This impurity is related to Ramipril 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.
Ramipril EP Impurity I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,3aS,6aS)-1-(((S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl)-D-alanyl)octahydrocyclopenta[b]pyrrole-2-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ramipril Molecular Formula: C23H32N2O5
Molecular Weight: 416.5
Storage: Store in a cool, dry place.