Impurity reference standards
Lenvatinib impurities & reference standards
Characterised Lenvatinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
56reference materials
COAHPLC · NMR · MS on request
Parent API: Lenvatinib
417716-92-8 · C21H19ClN4O4
4-(4-(3-Cyclopropylureido)phenoxy)-7-methoxyquinoline-6-carboxamide
- CAS
- 417714-14-8
- Formula
- C21H20N4O4
- MW
- 392.4 g/mol
VQ-048831
4-(4-Amino-3-chlorophenoxy)-7-methoxyquinoline-6-carbonitrile
- CAS
- 2023826-16-4
- Formula
- C17H12ClN3O2
- MW
- 325.7 g/mol
VQ-031484
4-(4-Amino-3-chlorophenoxy)-7-methoxyquinoline-6-carboxylic Acid
- CAS
- 2712290-12-3
- Formula
- C17H13ClN2O4
- MW
- 344.7 g/mol
VQ-037946
![4-[(Z)-(2-Chloro-4-hydroxyphenyl)diazenyl]benzene-1-sulfonic acid chemical structure](/media/structures/GQRUMXSXCFMAQE-UHFFFAOYSA-N.svg)
4-[(Z)-(2-Chloro-4-hydroxyphenyl)diazenyl]benzene-1-sulfonic acid
- CAS
- 253801-34-2
- Formula
- C12H9ClN2O4S
- MW
- 312.73 g/mol
VQ-034297
5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione
- CAS
- 15568-85-1
- Formula
- C8H10O5
- MW
- 186.16 g/mol
VQ-042574
7-Methoxy-4-oxo-1,4-dihydroquinoline-6-carbonitrile
- CAS
- 417721-15-4
- Formula
- C11H8N2O2
- MW
- 200.19 g/mol
VQ-048832
7-Methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylic acid
- CAS
- 417721-34-7
- Formula
- C11H9NO4
- MW
- 219.19 g/mol
VQ-044000
Lenvatinib N-Ethyl Impurity methanesulfonate salt
- CAS
- 2991278-65-8
- Formula
- C20H19ClN4O4 : CH4O3S
- MW
- 510.95 g/mol
VQ-048835
Methyl 4-(((2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)methyl)amino)-2-methoxybenzoate
- CAS
- 205448-64-2
- Formula
- C16H17NO7
- MW
- 335.31 g/mol
VQ-031487
Methyl 4-chloro-7-methoxyquinoline-6-carboxylate
- CAS
- 205448-66-4
- Formula
- C12H10ClNO3
- MW
- 251.66 g/mol
In stock
Methyl 7-methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylate
- CAS
- 205448-65-3
- Formula
- C12H11NO4
- MW
- 233.22 g/mol
VQ-023394
FAQs — Lenvatinib impurities
Which Lenvatinib impurities do you supply?
We list 56 Lenvatinib-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Lenvatinib 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 Lenvatinib 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 Lenvatinib impurity standards
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