5-(1-hydroxy-2-((1-(4-hydroxyphenyl)propan-2-yl)amino)ethyl)benzene-1,3-diol; rel-5-[(1S)-1-Hydroxy-2-[[(1R)-2-(4-hydroxyphenyl)-1-methylethyl]amino]ethyl]-1,3-benzenediol ; (R*,S*)-5-[1-Hydroxy-2-[[2-(4-hydroxyphenyl)-1-methylethyl]amino]ethyl]-1,3-benzenediol ; (R*,S*)-(±)-5-[1-Hydroxy-2-[[2-(4-hydroxyphenyl)-1-methylethyl]amino]ethyl]-1,3-benzenediol
Fenoterol EP Impurity A is a fully characterized chemical compound used as a reference standard of API Fenoterol. The standard offered is compliant with regulatory guidelines. Fenoterol EP 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 - 107878-38-6
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Fenoterol Degradation Impurity A HBr (Mixture of Diastereomers)
M.F.
M.W. 315.37 80.91
CAT# AR-F01310
CAS# NA
