This impurity is related to Deferoxamine Impurity 7 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.
Deferoxamine Impurity 7 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N1-(8,19-dihydroxy-1-((4-isothiocyanatophenyl)amino)-9,12,20,23-tetraoxo-1-thioxo-2,8,13,19,24-pentaazanonacosan-29-yl)-N1-hydroxy-N4-(5-(N-hydroxyacetamido)pentyl)succinamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Deferoxamine Molecular Formula: C42H68N10O11S2
Molecular Weight: 953.2
Storage: Store in a cool, dry place.