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Impurity reference standards

Firocoxib impurity standards

This page brings together 11 Firocoxib related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. The range includes 2 metabolites or hydroxylated analogues and 1 degradation product.

11reference materials
2metabolites
1degradants
Firocoxib structure
Parent API

Firocoxib

CAS
189954-96-9
Formula
C17H20O5S
MW
336.4 g/mol
Code
ZX-006555

Every standard comes with a certificate of analysis. Structure confirmation data, typically NMR, MS and chromatographic purity, is available on request. 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
Degradants1N-oxides, dimers, lactones and breakdown products

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

All Firocoxib reference materials

1–11 of 11 standards
Questions

Firocoxib impurities, answered

What Firocoxib reference materials are available?
The catalogue currently lists 11 compounds for Firocoxib, including 2 metabolites or hydroxylated analogues and 1 degradation product. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Firocoxib 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 Firocoxib 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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