This impurity is related to Tacrolimus Dehydro 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 Dehydro Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:15,?19-?Epoxy-?3H-?pyrido[2,?1-?c]?[1,?4]?oxaazacyclotricosine?-?1,?7,?20,?21(4H,?23H)?-?tetrone, 8,?11,?12,?13,?14,?15,?16,?17,?18,?19,?24,?25,?26,?26a-?tetradecahydro-?19-?hydroxy-?3-?[2-?(4-?hydroxy-?3-?methoxycyclohexyl)?-?1-?methylethenyl]?-?14,?16-?dimethoxy-?4,?10,?12,?18-?tetramethyl-?8-?(2-?propenyl)?-?, [3S-?[3R*[E(1S*,?3S*,?4S*)?]?,?4S*,?5E,?8R*,?9E,?12R*,?14R*,?15S*,?16R*,?18S*,?26aR*]?]?- (9CI)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C44H67NO11
Molecular Weight: 786
Storage: Store in a cool, dry place.