This impurity is related to Gentamicin Impurity 13 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.
Gentamicin Impurity 13 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N-((2R,3R,4S,5R)-2-(((1S,2R,3S,4S,6S)-4,6-Diamino-3-(((2S,3S,6S)-3-amino-6-((S)-1-(methylamino)ethyl)tetrahydro-2H-pyran-2-yl)oxy)-2-hydroxycyclohexyl)oxy)-3,5-dihydroxy-5-methyltetrahydro-2H-pyran-4-yl)-N-hydroxyformamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Gentamicin Molecular Formula: C21H41N5O9
Molecular Weight: 507.6
Storage: Store in a cool, dry place.