This impurity is related to Fosinopril EP Impurity F 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.
Fosinopril EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,4S)-4-Cyclohexyl-1-[[(R)-(4-phenylbutyl)[(1S)-1-(1- oxopropoxy)propoxy]phosphoryl]acetyl]pyrrolidine-2carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Fosinopril Molecular Formula: C29H44NO7P
Molecular Weight: 549.6
Storage: Store in a cool, dry place.