(1RS)-1-[(2RS)-3,4-dihydro-2H-1-Benzopyran-2-yl]-2-[[(2RS)-2-[(2SR)-6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl]-2-hydroxyethyl]amino]ethan-1-ol; 1-(chroman-2-yl)-2-((2-(6-fluorochroman-2-yl)-2-hydroxyethyl)amino) ethan-1-ol
Nebivolol EP Impurity A (Desfluoro Nebivolol (Mixture of Diastereomers)) is a fully characterized chemical compound used as a reference standard of API Nebivolo. The standard offered is compliant with regulatory guidelines. Nebivolol EP Impurity A (Desfluoro Nebivolol (Mixture of Diastereomers)) 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 - 1416402-13-5