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Impurity reference standards

Celecoxib impurity standards

Zemixal lists 30 reference materials related to Celecoxib, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 3 pharmacopoeial impurities and 4 metabolites or hydroxylated analogues.

30reference materials
3pharmacopoeial
4metabolites
Celecoxib structure
Parent API

Celecoxib

CAS
169590-42-5
Formula
C17H14F3N3O2S
MW
381.4 g/mol
Code
ZX-003995

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

Pharmacopoeial3EP, USP, BP or JP named impurities
Metabolites4Hydroxy, desmethyl and conjugated forms

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

All Celecoxib reference materials

1–30 of 30 standards
Questions

Celecoxib impurities, answered

How many Celecoxib impurity standards does Zemixal list?
The catalogue currently lists 30 compounds for Celecoxib, including 3 pharmacopoeial impurities and 4 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 Celecoxib 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 Celecoxib 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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