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Raw material and ingredient selection; control of thermal conditions during rocessing; prolonged heating that under certain conditions may lead to accelerated elimination. Choice of appropriate storage conditions (avoiding excess temperature) over product shelf life where this is product relevant. HMF at very high concentrations is cytotoxic, causes irritation to the eyes, upper respiratory tract, skin, and mucus membranes. The available in vitro data generated in cellular systems suggests that HMF does not pose a serious risk to human health, but some concerns have been raised in conjunction with the potential genotoxic properties of speci c metabolites. European quality standards and Codex Alimentarius allow a maximum of 40 mg/kg HMF in honey. The fruit juice industry has set a standard value of 20 mg/kg as an upper limit for the product. Data on human dietary exposure is scarce. 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In principle, HMF can react further by decarboxylation, oxidation, dehydration, and polycondensation reactions (130, 153 155). Dehydration furnishes levulinic and formic acids. Small amounts of 5-hydroxymethyl-2-furan carboxylic acid (HMFA) are formed upon the oxidation of HMF. Durham et al. (90) have reported the formation of 5-hydroxymethylfuroic acid and furan-2,5dicarboxylic acid by HMF decomposition under autoclaving conditions. 2(2 hydroxyacetyl)-furan is formed as a side-product of fructose degradation and by condensation of both compounds in the presence of only catalytic amounts of amino compounds, leading to the formation of colored products. Self-condensation of HMF affords the corresponding ether. Studies of the decomposition of glucose, 13C-labeled in positions 1 and 6, under Curie-point pyrolysis conditions at 300 C, allow the speci c incorporation of the label into. 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