1-((2-Fluorophenyl)carbamoyl)cyclopropane-1-carboxylic Acid
- CAS
- 918642-61-2
- Formula
- C11H10FNO3
- MW
- 223.2 g/mol
VQ-024722
Impurity reference standards
Cabozantinib impurities & reference standards
Characterised Cabozantinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
40reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Cabozantinib WS
849217-68-1 · C28H24FN3O5
1-((3-Fluorophenyl)carbamoyl)cyclopropane-1-carboxylic Acid
- CAS
- 1247859-37-5
- Formula
- C11H10FNO3
- MW
- 223.2 g/mol
VQ-035349
1-(Phenylcarbamoyl)cyclopropane-1-carboxylic Acid
- CAS
- 145591-80-6
- Formula
- C11H11NO3
- MW
- 205.21 g/mol
VQ-044567
5-(((3,4-Dimethoxyphenyl)amino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione
- CAS
- 213699-53-7
- Formula
- C15H17NO6
- MW
- 307.3 g/mol
VQ-042575
Cabozantinib Des Cyclopropanyl Acetamide Impurity
- CAS
- 651054-52-3
- Formula
- C19H18N2O4
- MW
- 338.4 g/mol
VQ-029576
Methyl 1-((4-fluorophenyl)carbamoyl)cyclopropane-1-carboxylate
- CAS
- 1345847-71-3
- Formula
- C12H12FNO3
- MW
- 237.23 g/mol
VQ-024719
N-(4-((6,7-Dimethoxyquinolin-4-yl)oxy)phenyl)-N-(4-fluoro-2-hydroxyphenyl)cyclopropane-1,1-dicarboxamide
- CAS
- 1628530-38-0
- Formula
- C28H24FN3O6
- MW
- 517.5 g/mol
VQ-029579
N-(4-((6,7-Dimethoxyquinolin-4-yl)oxy)phenyl)-N-(4-fluorophenyl)-N-methylcyclopropane-1,1-dicarboxamide
- CAS
- 2458244-61-4
- Formula
- C29H26FN3O5
- MW
- 515.54 g/mol
VQ-044934
N-(4-Fluorophenyl)-N-(4-((7-hydroxy-6-methoxyquinolin-4-yl)oxy)phenyl)cyclopropane-1,1-dicarboxamide
- CAS
- 1628530-42-6
- Formula
- C27H22FN3O5
- MW
- 487.5 g/mol
VQ-020691
N,N'-Bis(4-((6,7-dimethoxyquinolin-4-yl)oxy)phenyl)cyclopropane-1,1-dicarboxamide
- CAS
- 2439164-91-5
- Formula
- C39H34N4O8
- MW
- 686.7 g/mol
VQ-024721
N,N'-Bis(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
- CAS
- 1431468-36-8
- Formula
- C17H14F2N2O2
- MW
- 316.3 g/mol
VQ-024723
FAQs — Cabozantinib impurities
Which Cabozantinib impurities do you supply?
We list 40 Cabozantinib-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 Cabozantinib 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 Cabozantinib 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 Cabozantinib impurity standards
We reply within one business day with price, pack options, lead time and documentation.