Letermovir Impurity LTRRC-8

Name: Letermovir Impurity LTRRC-8
Brand: Vaqora Chemicals
SKU: VQ-005174

About Letermovir Impurity LTRRC-8

Letermovir Impurity LTRRC-8 is an impurity of Letermovir from the Vaqora Chemicals catalogue at a purity of 96%. Formula C30H30F4N4O4.C20H18O8.C4H8O2, molecular weight 1061.03 g/mol. It is also known as Ethyl acetate.

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.

This Letermovir impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. It is used across pharmaceutical manufacturing and academic and industrial research.

We offer Letermovir Impurity LTRRC-8 in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers worldwide. This item is currently in stock for prompt dispatch.

Typical applications

Analytical method development
Method validation (AMV)
QC release testing
ANDA / DMF filings

Industries

Related to Letermovir

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

Letermovir impurities

Specifications & identifiers

Chemical identifiers
Product name	Letermovir Impurity LTRRC-8
Catalogue No.	VQ-005174
Molecular formula	C₃₀H₃₀F₄N₄O₄.C₂₀H₁₈O₈.C₄H₈O₂
Molecular weight	1061.03 g/mol
Grade	Reference Standard
Purity / assay	96%
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 Impurity LTRRC-8?

Letermovir Impurity LTRRC-8 has the molecular formula C30H30F4N4O4.C20H18O8.C4H8O2 and a molecular weight of 1061.03 g/mol.

What is Letermovir Impurity LTRRC-8 used for?

Letermovir Impurity LTRRC-8 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 Impurity LTRRC-8 can I order?

We supply Letermovir Impurity LTRRC-8 in Reference Standard (96%) grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Letermovir Impurity LTRRC-8?

Yes. Every lot of Letermovir Impurity LTRRC-8 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 Impurity LTRRC-8 be shipped internationally?

Yes. We export Letermovir Impurity LTRRC-8 worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.