is related to Azilsartan Impurity 41 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 Impurity 41 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(Z)-(Amino(4'-((2-ethoxy-7-(ethoxycarbonyl)-1H-benzo[d]imidazol-1-yl)methyl)-[1,1'-biphenyl]-2-yl)methylene)carbamic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Azilsartan Molecular Formula: C27H26N4O5
Molecular Weight: 486.5
Storage: Store in a cool, dry place.