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Impurity reference standards

Lenalidomide impurity standards

This page brings together 58 Lenalidomide related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. The range includes 3 metabolites or hydroxylated analogues.

58reference materials
3metabolites
Lenalidomide structure
Parent API

Lenalidomide

CAS
191732-72-6
Formula
C13H13N3O3
MW
259.26 g/mol
Code
ZX-004217

Each lot ships with a certificate of analysis, and characterisation data such as 1H-NMR, mass spectrum and HPLC purity can be shared before you order. 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

Metabolites3Hydroxy, desmethyl and conjugated forms

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

All Lenalidomide reference materials

1–58 of 58 standards
Questions

Lenalidomide impurities, answered

What Lenalidomide reference materials are available?
The catalogue currently lists 58 compounds for Lenalidomide, including 3 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 Lenalidomide 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 Lenalidomide 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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