This impurity is related to Gilteritinib N-Oxide 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.
       
      
        Gilteritinib N-Oxide Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
       
      
        Chemical Name:1-(1-(4-((3-Carbamoyl-5-ethyl-6-((tetrahydro-2H-pyran-4-yl)amino)pyrazin-2-yl)amino)-2-methoxyphenyl)piperidin-4-yl)-4-methylpiperazine 1-oxideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Gilteritinib Molecular Formula: C29H44N8O4
Molecular Weight: 568.7
Storage: Store in a cool, dry place.