This impurity is related to Tacrolimus EP Impurity F 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 EP Impurity F 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)-5,15-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,5,6,11,12,13,14,15,16,17,18,24,25,26,26a- hexadecahydro-7H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,19,20,21(8H,23H)-pentone Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C43H67NO12
Molecular Weight: 790
Storage: Store in a cool, dry place.