This impurity is related to Ubrogepant Impurity 12 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.
Ubrogepant Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-3-(((3S,5S,6R)-6-methyl-2-oxo-5-phenyl-1-(2,2,2-trifluoroethyl)piperidin-3-yl)carbamoyl)-2'-oxo-1',2',5,7-tetrahydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridine] 1-oxideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ubrogepant Molecular Formula: C29H26F3N5O4
Molecular Weight: 565.6
Storage: Store in a cool, dry place.