This impurity is related to Celiprolol Hydrochloride EP Impurity I 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.
Celiprolol Hydrochloride EP Impurity I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N-Acetyl-N-(4-ethoxyphenyl)-N?,N?-diethylureaCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Celiprolol Molecular Formula: C15H22N2O3
Molecular Weight: 278.4
Storage: Store in a cool, dry place.