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Impurity reference standards

Letermovir impurity standards

For Letermovir, the Zemixal catalogue holds 12 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Most entries are process-related impurities, synthesis intermediates and isomers.

12reference materials
Letermovir structure
Parent API

Letermovir

CAS
917389-32-3
Formula
C29H28F4N4O4
MW
572.5 g/mol
Code
ZX-006608

Every standard comes with a certificate of analysis. Structure confirmation data, typically NMR, MS and chromatographic purity, is available on request. They are bought for system suitability, peak identification, quantitation against limits and the impurity justification sections of regulatory submissions.

All Letermovir reference materials

1–12 of 12 standards
Methyl
CAS
917389-21-0
Formula
C19H16F4N2O4
MW
412.3 g/mol
ZX-047872
Questions

Letermovir impurities, answered

What Letermovir reference materials are available?
The catalogue currently lists 12 compounds for Letermovir. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Letermovir impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Letermovir impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.

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