Tacrolimus Impurity 17 - Request Quote
Tacrolimus Impurity 17
| SZ CAT No: | SZ-T005063 |
| CAS No | NA |
| Mol.F. | C46H75NO13 |
| Mol.Wt. | 850.1 |
| Inv. Status | Under Synthesis |
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Tacrolimus Impurity 17 is chemically Ethyl (3S,4R,12S,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-carboxylate. Tacrolimus Impurity 17 is supplied with detailed characterization data compliant with regulatory guideline. Tacrolimus Impurity 17 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Tacrolimus.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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