- Synonyms(R)-1-[N2-(1-Carboxy-3-phenylpropyl)-L-lysyl]L-proline Sodium;N2-[(1R)-1-Carboxy-3-phenylpropyl)-L-lysyl]L-proline Sodium;(R)-Lisinopril Sodium Salt
- Description
(R)-1-[N2-(1-Carboxy-3-phenylpropyl)-L-lysyl]L-proline Sodium;N2-[(1R)-1-Carboxy-3-phenylpropyl)-L-lysyl]L-proline Sodium;(R)-Lisinopril Sodium Salt
Lisinopril EP Impurity E is a fully characterized chemical compound used as a reference standard of API Lumacaftor. The standard offered is compliant with regulatory guidelines. Lisinopril EP Impurity E 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 - NA
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Lisinopril Impurity H (Dimer Impurity, Mixture of Diastereomers)

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N-(1-Carboxy-3-phenylpropyl)-S-lisinopril Trisodium Salt (Mixture of diastereomers)

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