This impurity is related to Ruxolitinib Impurity 16 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.
Ruxolitinib Impurity 16 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(Z)-2-((S)-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)(cyclopentyl)methyl)-3-(4-(1-((R)-2-cyano-1-cyclopentylethyl)-1H-pyrazol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acrylonitrileCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ruxolitinib Molecular Formula: C35H34N12
Molecular Weight: 622.7
Storage: Store in a cool, dry place.