This impurity is related to Tacrolimus Ring-Opening Impurity 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.
Tacrolimus Ring-Opening Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3S,4R,5S,8R,12S,14S,15R,16S,18R,26aS,Z)-8-Allyl-5,15-dihydroxy-3-((E)-1-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl)-14,16-dimethoxy-4,10,12,18-tetramethyl-5,6,11,12,13,14,15,16,17,18,24,25,26,26a-tetradecahydro-3H-pyrido[2,1-c][1]oxa[4]azacyclotricosine-1,7,19,20,21(4H,8H,23H)-pentaoneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C44H69NO12
Molecular Weight: 804
Storage: Store in a cool, dry place.