| Cefotaxime Sodium EP Impurity E is chemically (5aR,6R)-6-[[(2Z)-2-(2-Aminothiazol-4-yl)-2-(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). It is also known as Deacetylcefotaxime lactone (EP). Cefotaxime Sodium EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Cefotaxime Sodium EP Impurity E 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 Cefotaxime Sodium. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use. |