Lusutrombopag Hydroxy Impurity - Request Quote
Lusutrombopag Hydroxy Impurity
| SZ CAT No: | SZ-L055005 |
| CAS No | NA |
| Mol.F. | C29H32Cl2N2O6S |
| Mol.Wt. | 607.5 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Lusutrombopag Hydroxy Impurity is chemically (S,E)-3-(2,6-Dichloro-4-((4-(3-(1-((6-hydroxyhexyl)oxy)ethyl)-2-methoxyphenyl)thiazol-2-yl)carbamoyl)phenyl)-2-methylacrylic acid. Lusutrombopag Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Lusutrombopag Hydroxy 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 Lusutrombopag.
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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Lusutrombopag Hydroxy Impurity for Method Validation
Lusutrombopag Reference Standard
Lusutrombopag Hydroxy Impurity for ANDA Filing
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Lusutrombopag Hydroxy Impurity Identification Standards
Lusutrombopag Hydroxy Impurity for DMF Filing
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