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VAQORACHEMICALS
Impurity reference standards

Deucravacitinib impurities & reference standards

Characterised Deucravacitinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.

28reference materials
COAHPLC · NMR · MS on request
Parent API: Deucravacitinib
1609392-27-9 · C20H22N8O3
View API
Reference Standard
Deucravacitinib chemical structure
Deucravacitinib
CAS
1609392-27-9
Formula
C20H22N8O3
MW
425.5 g/mol
In stock
Reference Standard
Deucravacitinib D3
Deucravacitinib D3
CAS
2704587-20-0
Formula
C20H16D6N8O3
MW
428.49 g/mol
VQ-047999

FAQs — Deucravacitinib impurities

Which Deucravacitinib impurities do you supply?

We list 28 Deucravacitinib-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.

What are Deucravacitinib impurity standards used for?

They are used for analytical method development and validation, impurity identification and quantification, forced-degradation and stability studies, and to support ANDA, DMF and other regulatory submissions under ICH Q3A/Q3B (and ICH M7 for mutagenic impurities).

Can you synthesise a Deucravacitinib impurity that is not listed?

Yes. Our custom synthesis service can prepare and characterise unlisted impurities, metabolites and labelled analogues from milligram to gram scale. Share the structure or name and required quantity for a quotation.

Request Deucravacitinib impurity standards

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