This impurity is related to Zanubrutinib 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.
Zanubrutinib Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(7S)-7-(1-acryloylpiperidin-4-yl)-4-(3-(4-((7S)-3-carbamoyl-2-(4-phenoxyphenyl)-5,6,7,7a-tetrahydro-4H-pyrrolo[3,2-b]pyridin-7-yl)piperidin-1-yl)-3-oxopropyl)-2-(4-phenoxyphenyl)-5,6,7,7a-tetrahydro-4H-pyrrolo[3,2-b]pyridine-3-carboxamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Zanubrutinib Molecular Formula: C56H60N8O6
Molecular Weight: 941.1
Storage: Store in a cool, dry place.