Azithromycin EP Impurity L | CAS 90503-06-3 - Solicitar cotización

Azithromycin EP Impurity L is chemically Azithromycin 3'-N-Oxide (as per EP) ; (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[(2,6-Dideoxy-3-C-methyl-3-O-methyl-α-l-ribo-hexopyranosyl)oxy]-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14-heptamethyl-11-[[3,4,6-trideoxy-3-(dimethylazinoyl)-β-d-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one (as per USP). It is also known as Azithromycin N-Oxide (USP). Azithromycin EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Azithromycin EP Impurity L can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Azithromycin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.