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VAQORACHEMICALS
Impurity reference standards

Tivozanib impurities & reference standards

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

18reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Tivozanib
475108-18-0 · C22H19ClN4O5
View API
Reference Standard
Tivozanib chemical structure
Tivozanib
CAS
475108-18-0
Formula
C22H19ClN4O5
MW
454.9 g/mol
VQ-007802
Reference Standard
Tivozanib Impurity B
Tivozanib Impurity B
CAS
3051498-34-8
Formula
C24H19ClN2O5
MW
450.87 g/mol
In stock
Reference Standard
Tivozanib Impurity C chemical structure
Tivozanib Impurity C
CAS
3051498-20-2
Formula
C35H28Cl2N4O7
MW
687.5 g/mol
In stock

FAQs — Tivozanib impurities

Which Tivozanib impurities do you supply?

We list 18 Tivozanib-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 Tivozanib 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 Tivozanib 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 Tivozanib impurity standards

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