This impurity is related to Capivasertib 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.
Capivasertib Impurity 21 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:3-Amino-3-(4-chlorophenyl)propan-1-olCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Capivasertib Molecular Formula: C9H12ClNO
Molecular Weight: 185.7
Storage: Store in a cool, dry place.