7-bromo-5-(3-(tert-butylamino)-2-hydroxypropoxy)-3,4-dihydroquinolin-2(1H)-one
Carteolol EP Impurity I is a fully characterized chemical compound used as a reference standard of API Carteolol. The standard offered is compliant with regulatory guidelines. Carteolol EP Impurity I 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 -