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VAQORACHEMICALS
Impurity reference standards

Nilotinib impurities & reference standards

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

72reference materials
1nitrosamine impurities
3isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Nilotinib
641571-10-0 · C28H22F3N7O
View API
Reference Standard
N-Nitroso Nilotinib chemical structure
N-Nitroso Nilotinib
CAS
2925306-68-7
Formula
C28H21F3N8O2
MW
558.5 g/mol
VQ-026911
Reference Standard
Nilotinib chemical structure
Nilotinib
CAS
641571-10-0
Formula
C28H22F3N7O
MW
529.5 g/mol
In stock
Reference Standard
Nilotinib CRS
Nilotinib CRS
Formula
C28H22F3N7O.ClH.C27H20F3N7O.C29H24F3N7O.C18H16N4O2
MW
2265.71 g/mol
In stock

FAQs — Nilotinib impurities

Which Nilotinib impurities do you supply?

We list 72 Nilotinib-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 Nilotinib 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 Nilotinib 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 Nilotinib impurity standards

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