(Z)-N-((5aR,6R)-1,7-dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl)-2-(furan-2-yl)-2-(methoxyimino)acetamide;Cefuroximine Impurity E (EP); Cefuroxime Sodium EP Impurity H(Cefuroxime Axetil EP Impurity E);(?Z)-?-(Methoxyimino)-N-[(5aR,6R)-1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-furanacetamide
Cefuroxime Axetil EP Impurity E is a fully characterized chemical compound used as a reference standard of API Cefuroxime. The standard offered is compliant with regulatory guidelines. Cefuroxime Axetil 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 - 947723-87-7
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