This impurity is related to Cabazitaxel Oxazolidine 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.
Cabazitaxel Oxazolidine Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name: 5-((2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-Acetoxy-12-(benzoyloxy)-11-hydroxy-4,6-dimethoxy-4a,8,13,13-tetramethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxet-9-yl) 3-(tert-butyl) (4S,5R)-2,2-dimethyl-4-phenyloxazolidine-3,5-dicarboxylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cabazitaxel Molecular Formula: C48H61NO14
Molecular Weight: 876
Storage: Store in a cool, dry place.