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Xylonic Acid
Xylonic acid is a sugar acid that can be obtained by oxidation of the hemiacetal/aldehyde group of xylose. The C-2 epimer is known as lyxonic acid. References [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sugar Acid
A Sugar acid or acidic sugar is a monosaccharide with a carboxyl group at one end or both ends of its chain. Main classes of sugar acids include: * Aldonic acids, in which the aldehyde group (−CHO) located at the initial end ( position 1) of an aldose is oxidized. * Ulosonic acids, in which the −CH2(OH) group at the initial end of a 2-ketose is oxidized creating an α-ketoacid. * Uronic acids, in which the −CH2(OH) group at the terminal end of an aldose or ketose is oxidized. * Aldaric acids, in which both ends (−CHO and −CH2(OH)) of an aldose are oxidized. Examples Examples of sugar acids include: * Aldonic acids ** Glyceric acid (3C) ** Xylonic acid (5C) ** Gluconic acid (6C) ** Ascorbic acid (6C, unsaturated lactone) * Ulosonic acids ** Neuraminic acid (5-amino-3,5-dideoxy-D- ''glycero''-D- ''galacto''-non-2-ulosonic acid) ** Ketodeoxyoctulosonic acid (KDO or 3-deoxy-D- ''manno''-oct-2-ulosonic acid) * Uronic acids ** Glucuronic acid (6C) ** Galacturonic acid (6C) * ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Xylose
Xylose ( grc, ξύλον, , "wood") is a sugar first isolated from wood, and named for it. Xylose is classified as a monosaccharide of the aldopentose type, which means that it contains five carbon atoms and includes an aldehyde functional group. It is derived from hemicellulose, one of the main constituents of biomass. Like most sugars, it can adopt several structures depending on conditions. With its free aldehyde group, it is a reducing sugar. Structure The acyclic form of xylose has chemical formula . The cyclic hemiacetal isomers are more prevalent in solution and are of two types: the pyranoses, which feature six-membered rings, and the furanoses, which feature five-membered rings (with a pendant group). Each of these rings is subject to further isomerism, depending on the relative orientation of the anomeric hydroxy group. The dextrorotary form, -xylose, is the one that usually occurs endogenously in living things. A levorotary form, -xylose, can be synthesize ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sugar Acids
A Sugar acid or acidic sugar is a monosaccharide with a carboxyl group at one end or both ends of its chain. Main classes of sugar acids include: * Aldonic acids, in which the aldehyde group (−CHO) located at the initial end ( position 1) of an aldose is oxidized. * Ulosonic acids, in which the −CH2(OH) group at the initial end of a 2-ketose is oxidized creating an α-ketoacid. * Uronic acids, in which the −CH2(OH) group at the terminal end of an aldose or ketose is oxidized. * Aldaric acids, in which both ends (−CHO and −CH2(OH)) of an aldose are oxidized. Examples Examples of sugar acids include: * Aldonic acids ** Glyceric acid (3C) ** Xylonic acid (5C) ** Gluconic acid (6C) ** Ascorbic acid (6C, unsaturated lactone) * Ulosonic acids ** Neuraminic acid (5-amino-3,5-dideoxy-D- ''glycero''-D- ''galacto''-non-2-ulosonic acid) ** Ketodeoxyoctulosonic acid (KDO or 3-deoxy-D- ''manno''-oct-2-ulosonic acid) * Uronic acids ** Glucuronic acid (6C) ** Galacturonic acid (6C) * ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
