1-(4-(2-hydroxy-3-((2-(2-methoxyphenoxy)ethyl)amino)propoxy)-9H-carbazol-9-yl)-3-((2-(2-methoxyphenoxy)ethyl)amino)propan-2-ol; N-2-Hydroxy-3-[[2-(methoxyphenoxy)ethyl]amine Carvedilol; Carvedilol USP Related Compound A; Carvedilol EP Impurity A
Carvedilol Impurity A is a fully characterized chemical compound used as a reference standard of API Carvedilol. The standard offered is compliant with regulatory guidelines. Carvedilol Impurity A 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 - 1198090-73-1
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Carvedilol EP Impurity B (Mixture of Diastereomers)
M.F.
M.W. 645.76
CAT# AR-C01545
CAS# 918903-20-5
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