This impurity is related to Ceftaroline Impurity 7 is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Ceftaroline Impurity 7 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6R,6'R,7R,7'R)-7,7'-(((2Z,2'Z)-2,2'-(((1,3-dihydroxy-1,3-dioxo-1l5,3l5-diphosphoxane-1,3-diyl)bis(azanediyl))bis(1,2,4-thiadiazole-5,3-diyl))bis(2-(ethoxyimino)acetyl))bis(azanediyl))bis(3-((4-(1-methylpyridin-1-ium-4-yl)thiazol-2-yl)thio)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ceftaroline Fosamil Molecular Formula: C44H40N16O15P2S8
Molecular Weight: 1351.3
Storage: Store in a cool, dry place.