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Letermovir N-Oxide Impurity 2 - Request Quote

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Letermovir N-Oxide Impurity 2

SZ CAT No:SZ-L052041
CAS No
NA
Mol.F.
C29H28F4N4O5
Mol.Wt.
588.6
Inv. Status
Synthesis on demand

Chemical Name :

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Usage Note:

Letermovir N-Oxide Impurity 2 is chemically (S)-1-(4-(carboxymethyl)-8-fluoro-3-(2-methoxy-5-(trifluoromethyl)phenyl)-3,4-dihydroquinazolin-2-yl)-4-(3-methoxyphenyl)piperazine 1-oxide. Letermovir N-Oxide Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Letermovir N-Oxide Impurity 2 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 Letermovir.

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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Letermovir N-Oxide Impurity 2 for Method Validation

Letermovir Reference Standard

Letermovir N-Oxide Impurity 2 for ANDA Filing

Letermovir N-Oxide Impurity 2 for Forced Degradation Studies

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Letermovir N-Oxide Impurity 2 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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