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VAQORACHEMICALS
Impurity reference standards

Selumetinib impurities & reference standards

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

9reference materials
2nitrosamine impurities
COAHPLC · NMR · MS on request
Parent API: Selumetinib
606143-52-6 · C17H15BrClFN4O3
View API
Reference Standard
Selumetinib chemical structure
Selumetinib
CAS
606143-52-6
Formula
C17H15BrClFN4O3
MW
457.7 g/mol
VQ-007748

FAQs — Selumetinib impurities

Which Selumetinib impurities do you supply?

We list 9 Selumetinib-related reference materials, including process impurities, degradation products, nitrosamine impurities and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.

What are Selumetinib 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 Selumetinib 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 Selumetinib impurity standards

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