This impurity is related to N-Nitroso Candesartan Impurity 12 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.
N-Nitroso Candesartan Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:1-(((cyclohexyloxy)carbonyl)oxy)ethyl 2-ethoxy-1-nitroso-1H-benzo[d]imidazole-7-carboxylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Candesartan Molecular Formula: C32H33N7O7
Molecular Weight: 627.65
Storage: Store in a cool, dry place.