(S)-1-((S)-6-((S)-2-(((S)-6-amino-1-((S)-2-carboxypyrrolidin-1-yl)-1-oxohexan-2-yl)amino)-4-phenylbutanamido)-2-(((S)-1-carboxy-3-phenylpropyl)amino)hexanoyl)pyrrolidine-2-carboxylicacid;(S)-Lisinopril Dimer
Lisinopril EP Impurity G (Dimer Impurity) is a fully characterized chemical compound used as a reference standard of API Lisinopril. The standard offered is compliant with regulatory guidelines. Lisinopril EP Impurity G (Dimer Impurity) 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 - 1356839-89-8
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