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CAS 528-16-5

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D-Glucopyranuronic acid

Description:
D-Glucopyranuronic acid, with the CAS number 528-16-5, is a naturally occurring uronic acid derived from glucose. It is characterized by its six-membered pyranose ring structure, which contains a carboxylic acid functional group at the C6 position, converting the hydroxymethyl group of glucose into a carboxyl group. This modification imparts unique properties, such as increased solubility in water and the ability to participate in various biochemical reactions. D-Glucopyranuronic acid plays a significant role in the metabolism of carbohydrates and is involved in the synthesis of glycosaminoglycans, which are essential components of connective tissues. It is also a key player in the detoxification processes in the liver, where it conjugates with various substances to facilitate their excretion. The compound is typically found in its anionic form at physiological pH, contributing to its biological activity. Its derivatives are utilized in pharmaceuticals and biochemistry, highlighting its importance in both natural and synthetic applications.
Formula:C6H10O7
InChI:InChI=1/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6?/m0/s1
InChI key:InChIKey=AEMOLEFTQBMNLQ-AQKNRBDQSA-N
SMILES:C(O)(=O)[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1
Synonyms:
  • <span class="text-smallcaps">D</span>-Glucopyranuronic acid
  • Glucopyranuronic acid, <span class="text-smallcaps">D</span>-
  • Hexopyranuronic Acid
  • NSC 165
  • D-Glucopyranuronic acid
  • Glucopyranuronic acid, D-
  • Carvedilol-d3 N&rsquo
  • (2S,3S,4S,5R)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid
  • Einecs 208-429-7
  • 3β,4α,5β,6α-Tetrahydroxytetrahydro-2H-pyran-2α-carboxylic acid
  • See more synonyms
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