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VAQORACHEMICALS
Impurity reference standards

Ruxolitinib impurities & reference standards

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

51reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Ruxolitinib WS
941678-49-5 · C17H18N6
View API
Reference Standard
rac-Ruxolitinib chemical structure
rac-Ruxolitinib
CAS
941688-05-7
Formula
C17H18N6
MW
306.4 g/mol
In stock
Reference Standard
rac-Ruxolitinib-d9 chemical structure
rac-Ruxolitinib-d9
CAS
2469553-67-9
Formula
C17H18N6
MW
315.42 g/mol
VQ-042051
Reference Standard
Ruxolitinib (sm)
Ruxolitinib (sm)
Formula
C12H18BrN3OSi
MW
328.28 g/mol
In stock
Reference Standard
Ruxolitinib Amide chemical structure
Ruxolitinib Amide
CAS
1911644-32-0
Formula
C17H20N6O
MW
324.4 g/mol
In stock
Reference Standard
Ruxolitinib d8 chemical structure
Ruxolitinib d8
CAS
1513883-39-0
Formula
C17H18N6
MW
314.41 g/mol
VQ-045063
Reference Standard
Ruxolitinib M18 chemical structure
Ruxolitinib M18
CAS
1315607-85-2
Formula
C17H18N6O
MW
322.4 g/mol
VQ-033715
Reference Standard
Ruxolitinib M27 chemical structure
Ruxolitinib M27
CAS
1809535-63-4
Formula
C17H18N6O
MW
322.4 g/mol
VQ-033714
Reference Standard
Ruxolitinib WS chemical structure
Ruxolitinib WS
CAS
941678-49-5
Formula
C17H18N6
MW
306.4 g/mol
In stock
Reference Standard
RXP-2 PDMA
RXP-2 PDMA
Formula
C19H25N7O
MW
367.45 g/mol
In stock
Reference Standard
RXP-3 PDMA chemical structure
RXP-3 PDMA
Formula
C19H23N7
MW
349.4 g/mol
In stock
Reference Standard
S-Ruxolitinib chemical structure
S-Ruxolitinib
CAS
941685-37-6
Formula
C17H18N6
MW
306.4 g/mol
In stock

FAQs — Ruxolitinib impurities

Which Ruxolitinib impurities do you supply?

We list 51 Ruxolitinib-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 Ruxolitinib 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 Ruxolitinib 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 Ruxolitinib impurity standards

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