Zolmitriptan impurity standards
For Zolmitriptan, the Zemixal catalogue holds 19 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 6 pharmacopoeial impurities, 1 metabolite or hydroxylated analogue and 1 degradation product.
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
Counts are based on product names. One compound can fall into more than one type.
All Zolmitriptan reference materials
- CAS
- 191864-24-1
- Formula
- C19H25N3O4
- MW
- 359.4 g/mol
- CAS
- 251451-31-7
- Formula
- C14H14N2O4
- MW
- 274.27 g/mol