This impurity is related to Cabazitaxel Impurity 37 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 37 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2-Chloro-1-(2,7-dichloro-9H-fluoren-4-yl)ethan-1-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cabazitaxel Molecular Formula: C15H9Cl3O
Molecular Weight: 311.6
Storage: Store in a cool, dry place.