This impurity is related to Tacrolimus Impurity 1 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 Impurity 1 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:[3S-[3R*[E(1S*,3S*,4S*)],4S*,5R*,8S*,9E,12R*,14R*,15S*,16R*,18S*,19S*,25aR*]]-3,4,5,6,8,11,12,13,14,15,16,17,18,19,23,24,25a-Octadecahydro-5,19-dihydroxy-3-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propenyl)-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclodocosine-1,7,20(22H)-trionCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tacrolimus Molecular Formula: C43H69NO11
Molecular Weight: 776
Storage: Store in a cool, dry place.