Fosinopril EP Impurity E

Fosinopril EP Impurity E is chemically (2S,4S)-1-[[(R)-[(1S)-2-methyl-1-(propanoyloxy)propoxy](4-phenylbutyl)phosphoryl]acetyl]-4-phenylpyrrolidine-2-carboxylic acid (as per EP) ; (4S)-4-phenyl-1-[(R)-[(S)-1-hydroxy-2-methyl-propoxy](4-phenylbutyl)phospinyl]acetyl-L-proline propionate (ester) (as per USP). It is also known as Phenylfosinopril (EP) ; Fosinopril USP Related Compound E. Fosinopril EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Fosinopril EP Impurity E 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 Fosinopril.

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.