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Ezetimibe Impurity 50 - Request Quote

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Ezetimibe Impurity 50

SZ CAT No:SZ-E026117
CAS No
NA
Mol.F.
C39H46F2N2O5Si2
Mol.Wt.
717.0
Inv. Status
Synthesis on demand

Chemical Name :

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Usage Note:

Ezetimibe Impurity 50 is chemically (S)-3-((2S,5S)-5-(4-fluorophenyl)-2-((S)-((4-fluorophenyl)amino)(4-((trimethylsilyl)oxy)phenyl)methyl)-5-((trimethylsilyl)oxy)pentanoyl)-4-phenyloxazolidin-2-one. Ezetimibe Impurity 50 is supplied with detailed characterization data compliant with regulatory guideline. Ezetimibe Impurity 50 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 Impurity 50 for Method Validation

Ezetimibe Reference Standard

Ezetimibe Impurity 50 for ANDA Filing

Ezetimibe Impurity 50 for Forced Degradation Studies

Ezetimibe Impurity 50 Identification Standards

Ezetimibe Impurity 50 for DMF Filing

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SynZeal will update these details as per new developments or findings in product specifications without further notice.

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