This impurity is related to Losartan EP Impurity J 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 J is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:[2-Butyl-4-chloro-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-imidazol-5-yl]methyl acetateCountry of Origin: India Product Category: API NAME: Molecular Formula: C24H25ClN6O2
Molecular Weight: 464.947
Storage: Store in a cool, dry place.