Letermovir Di N-Oxide Impurity

Name: Letermovir Di N-Oxide Impurity
Brand: Vaqora Chemicals
SKU: VQ-007187

About Letermovir Di N-Oxide Impurity

Letermovir Di N-Oxide Impurity is a metabolite or degradation product of Letermovir from the Vaqora Chemicals catalogue, specified at 95.86% purity. The compound has the formula C29H28F4N4O6, corresponding to a molecular weight of 604.55 g/mol.

The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Good laboratory practice and suitable PPE are recommended during handling.

Analytical teams use this compound to identify metabolites and degradants of Letermovir, to validate stability-indicating methods (AMV) and to support QC and regulatory filings. It is used across pharmaceutical manufacturing and academic and industrial research.

We offer Letermovir Di N-Oxide Impurity in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers worldwide. Stock is available for quick dispatch.

Typical applications

Metabolite identification
Stability-indicating methods
Impurity profiling

Industries

Related to Letermovir

View every impurity, metabolite and intermediate we list for Letermovir.

Letermovir impurities

Specifications & identifiers

Chemical identifiers
Product name	Letermovir Di N-Oxide Impurity
Catalogue No.	VQ-007187
Molecular formula	C₂₉H₂₈F₄N₄O₆
Molecular weight	604.55 g/mol
Grade	Reference Standard
Purity / assay	95.86%
HSN code	38229090

Physical properties
Physical form	Solid

Documents

Safety Data Sheet (SDS)16-section GHS · on request Certificate of AnalysisTypical / batch COA · on request Specification sheetTDS / MOA · on request

Frequently asked questions

What is the molecular formula and molecular weight of Letermovir Di N-Oxide Impurity?

Letermovir Di N-Oxide Impurity has the molecular formula C29H28F4N4O6 and a molecular weight of 604.55 g/mol.

What is Letermovir Di N-Oxide Impurity used for?

Letermovir Di N-Oxide Impurity is supplied as a characterised reference material related to Letermovir. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.

Which grade and pack sizes of Letermovir Di N-Oxide Impurity can I order?

We supply Letermovir Di N-Oxide Impurity in Reference Standard (95.86%) grade, in 10 mg, 25 mg, 50 mg, 100 mg, 250 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Letermovir Di N-Oxide Impurity?

Yes. Every lot of Letermovir Di N-Oxide Impurity is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.

Can Letermovir Di N-Oxide Impurity be shipped internationally?

Yes. We export Letermovir Di N-Oxide Impurity worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.