This impurity is related to Ibrutinib Impurity 22 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.
Ibrutinib Impurity 22 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-N-(1-(1-(3-(4-(4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)propanoyl)piperidin-3-yl)-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)acrylamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ibrutinib Molecular Formula: C50H48N12O4
Molecular Weight: 881
Storage: Store in a cool, dry place.