This impurity is related to Cabazitaxel Impurity 17 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 Impurity 17 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-Acetoxy-9,11-dihydroxy-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-12-yl (Z)-pent-3-enoateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cabazitaxel Molecular Formula: C29H42O10
Molecular Weight: 550.7
Storage: Store in a cool, dry place.