Zirconyl chloride upon hydrolysis in water to form Zr(OH) Ο© has been found to react to form a fluorescent derivative with not only a ketose such as fructose but also a hexose such as glucose and the disaccharide sucrose. When reaction conditions such as a temperature of 99Β°C and a time of 60 min are used, detection limits below 1 g/mL are possible. All three zirconyl-sugar derivatives show very similar absorbance and fluorescence spectra, indicating a common mechanism involving formation of an enediol which can be complexed with ZrOH Ο© is likely. Because the reactivity order is glucose Ο½ sucrose Ο½ fructose, the reaction can be made selective for fructose at a lower reaction temperature and time such as 60Β°C at 5 min. Because interference from ascorbic acid and caffeine is also avoided, the fluorescent determination of fructose in soft drink samples after simply a dilution step is possible. We have also employed this reaction for flow injection analysis (FIA) using a polystyrene-divinylbenzene-packed HPLC column as a mixing device. Using a 0.01 M HClO 4 with 1% zirconyl chloride carrier, we obtained a linear calibration curve from 2 to 30 g/mL with a correlation coefficient of 0.994. A detection limit less than 2 g/mL was possible. A comparison of results for the FIA of soft drinks with the enzymatic method involving fructose-5-dehydrogenase confirmed the FIA method was quite specific for fructose.