A dedicated ion-pair HPLC column for furosine determination in dairy products – ensure milk quality and detect overheating damage with industry-standard precision.
CromSil™ Furo is a specialized reversed-phase HPLC column designed for the quantification of furosine, a key marker of heat-induced protein degradation in foods (especially dairy). Furosine (ε-furoylmethyl-lysine) is formed during the Maillard reaction when lactose reacts with lysine in milk proteins; its presence indicates the extent of overprocessing or overheating in milk powder, cheese, and infant formula. The purpose of CromSil™ Furo is to provide laboratories with a turn-key solution to measure this parameter accurately and efficiently, helping ensure product quality and compliance with international standards. Traditional column setups can struggle with furosine because it’s a polar, non-volatile amino acid derivative – CromSil™ Furo solves this problem by using a tailored C18 chemistry compatible with ion-pairing reagents to retain and separate furosine with high resolution. The result is a clear, reliable furosine peak that enables dairy producers and food testing labs to assess heat damage, nutritional value preservation, and compliance with the ISO 18329:2004 reference method for furosine determination. This product page outlines how CromSil™ Furo delivers scientific precision (meeting stringent method requirements) and commercial benefit (streamlining a complex analysis into a routine test).
CromSil™ Furo leverages column technology that is purpose-built for the ISO 18329:2004 (IDF 193) method – the official procedure for determining furosine in milk and dairy products. Technologically, it is a high-purity silica based C18 reversed-phase column optimized for use with ion-pair chromatography. The stationary phase is densely bonded with C18 (octadecyl) ligands, providing a hydrophobic matrix to separate furosine from other matrix components. An ion-pairing reagent added to the mobile phase (per the standard method, typically an alkylsulfonate or similar) forms a transient pair with the polar furosine molecule, rendering it more hydrophobic so it can interact strongly with the C18 phase. This allows furosine, which would normally elute early, to be retained longer and resolved from interfering substances. The column is engineered with an appropriate pore size and surface area to handle the slightly larger size of furosine (a derivatized amino acid) and similar matrix peptides without sacrificing efficiency.
Crucially, CromSil™ Furo is tested to ensure it produces the specified furosine retention time and peak shape under the ISO method conditions. The typical setup uses an ion-pair buffer (e.g., a mixture of an organic acid and an ion-pair reagent) and UV detection at 280 nm. This column’s silica is ultra-high purity to minimize any silanol interactions or ghost peaks, leading to a very stable baseline and symmetric furosine peak even with UV detection at 280 nm. By utilizing a dedicated bonded phase and rigorous QA, the CromSil™ Furo column achieves the sensitivity and specificity needed to detect furosine at low levels (which can be in the low ppm in products). The technology marries the reliability of a validated method with enhancements that make the column more robust – for instance, special end-capping to reduce tailing of basic amino compounds, and a dimension that balances analysis time with resolution (generally a 250 mm length to fully resolve furosine from closely eluting amino acids or lactose). In summary, the column’s background is an ion-pair reversed-phase system offering targeted performance for furosine, aligning with scientific standards and ensuring that laboratories can trust the results for critical quality decisions.
While CromSil™ Furo is specialized, it has vital applications in food quality and nutritional analysis:
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