Tacrolimus Dehydro Impurity | CAS 129212-37-9 - Request Quote
Tacrolimus Dehydro Impurity
| SZ CAT No: | SZ-T005013 |
| CAS No | 129212-37-9 |
| Mol.F. | C44H67NO11 |
| Mol.Wt. | 786.0 |
| Inv. Status | In Stock |
| Shipping Condition | Ice Pack shipment |
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Tacrolimus Dehydro Impurity is chemically 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). Tacrolimus Dehydro Impurity is supplied with detailed characterization data compliant with regulatory guideline. Tacrolimus Dehydro Impurity 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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Tacrolimus Dehydro Impurity for Method Validation
Tacrolimus Reference Standard
Tacrolimus Dehydro Impurity for ANDA Filing
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Tacrolimus Dehydro Impurity Identification Standards
Tacrolimus Dehydro Impurity for DMF Filing
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