This impurity is related to Ezetimibe Impurity 21 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.
Ezetimibe Impurity 21 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-3-((2R, 5R)-5-((tert-butyldimethylsilyl)oxy)-2-((S)-(4-((tert-butyldimethylsilyl)oxy)phenyl)((4-fluorophenyl)amino)methyl)-5-(4-fluorophenyl)pentanoyl)-4-phenyloxazolidin-2-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ezetimibe Molecular Formula: C45H58F2N2O5Si2
Molecular Weight: 801.13
Storage: Store in a cool, dry place.