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Galactose acid

NMR spectra have shown that ethanol-water and water extract at Galium ver-um, Rubia tinctorum, Hypericum perforatum and Humulus lupulus contain sugar alcohols (myoinositol, arabitol, lybitol, inositol), and monosaccharides (glucose, xylose, ribose, fractose, galactose. Acids, such as citric, malonic, mahc, glucuronic are also present. For more details see [47]. [Pg.287]

They are found in a great variety of plants and are strong fish poisons. On hydrolysis they yield a variety of sugars, frequently several molecules to each aglucone. Glucose, galactose, arabinose are the more common pentoses, methylpentoses and glucuronic acid are also obtained. [Pg.352]

Vigorous oxidation of a monosaccharide (e.g., with dUute nitric acid) produces carboxyl groups at both ends of the chain. Thus galactose gives the sparingly soluble mucic acid glucose affords the soluble saccharic acid, which is best isolated as the sparingly soluble acid potassium salt. [Pg.452]

COoH Saccharic acid 1 CHjOH Galactose 1 COjH Mucic acid... [Pg.452]

Disaccharides, e.g., lactose, which yield galactose upon hydrolysis, will also give the sparingly-soluble mucic acid but in poorer 3deld. This reaction may be employed for the differentiation between certain disaccharides lactose — mucic + saccharic acids sucrose — saccharic acid only maltose — saccharic acid only. [Pg.453]

D-Galactose (hydrated) D-Galactose (anhydrous). 1201 170 + 82 201 15-19 Penta-acetate, a- 95, P- 142 inucic acid, 213... [Pg.457]

Oxidation of galactose (or a galactose-containing sugar) to mucic acid. Dissolve 1 g. of galactose or lactose in a mixture of 10 ml. of water and 5 ml. of concentrated nitric acid contained in a small evaporating dish, and evaporate the solution to dryness on a water bath. Stir the cold residue with 10 ml. of cold water, filter off the mucic acid, wash it with cold water, dry and determine the m.p. (212-213° with decomposition). [Pg.1070]

D (+) Galactose is a constituent of numerous polysaccharides It is best obtained by acid hydrolysis of lactose (milk sugar) a disaccharide of d glucose and d galactose L (—) Galactose also occurs naturally and can be prepared by hydrolysis of flaxseed gum and agar The principal source of d (+) mannose is hydrolysis of the polysaccharide of the ivory nut a large nut like seed obtained from a South American palm... [Pg.1032]

The structure of compound A was established in part by converting it to known compounds Treat ment of A with excess methyl iodide in the presence of silver oxide followed by hydrolysis with dilute hydrochlonc acid gave a tnmethyl ether of D galactose Companng this trimethyl ether with known trimethyl ethers of D galactose allowed the structure of compound A to be deduced... [Pg.1068]

Gum ghatti is the calcium and magnesium salt of a complex polysaccharide which contains L-arabinose, D-galactose, D-mannose, and D-xylose and D-glucuronic acid (48) and has a molecular weight of approximately 12,000. On dispersion in water, gum ghatti forms viscous solutions of viscosity intermediate between those of gum arabic and gum karaya. These dispersions have emulsification and adhesive properties equivalent to or superior to those described for gum arabic. [Pg.434]

Another microbial polysaccharide-based emulsifier is Hposan, produced by the yeast Candida lipolytica when grown on hydrocarbons (223). Liposan is apparentiy induced by certain water-immiscible hydrocarbons. It is composed of approximately 83% polysaccharide and 17% protein (224). The polysaccharide portion consists of D-glucose, D-galactose, 2-amino-2-deoxy-D-galactose, and D-galacturonic acid. The presence of fatty acyl groups has not been demonstrated the protein portion may confer some hydrophobic properties on the complex. [Pg.298]

In all plants and most animals, L-ascorbic acid is produced from D-glucose (4) and D-galactose (26). Ascorbic acid biosynthesis in animals starts with D-glucose (4). In plants, where the biosynthesis is more compHcated, there are two postulated biosynthetic pathways for the conversion of D-glucose or D-galactose to ascorbic acid. [Pg.18]

Oxidation of tiie caibon atoms at both ends of the carbon chain produces an aldaric acid. That made from D-galactose is galactaric acid [526-99-8] a... [Pg.479]

Principal polysaccharide constituent listed. Sugars are D- unless otherwise noted. Ara = arabinose Gal = galactose GalA = galacturonic acid ... [Pg.73]


See other pages where Galactose acid is mentioned: [Pg.197]    [Pg.272]    [Pg.550]    [Pg.875]    [Pg.189]    [Pg.434]    [Pg.434]    [Pg.434]    [Pg.32]    [Pg.33]    [Pg.298]    [Pg.370]    [Pg.386]    [Pg.49]    [Pg.5]    [Pg.18]    [Pg.19]    [Pg.19]    [Pg.387]    [Pg.91]    [Pg.179]    [Pg.484]    [Pg.400]    [Pg.2135]    [Pg.661]    [Pg.662]    [Pg.666]    [Pg.742]    [Pg.1032]    [Pg.271]    [Pg.227]    [Pg.234]   
See also in sourсe #XX -- [ Pg.350 , Pg.353 , Pg.354 , Pg.359 , Pg.360 , Pg.366 ]




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Galactose ascorbic acid synthesis

Galactose lactic acid bacteria

Galactose oxidation to mucic acid

Galactose rich acidic glycoprotein

Mucic acid galactose

Pectic acid galactose units

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