(1R,2R,3R,6R,7S,8S,9R,10R,12R,13S)-9-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-3-ethyl-2,10-dihydroxy-7-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-2,6,8,10,12,15,15,17-octamethyl-4,16-dioxa-14-azabicyclo[11.3.1]heptadecan-5-one
Dirithromycin EP Impurity E is a fully characterized chemical compound used as a reference standard of API Dirithromycin. The standard offered is compliant with regulatory guidelines. Dirithromycin 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 -
