This impurity is related to Ifosfamide EP Impurity A 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.
Ifosfamide EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:3-((2-Chloroethyl)amino)propyl Dihydrogen Phosphate (Ester)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ifosfamide Molecular Formula: C5H13ClNO4P
Molecular Weight: 217.6
Storage: Store in a cool, dry place.