This impurity is related to Vincristine Sulfate EP Impurity A 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.
Vincristine Sulfate EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Methyl (3aR,4R,5S,5aR,10bR,13aR)-4-(acetyloxy)-3a-ethyl-9-[(5R,7S,9S)-5-ethyl-5,6-dihydroxy-9-(methoxycarbonyl)-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl]-6-formyl-5-hydroxy-8-methoxy-3a,4,5,5a,6,11,12,13a-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Vincristine Sulfate Molecular Formula: C46H56N4O11
Molecular Weight: 841
Storage: Store in a cool, dry place.