This impurity is related to Bacampicillin EP Impurity E 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.
Bacampicillin EP Impurity E is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(4S)-2-(3,6-Dioxo-5-phenylpiperazin-2-yl)-5,5-dimethylthiazolidine-4-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Bacampicillin Molecular Formula: C16H19N3O4S
Molecular Weight: 349.4
Storage: Store in a cool, dry place.