This impurity is related to Tacrolimus Hydroxy Acid 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 Hydroxy Acid 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,25aS,E)-8-Allyl-5,15,19-trihydroxy-3-((E)-1-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl)-14,16-dimethoxy-4,10,12,18-tetramethyl-1,7,20-trioxo-1,3,4,5,6,7,8,11,12,13,14,15,16,17,18,19,20,22,23,24,25,25a-docosahydropyrido[2,1-c][1]oxa[4]azacyclodocosine-19-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C44H71NO13
Molecular Weight: 822
Storage: Store in a cool, dry place.