This impurity is related to Levosimendan 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.
Levosimendan Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(5R,5'R)-6,6'-(((Z)-Triaz-1-ene-1,3-diyl)bis(4,1-phenylene))bis(5-methyl-4,5-dihydropyridazin-3(2H)-one)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: levosimendan Molecular Formula: C22H23N7O2
Molecular Weight: 417.5
Storage: Store in a cool, dry place.