Ezetimibe Stage-ll Impurity | CAS 272778-12-8 - Request Quote
Ezetimibe Stage-ll Impurity
| SZ CAT No: | SZ-E026073 |
| CAS No | 272778-12-8 |
| Mol.F. | C39H46F2N2O5Si2 |
| Mol.Wt. | 717.0 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Ezetimibe Stage-ll Impurity is chemically (S)-3-((2R,5S)-5-(4-Fluorophenyl)-2-((S)-((4-fluorophenyl)amino)(4-((trimethylsilyl)oxy)phenyl)methyl)-5-((trimethylsilyl)oxy)pentanoyl)-4-phenyloxazolidin-2-one. Ezetimibe Stage-ll Impurity is supplied with detailed characterization data compliant with regulatory guideline. Ezetimibe Stage-ll 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 Ezetimibe.
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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Ezetimibe Stage-ll Impurity for Method Validation
Ezetimibe Reference Standard
Ezetimibe Stage-ll Impurity for ANDA Filing
Ezetimibe Stage-ll Impurity for Forced Degradation Studies
Ezetimibe Stage-ll Impurity Identification Standards
Ezetimibe Stage-ll Impurity for DMF Filing
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