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VAQORACHEMICALS
Impurity reference standards

Axitinib impurities & reference standards

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

29reference materials
2isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Axitinib WS
319460-85-0 · C22H18N4OS
View API
Reference Standard
6-Nitroindazole chemical structure
6-Nitroindazole
CAS
7597-18-4
Formula
C7H5N3O2
MW
163.13 g/mol
VQ-032923
Reference Standard
Axitinib Acid chemical structure
Axitinib Acid
CAS
319462-34-5
Formula
C21H15N3O2S
MW
373.4 g/mol
VQ-029311
Reference Standard
Axitinib Amide chemical structure
Axitinib Amide
CAS
319462-41-4
Formula
C21H16N4OS
MW
372.4 g/mol
VQ-043062
Reference Standard
Axitinib Impurity H chemical structure
Axitinib Impurity H
CAS
1639137-80-6
Formula
C24H20N4O2S
MW
428.5 g/mol
VQ-024460
Reference Standard
Axitinib Sulfoxide chemical structure
Axitinib Sulfoxide
CAS
1347304-18-0
Formula
C22H18N4O2S
MW
402.5 g/mol
VQ-021687
Reference Standard
Axitinib WS chemical structure
Axitinib WS
CAS
319460-85-0
Formula
C22H18N4OS
MW
386.5 g/mol
In stock
Reference Standard
Axitinib Z-isomer chemical structure
Axitinib Z-isomer
CAS
885126-40-9
Formula
C22H18N4OS
MW
386.5 g/mol
VQ-024454
Reference Standard
Axitinib-13C d3 chemical structure
Axitinib-13C d3
CAS
1261432-00-1
Formula
C22H18N4OS
MW
390.5 g/mol
VQ-043380
Reference Standard
Axitinib-d3 chemical structure
Axitinib-d3
CAS
1126623-89-9
Formula
C22H18N4OS
MW
389.5 g/mol
VQ-043379

FAQs — Axitinib impurities

Which Axitinib impurities do you supply?

We list 29 Axitinib-related reference materials, including process impurities, degradation products, 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 Axitinib 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 Axitinib 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 Axitinib impurity standards

We reply within one business day with price, pack options, lead time and documentation.

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