This impurity is related to Ceritinib Impurity 12 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.
Ceritinib Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2,5-Dichloro-N-(2-(ethylsulfonyl)phenyl)pyrimidin-4-amineCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ceritinib Molecular Formula: C12H11Cl2N3O2S
Molecular Weight: 332.2
Storage: Store in a cool, dry place.