This impurity is related to Sultamicillin EP Impurity F 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.
Sultamicillin EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(((2S,5R,6R)-6-((R)-2-((2S,5R,6R)-6-((R)-2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxamido)-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl)oxy)methyl (2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Sultamicillin Molecular Formula: C41H47N7O12S3
Molecular Weight: 926
Storage: Store in a cool, dry place.