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Impurity reference standards

Ruxolitinib impurity standards

For Ruxolitinib, the Zemixal catalogue holds 38 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 3 metabolites or hydroxylated analogues.

38reference materials
3metabolites
Ruxolitinib WS structure
Parent API

Ruxolitinib WS

CAS
941678-49-5
Formula
C17H18N6
MW
306.4 g/mol
Code
ZX-006800

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.

By impurity type

Metabolites3Hydroxy, desmethyl and conjugated forms

Counts are based on product names. One compound can fall into more than one type.

All Ruxolitinib reference materials

1–38 of 38 standards
Questions

Ruxolitinib impurities, answered

What Ruxolitinib reference materials are available?
The catalogue currently lists 38 compounds for Ruxolitinib, including 3 metabolites or hydroxylated analogues. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Ruxolitinib 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 Ruxolitinib 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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