Hexahydroramipril; Ramipril USP Related Compound C; (2S,3aS,6aS)-1-((S)-2-(((S)-4-cyclohexyl-1-ethoxy-1-oxobutan-2-yl)amino)propanoyl)octahydrocyclopenta[b]pyrrole-2-carboxylic acid;Ramipril related compound C;Ramipril related compound C [USP];Ramipril specified impurity C [EP];Ramipril related compound C RS [USP];Cyclohexyl Ramipril Analogue;Cyclopenta(b)pyrrole-2-carboxylic acid, 1-((2S)-2-(((1S)-3-cyclohexyl-1-(ethoxycarbonyl)propyl)amino)-1-oxopropyl)octahydro-, (2S,3aS,6aS)-
Ramipril EP Impurity C is a fully characterized chemical compound used as a reference standard of API Ramipril. The standard offered is compliant with regulatory guidelines. Ramipril EP Impurity C is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 99742-35-5
