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Impurity reference standards

Tivozanib impurity standards

16 characterised compounds linked to Tivozanib are catalogued here, from named pharmacopoeial impurities to synthesis intermediates and breakdown products. Highlights of the range are 2 metabolites or hydroxylated analogues.

16reference materials
2metabolites
Tivozanib structure
Parent API

Tivozanib

CAS
475108-18-0
Formula
C22H19ClN4O5
MW
454.9 g/mol
Code
ZX-006865

Batches are supplied with a certificate of analysis, and the supporting spectra can be sent ahead of a purchase order so your QA team can review them. Laboratories use them to validate related-substance methods, set specification limits under ICH Q3A and Q3B, and identify unknown peaks in stability samples.

By impurity type

Metabolites2Hydroxy, desmethyl and conjugated forms

Counts are based on product names. One compound can fall into more than one type.

All Tivozanib reference materials

1–16 of 16 standards
Questions

Tivozanib impurities, answered

How many Tivozanib impurity standards does Zemixal list?
The catalogue currently lists 16 compounds for Tivozanib, including 2 metabolites or hydroxylated analogues. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Tivozanib impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Tivozanib impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.
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