This impurity is related to Imidacloprid 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.
Imidacloprid EP impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N-(1-((6-((2-(((6-Chloropyridin-3-yl)methyl)amino)ethyl)amino)pyridin-3-yl)methyl)-4,5-dihydro-1H-imidazol-2-yl)nitramideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Imidacloprid Molecular Formula: C17H21ClN8O2
Molecular Weight: 404.9
Storage: Store in a cool, dry place.