| CAS Number | 17924-92-4 |
|---|---|
| Molecular Formula | C18H22O5 |
| Molecular Weight | 318.369 |
| InChI Key | MBMQEIFVQACCCH-QBODLPLBSA-N |
| LogP | 3.49 |
| Synonyms |
|
Applications:
Uv-Vis Spectrum of Zearalenone
March 26, 2026
Access the UV-Vis Spectrum SIELC Library

If you are looking for optimized HPLC method to analyze Zearalenone check our HPLC Applications library
For optimal results in HPLC analysis, it is recommended to measure absorbance at a wavelength that matches the absorption maximum of the compound(s) being analyzed. The UV spectrum shown can assist in selecting an appropriate wavelength for your analysis. Please note that certain mobile phases and buffers may block wavelengths below 230 nm, rendering absorbance measurement at these wavelengths ineffective. If detection below 230 nm is required, it is recommended to use acetonitrile and water as low UV-transparent mobile phases, with phosphoric acid and its salts, sulfuric acid, and TFA as buffers.
For some compounds, the UV-Vis Spectrum is affected by the pH of the mobile phase. The compound was dissolved in Acetonitrile.
HPLC Analysis of Zearalenone and Ochratoxin A on Primesep B2 Mixed-Mode Column
May 11, 2015

Zearalenone and Ochratoxin A are harmful mycotoxins commonly found in grains and other foods. They were separated using the Primesep B2 reversed-phase anion-exchange mode column. Retention can be controlled by adjusting concentration of both acetonitrile and buffer.
| Column | Primesep B2, 4.6×150 mm, 5 µm, 100A |
| Mobile Phase | MeCN/H2O |
| Buffer | Formic Acid |
| Flow Rate | 1.0 ml/min |
| Detection | UV, 250 nm |
| Class of Compounds |
Base, Acid, Hydrophilic, Ionizable |
| Analyzing Compounds | Zearalenone, Ochratoxin A |
Application Column
Primesep B2
Column Diameter: 4.6 mm
Column Length: 50 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended
Zearalenone
UV Detection

