This impurity is related to Crizotinib Deschloro 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.
Crizotinib Deschloro Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(R)-3-(1-(2-chloro-3-fluorophenyl)ethoxy)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amineCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Crizotinib Molecular Formula: C21H23ClFN5O
Molecular Weight: 415.9
Storage: Store in a cool, dry place.