This impurity is related to Desmethyl Tacrolimus 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.
Desmethyl Tacrolimus is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-8-Allyl-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[(E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylvinyl]-14,16-dimethoxy-4,12,18-trimethyl-15,19-epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21-(4H,23H)-tetrone (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C43H67NO12
Molecular Weight: 790
Storage: Store in a cool, dry place.