Impurity reference standards
Binimetinib impurities & reference standards
Characterised Binimetinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
28reference materials
4nitrosamine impurities
COAHPLC · NMR · MS on request
Parent API: Binimetinib WS
606143-89-9 · C17H15BrF2N4O3
![5-((4-Bromo-2-fluorophenyl)amino)-4-fluoro-1-methyl-N-(2-(vinyloxy)ethoxy)-1H-benzo[d]imidazole-6-carboxamide chemical structure](/media/structures/KMJNEXZZHQIVEF-UHFFFAOYSA-N.svg)
5-((4-Bromo-2-fluorophenyl)amino)-4-fluoro-1-methyl-N-(2-(vinyloxy)ethoxy)-1H-benzo[d]imidazole-6-carboxamide
- CAS
- 1415559-75-9
- Formula
- C19H17BrF2N4O3
- MW
- 467.3 g/mol
VQ-032850
![Methyl 4-fluoro-5-((2-fluorophenyl)amino)-1-methyl-1H-benzo[d]imidazole-6-carboxylate chemical structure](/media/structures/NYPSEISJJRRIAX-UHFFFAOYSA-N.svg)
Methyl 4-fluoro-5-((2-fluorophenyl)amino)-1-methyl-1H-benzo[d]imidazole-6-carboxylate
- CAS
- 1415559-89-5
- Formula
- C16H13F2N3O2
- MW
- 317.29 g/mol
VQ-029447
FAQs — Binimetinib impurities
Which Binimetinib impurities do you supply?
We list 28 Binimetinib-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 Binimetinib 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 Binimetinib 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 Binimetinib impurity standards
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