Impurity reference standards
Zanubrutinib impurities & reference standards
Characterised Zanubrutinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
10reference materials
COAHPLC · NMR · MS on request
![(S)-2-(4-Phenoxyphenyl)-7-(piperidin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide chemical structure](/media/structures/GNEOXABCHHVVEA-FQEVSTJZSA-N.svg)
(S)-2-(4-Phenoxyphenyl)-7-(piperidin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide
- CAS
- 1633352-71-2
- Formula
- C24H27N5O2
- MW
- 417.5 g/mol
VQ-035499
![(S)-7-(1-(3-Chloropropanoyl)piperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide chemical structure](/media/structures/YAVZMBVVGZCZAE-QFIPXVFZSA-N.svg)
(S)-7-(1-(3-Chloropropanoyl)piperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide
- CAS
- 1633351-79-7
- Formula
- C27H30ClN5O3
- MW
- 508 g/mol
VQ-044554
![(S)-7-(1-Acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile chemical structure](/media/structures/QMQFPTAEMQLQKQ-DEOSSOPVSA-N.svg)
(S)-7-(1-Acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile
- CAS
- 2432022-47-2
- Formula
- C27H27N5O2
- MW
- 453.5 g/mol
VQ-035341
3-Amino-5-(4-phenoxyphenyl)pyrazole-4-carbonitrile
- CAS
- 330792-70-6
- Formula
- C16H12N4O
- MW
- 276.29 g/mol
VQ-039962
![tert-Butyl 4-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)piperidine-1-carboxylate chemical structure](/media/structures/KMWRWUBEVNQXEE-UHFFFAOYSA-N.svg)
tert-Butyl 4-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)piperidine-1-carboxylate
- CAS
- 2190506-55-7
- Formula
- C29H29N5O3
- MW
- 495.6 g/mol
VQ-042993
FAQs — Zanubrutinib impurities
Which Zanubrutinib impurities do you supply?
We list 10 Zanubrutinib-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 Zanubrutinib 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 Zanubrutinib 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 Zanubrutinib impurity standards
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