Benazepril Hydrochloride EP Impurity A

Benazepril Hydrochloride EP Impurity A is chemically [(3R)-3-[[(1R)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid (as per EP) ; (3R)-3-[[(1R)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid (as per USP). It is also known as Benazepril USP Related Compound A. Benazepril Hydrochloride EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Benazepril Hydrochloride EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Benazepril hydrochloride.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.