cis-5-[(2RS)-3-[(1,1-dimethylethyl)amino]-2-hydroxypropoxy]-8-iodo-1,2,3,4-tetrahydronaphtalene-2,3-diol
Nadolol EP Impurity E is a fully characterized chemical compound used as a reference standard of API Nadolol. The standard offered is compliant with regulatory guidelines. Nadolol 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 -
