This impurity is related to Ceftaroline Impurity 13 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 13 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6R,7R)-7-(2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetamido)-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-carboxylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ceftaroline Fosamil Molecular Formula: C22H20N8O5S4
Molecular Weight: 604.7
Storage: Store in a cool, dry place.