(2S,2'S)-diethyl 2,2'-((2R,5S)-2,5-dimethyl-3,6-dioxopiperazine-1,4-diyl)bis(4-phenylbutanoate); (?1S,?4S,2S,5S)-2,5-Dimethyl-3,6-dioxo-?1,?4-bis(2-phenylethyl)-1,4-piperazinediacetic Acid 1,4-Diethyl Ester;[2S-[1(R*),2?,4(R*),5?]]-2,5-Dimethyl-3,6-dioxo-?,?'-bis(2-phenylethyl)-1,4-piperazinediacetic Acid Diethyl Ester
Ramipril EP Impurity O 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 O 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 - 151387-05-2
