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Fructose in sucrose

Why do you suppose that the major form of D-fructose in solution is the pyranose form but D-fructose in sucrose is in the furanose form ... [Pg.196]

Common sugars, such as glucose, fructose, and sucrose, in a wide variety of foods can be determined after dilution and filtration before HPAEC-PAD analysis. Such foods include tomato ketchup, butterscotch candy, and chocolate (Dionex Technical Manual, 1995). Sample preparation for the high-fat chocolate include supercritical fluid extraction to remove the fat. Impurities in sweeteners can be detected, such as glucose and fructose in sucrose. [Pg.505]

The concentrations of nine sugars (fucose, methylglucose, arabinose, glucose, fructose, lactose, sucrose, cellobiose, and maltose) in beer, milk, and soda are determined using an... [Pg.614]

Sucrose (Section 25.14) A disaccharide of glucose and fructose in which the two monosaccharides are joined at their anomeric positions. [Pg.1294]

Disaccharides, which are dimers farmed when two monosaccharide units combine with the elimination of H20. The monosaccharides may be the same (two glucose units in maltose) or different (a glucose and fructose unit in sucrose). [Pg.617]

Sucrose, the compound we call sugar, is the most common disaccharide. One of the monomer units in sucrose is a-glucose. The other is fructose, a monosaccharide found in honey and natural fruit juices. [Pg.618]

Sucrose can, however, degrade to D-glucose and D-fructose in slightly alkaline solution at pH up to 8.3 (sucrose is most stable611 at pH 8.3-8.5, although the reason for this requires some elucidation), but this degradation proceeds by the normal acid-hydrolysis mechanism. In sucrose manufacture, therefore, the main reaction causing sucrose loss, between pH 7 and about 8.3, is the same acid hydrolysis that occurs at lower (acid) pH. [Pg.449]

Fig. 1 (A) Chromatographic separation of sugars. Track 1 fructose, 2 sucrose, 3 glucose, 4 mixture of the substances in tracks 1-3, 5 mixture of substances in tracks 1-3 and 6, 6 Fructo-oligosaccharides, 7 1-kestose, 8 mixture of glucose, maltose, maltotriose and maltotetraose. (B) Absorption scan of track 5 with 200 ng each substance per chromatogram zone 1 = fructosyl-nystose, 2 = nystose, 3 = 1-kestose, 4 = fructose, 5 = sucrose, 6 = glucose. Fig. 1 (A) Chromatographic separation of sugars. Track 1 fructose, 2 sucrose, 3 glucose, 4 mixture of the substances in tracks 1-3, 5 mixture of substances in tracks 1-3 and 6, 6 Fructo-oligosaccharides, 7 1-kestose, 8 mixture of glucose, maltose, maltotriose and maltotetraose. (B) Absorption scan of track 5 with 200 ng each substance per chromatogram zone 1 = fructosyl-nystose, 2 = nystose, 3 = 1-kestose, 4 = fructose, 5 = sucrose, 6 = glucose.
Carbohydrates are an important food source for most organisms. Glucose, fructose, and sucrose are small carbohydrate molecules that can be broken down rapidly to provide quick energy for cells. Large amounts of energy are stored in carbohydrate macromolecules called polysaccharides. For example, glycogen is a polysaccharide used... [Pg.919]

GC/MS. A large number of DFAs were identified but their compositions and amounts depend on the nature of sugar used for caramelization. Fructose caramel contains the highest amount of DFAs (more than 39% of dry matter), while glucose caramel contains mainly glucobioses. In sucrose caramel, both types of compounds were found in similar proportions. Based on these observations, DAFs are considered suitable tracers for the determination of caramel authenticity. ... [Pg.338]

In an fermentation process of a solution containing sucrose, the enzyme in-vertase, present in yeast, acts as a catalyst to convert sucrose into a 1 1 mixture of glucose and fructose. Thus, sucrose is a disaccharide that hydrolyzes in the presence of certain bacteria to yield glucose and fructose. The ether linkage in sucrose is broken to yield two alcohols ... [Pg.176]

Invert sugar is only encountered as a syrup. The fructose in the mixture will not crystallise so attempts to crystallise invert sugar yield dextrose. Invert sugar overcomes one of the big drawbacks of sucrose. Invert... [Pg.105]

The enzymatic synthesis of sucrose also throws light on the formation of the furanose form of fructose in the sucrose molecule. The fact that sucrose is directly formed from D-glucose-l-phosphate and D-fructose supports Isbell and Pigman s34 and Gottschalk s85 evidence that the latter monosaccharide occurs in solution in an equilibrium mixture of furanose and pyranose forms. This makes it unnecessary to postulate a special mechanism of stabilization of a five membered (furanose) ring before the formation of compound sugars containing the D-fructose molecule.86... [Pg.52]

Glucose is the simplest carbohydrate. It is found in grapes and corn syrup. Fructose gives fruit its sweet taste. A condensation reaction between glucose and fructose produces sucrose, commonly called table sugar. Sucrose is found in sugar cane and sugar beets. [Pg.90]

Genetic deficiency of fructokinase is benign and often detected incidentally when the urine is checked for glucose with a dipstick. Fructose 1-phosphate aldolase deficiency is a severe disease because of accumulation of fructose 1-phosphate in the liver and renal proximal tubules. Table 1-12-4 compares the two conditions. Symptoms are reversed after removing fructose and sucrose from the diet. [Pg.172]

Thermolysis of D-fructose in acid solution provides 11 and 2-(2-hydrox-yacetyl)furan (44) as major products. Earlier work had established the presence of 44 in the product mixtures obtained after acid-catalyzed dehydrations of D-glucose and sucrose. Eleven other products were identified in the D-fructose reaction-mixture, including formic acid, acetic acid, 2-furaldehyde, levulinic acid, 2-acetyl-3-hydroxyfuran (isomaltol), and 4-hydroxy-2-(hydroxymethyl)-5-methyl-3(2//)-furanone (59). Acetic acid and formic acid can be formed by an acid-catalyzed decomposition of 2-acetyl-3-hydroxyfuran, whereas levulinic acid is a degradation prod-uct of 11. 2,3-Dihydro-3,5-dihydroxy-6-methyl-4//-pyran-4-one has also been isolated after acid treatment of D-fructose.The pyranone is a dehydration product of the pyranose form of l-deoxy-D-eo f o-2,3-hexodiulose. In aqueous acid seems to be the major reaction product of the pyranone. [Pg.286]


See other pages where Fructose in sucrose is mentioned: [Pg.223]    [Pg.38]    [Pg.105]    [Pg.59]    [Pg.223]    [Pg.38]    [Pg.105]    [Pg.59]    [Pg.368]    [Pg.999]    [Pg.32]    [Pg.33]    [Pg.223]    [Pg.232]    [Pg.449]    [Pg.45]    [Pg.167]    [Pg.41]    [Pg.256]    [Pg.206]    [Pg.69]    [Pg.121]    [Pg.48]    [Pg.202]    [Pg.107]    [Pg.108]    [Pg.52]    [Pg.73]    [Pg.74]    [Pg.45]    [Pg.46]    [Pg.47]    [Pg.47]    [Pg.48]    [Pg.56]    [Pg.88]    [Pg.35]   
See also in sourсe #XX -- [ Pg.1058 ]




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