(2S,2'S)-1,1'-((2S,2'S)-3,3'-(propane-2,2-diylbis(sulfanediyl))bis(2-methylpropanoyl))bis(pyrrolidine-2-carboxylic acid); 1,1?-[Propane-2,2-diylbis[sulfanediyl[(2S)-2-methyl-1-oxopropane-3,1-diyl]]]bis[(2S)-pyrrolidine-2-carboxylic]acid
Captopril EP Impurity O is a fully characterized chemical compound used as a reference standard of API Captopril. The standard offered is compliant with regulatory guidelines. Captopril 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 -
