This impurity is related to N-Nitroso Binimetinib Impurity 21 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.
N-Nitroso Binimetinib Impurity 21 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,3S,4S,5R,6R)-6-(2-((5-((4-bromo-2-fluorophenyl)amino)-4-fluoro-1-nitroso-1H-benzo[d]imidazole-6-carboxamido)oxy)ethoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Binimetinib Molecular Formula: C22H20BrF2N5O10
Molecular Weight: 632.33
Storage: Store in a cool, dry place.