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Maltitol structure

Fig. 3. Structures of disaccharide alcohols (a) maltitol, (b) lactitol, (c) a-D-glucopyraiiosyl-l,l-D-maiinitol(dihydrate), and (d)... Fig. 3. Structures of disaccharide alcohols (a) maltitol, (b) lactitol, (c) a-D-glucopyraiiosyl-l,l-D-maiinitol(dihydrate), and (d)...
Fig. 18.—Structure of Maltitol, Showing Multiple Hydrogen-bonding. " [Key , more acidic possible hydrogen-bond.]... Fig. 18.—Structure of Maltitol, Showing Multiple Hydrogen-bonding. " [Key , more acidic possible hydrogen-bond.]...
The separation and identification of disaccharides is often an important step in the elucidation of the structure of a natural polysaccharide, and Percival484 has published useful data on the O-trimethyl-silyl derivatives of a variety of disaccharides and their reduction products. In some instances, the trimethylsilyl ethers of the disaccharide alditols have lower retention times than those of the disaccharide derivatives. The per-O-trimethylsilyl derivatives of gentiobi-itol and maltitol were encountered in studies on the structure of Pneumococcus Type II capsular polysaccharide.4843... [Pg.69]

Maltitol (4-O-CC-D-glucopyranosyl-D-glucitol) formed by catalytic hydrogenation of maltose (97), has been obtained both as a noncrystalline powder and a viscous liquid (98). Structures of disaccharide alcohols are shown in Figure 3. [Pg.49]

In recent years disaccharide alcohols have become important. These include isomalt, maltitol, lactitol, and hydrogenated starch hydrolyzates (HSH). Maltitol is hydrogenated maltose with the structure shown in Figure 4-20. It has the highest sweetness of the disaccharidepolyols compared to sugar... [Pg.121]

Numerous laboratories have tackled the effect of a series of non-volatile plasticizo-s, such as glycerol [84, 87, 88, 89, 90, 93, 94], urea [84, 87], fructose [85], xylitol, sorbitol, maltitol [87, 90, 94], glycols (EG, TEG, PG, PEG) [84, 87, 89, 94], ethanolamine [92] and formamide [91]. Several criteria concerning the most appropriate structures for this key role have been put forward [94], although a rough first principle simply predicts that any substance capable of forming hydrogen bonds would be able to plasticize starch [95]. [Pg.329]

Figure 18.1. Chemical structures of D-mannitol, D-sorbitol, D-erythritol, 0-galactitol, D-xylitol, D-ribitol, D-lactitol, and D-maltitol. Figure 18.1. Chemical structures of D-mannitol, D-sorbitol, D-erythritol, 0-galactitol, D-xylitol, D-ribitol, D-lactitol, and D-maltitol.

See other pages where Maltitol structure is mentioned: [Pg.121]    [Pg.86]    [Pg.1129]    [Pg.209]    [Pg.1129]    [Pg.522]    [Pg.514]    [Pg.74]    [Pg.214]    [Pg.270]    [Pg.167]   
See also in sourсe #XX -- [ Pg.276 ]

See also in sourсe #XX -- [ Pg.45 , Pg.276 ]




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Maltitol

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