This impurity is related to Docetaxel 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.
Docetaxel EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:5?,20-Epoxy-1,7?-dihydroxy-9-oxotax-11-ene-2?,4,10?,13?-tetrayl 4,10-diacetate 2-benzoate 13-[(2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenyl propanoate]Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Docetaxel Molecular Formula: C47H51NO14
Molecular Weight: 853.9
Storage: Store in a cool, dry place.