This impurity is related to Selamectin EP Impuity 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.
Selamectin EP Impuity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2aE,2'R,4E,4'S,5'S,6S,6'R,7S,8E,11R,15S,17aR,20Z,20aR,20bS)-6'-Cyclohexyl-7-[(2,6-dideoxy-3-O-methyl-a-L-arabino-hexopyranosyl)oxy]-4',20b-dihydroxy-20-(hydroxyimino)-5',6,8,19-tetramethyl-3',4',5',6,6',7,10,11,14,15,17a,20,20a,20b-tetradecahydrospiro[2H,17H-11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-17-one ((5Z,21R,23S,25R)-25-cyclohexyl-4'-O-de(2,6-dideoxy-3-O-methyl-a-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-23-hydroxy-5-(hydroxyimino)avermectin A1a)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Selamectin Molecular Formula: C43H63NO12
Molecular Weight: 786
Storage: Store in a cool, dry place.