Furosemide impurity standards
For Furosemide, the Zemixal catalogue holds 15 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 6 pharmacopoeial impurities, 1 nitrosamine, 1 isotope-labelled standard, 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. For nitrosamine risk evaluation, the N-nitroso standards allow confirmatory LC-MS testing against the acceptable intake limits.
By impurity type
Counts are based on product names. One compound can fall into more than one type.