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VAQORACHEMICALS
Impurity reference standards

Ibrutinib impurities & reference standards

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

88reference materials
2nitrosamine impurities
2isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Ibrutinib WS
936563-96-1 · C25H24N6O2
View API
Reference Standard
(S)-Ibrutinib chemical structure
(S)-Ibrutinib
CAS
936563-97-2
Formula
C25H24N6O2
MW
440.5 g/mol
In stock
Reference Standard
4-Hydroxy Ibrutinib chemical structure
4-Hydroxy Ibrutinib
CAS
1288339-18-3
Formula
C25H24N6O3
MW
456.5 g/mol
VQ-048600
Reference Standard
Fenebrutinib chemical structure
Fenebrutinib
CAS
1434048-34-6
Formula
C37H44N8O4
MW
664.8 g/mol
VQ-037614
Reference Standard
Ibrutinib Impurity 13
Ibrutinib Impurity 13
CAS
167112-94-9
Formula
C10H10ClNO5.C5H11NO
MW
360.79 g/mol
VQ-048604

FAQs — Ibrutinib impurities

Which Ibrutinib impurities do you supply?

We list 88 Ibrutinib-related reference materials, including process impurities, degradation products, nitrosamine impurities, stable-isotope-labelled standards and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.

What are Ibrutinib 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 Ibrutinib 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 Ibrutinib impurity standards

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