This impurity is related to Losartan EP Impurity B 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.
Losartan EP Impurity B is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:p-(o-1H-Tetrazol-5-ylphenyl)benzyl alcoholCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Losartan Molecular Formula: C14H12N4O
Molecular Weight: 252.3
Storage: Store in a cool, dry place.