Cefuroxime EP Impurity H | CAS 947723-87-7 - Request Quote

Cefuroxime EP Impurity H is chemically (5aR,6R)-6-[[(Z)-(Furan-2-yl)(methoxyimino)acetyl]amino]-5a,6-dihydro-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazine-1,7(4H)-dione (as per EP) ; (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 (as per USP). It is also known as Cefuroxime Axetil EP Impurity E ; Cefuroxime Lactone (USP). Cefuroxime EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Cefuroxime EP Impurity H 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 Cefuroxime.

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.