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The formation of 5-hydroxymethylfurfural from hexoses
Australian Journal of Chemistry, 1966In the acid catalysed conversion of hexoses to furans, the yield of 2- furyl hydroxymethyl ketone (FHK) relative to that of 5- hydroxymethylfurfural (HMF) is the same when either glucose or fructose is used as the starting material. The significance of this result is discussed in relation to the various reaction mechanisms proposed for the formation of
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5-Hydroxymethylfurfural mediated developmental toxicity in Drosophila melanogaster
Food and Chemical Toxicology5-hydroxymethylfurfural is a common byproduct in food. However, its effect on growth and development remains incompletely understood. This study investigated the developmental toxicity of 5-HMF to Drosophila larvae. The growth and development of Drosophila melanogaster fed with 5-50 mM 5-HMF was monitored, and its possible mechanism was explored.
Xunlin, Chen +6 more
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Acrylamid und 5‐Hydroxymethylfurfural in Trockenfrüchten
Lebensmittelchemie, 2023I. Richter +4 more
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Platinum Catalyzed Oxidation of 5-Hydroxymethylfurfural
1990The liquid phase oxidation of 5-hydroxymethylfurfural (HMF) over platinum on alumina catalysts is described. The main intermediate is 5-formyl-2-furan-carboxylic acid (FFCA), indicating that the hydroxymethyl group of HMF is oxidized first in the presence of the aldehyde group.
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Current Situation of the Challenging Scale‐Up Development of Hydroxymethylfurfural Production
ChemSusChem, 2020Catherine Rosenfeld +2 more
exaly