3'-N-[[4-(Acetylamino)phenyl]sulfonyl]-3'-N-demethyl Azithromycin; (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-[[3-[[[4-(Acetylamino)phenyl]sulfonyl]methylamino]-3,4,6-trideoxy-?-D-xylo-hexopyranosyl]oxy]-13-[(2,6-dideoxy-3-C-methyl-3-O-methyl-?-L-ribo-hexopyranosyl)oxy]-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-azacyclopentadecan-15-one; USP Azithromycin Related Impurity H
Azithromycin EP Impurity H is a fully characterized chemical compound used as a reference standard of API Azithromycin. The standard offered is compliant with regulatory guidelines. Azithromycin EP Impurity H 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 - 612069-30-4
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