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Impurity reference standards

Deucravacitinib impurity standards

For Deucravacitinib, the Zemixal catalogue holds 10 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 2 metabolites or hydroxylated analogues.

10reference materials
2metabolites
Deucravacitinib structure
Parent API

Deucravacitinib

CAS
1609392-27-9
Formula
C20H22N8O3
MW
425.5 g/mol
Code
ZX-006492

Batches are supplied with a certificate of analysis, and the supporting spectra can be sent ahead of a purchase order so your QA team can review them. Typical uses are method development and validation, relative response factor work, forced degradation studies and the impurity sections of ANDA, DMF or CEP filings.

By impurity type

Metabolites2Hydroxy, desmethyl and conjugated forms

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

All Deucravacitinib reference materials

1–10 of 10 standards
Questions

Deucravacitinib impurities, answered

What Deucravacitinib reference materials are available?
The catalogue currently lists 10 compounds for Deucravacitinib, including 2 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 Deucravacitinib 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 Deucravacitinib 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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