C 6 H 10 O 7 (194.14). Abbreviated as GlcU. D -Glucuronic acid is widely distributed in the animal and plant kingdoms as a component of mucopolysaccharides such as chondroitin sulfate, heparin, and hyaluronic acid, and polysaccharides such as gum arabic and wheat straw. It exists in small amounts in free form in blood and urine. It can be obtained in various ways, such as hydrolysis of plant gums, mucilages, and glycosides, partial reduction of D -glucaric acid-1,4-lactone, and oxidation of 1,2,3,4-tetra- O -acetyl- D -glucopyranose. The β-anomer has a melting point of 165 °C. +11.7 → +36.3° (water). p K a 3.18. Soluble in water and ethanol. It shows general properties of a reducing sugar. When heated in hydrochloric acid, it decomposes into carbon dioxide and furfural. This reaction is used for detection and quantification. 3,6-Lactone C 6 H 8 O 6 (176.13) has a melting point of 176-178 °C. +20° (water). LD 50 10700 mg/kg (rat, oral). It is related to detoxification. When animals are administered poisons that are not easily oxidized in the body, such as camphor, chloral, and phenol, they become glycosides of D -glucuronic acid in the liver and are excreted in the urine. [CAS 6556-12-3][CAS 63-29-6:3,6-Lactone] Source: Morikita Publishing "Chemical Dictionary (2nd Edition)" Information about the Chemical Dictionary 2nd Edition |
C6H10O7(194.14).略号GlcU.D-グルクロン酸はコンドロイチン硫酸,ヘパリン,ヒアルロン酸などのムコ多糖類や,アラビアゴム,麦ワラなどの多糖類の構成成分として広く動物,植物界に分布している.血液や尿中には,微量ながら遊離状で存在する.植物性ゴム質,粘液質,配糖体の加水分解のほか,D-グルカル酸-1,4-ラクトンの部分還元,1,2,3,4-テトラ-O-アセチル-D-グルコピラノースの酸化など,種々の方法で得られる.β-アノマーは融点165 ℃.+11.7→+36.3°(水).pKa 3.18.水,エタノールに可溶.還元糖としての一般的性質を示す.塩酸中で加熱すると,二酸化炭素とフルフラールとに分解する.この反応は検出,定量に利用される.3,6-ラクトンC6H8O6(176.13)は融点176~178 ℃.+20°(水).LD50 10700 mg/kg(ラット,経口).解毒に関係があり,ショウノウ,クロラール,フェノールなど,体内で酸化されにくい毒物を動物に投与すると,それらは肝臓中でD-グルクロン酸の配糖体となり,尿中に排出される.[CAS 6556-12-3][CAS 63-29-6:3,6-ラクトン] 出典 森北出版「化学辞典(第2版)」化学辞典 第2版について 情報 |
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