This impurity is related to Olmesartan Anhydro Acid 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.
Olmesartan Anhydro Acid Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:4-(Prop-1-en-2-yl)-2-propyl-1-[[2?-(1H-tetrazol-5-yl) biphenyl-4-yl] methyl]-1Himidazole-5-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Olmesartan Molecular Formula: C24H24N6O2
Molecular Weight: 428.5
Storage: Store in a cool, dry place.