This impurity is related to Olutasidenib Impurity 2 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.
Olutasidenib Impurity 2 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-5-((1-(6-Chloro-7-fluoro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrileCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Olutasidenib Molecular Formula:
Molecular Weight: C18H14ClFN4O2
Storage: Store in a cool, dry place.