D-Glucuronic acid, 10G

SKU:
G5269-10G
$126.00

Description

D-Glucuronic acid ≥98% (GC), 10G

Synonym: Glucosiduronic acid

  • CAS Number 6556-12-3

     

  • Empirical Formula (Hill Notation) C6H10O7

     

  • Molecular Weight 194.14

     

  •  Beilstein/REAXYS Number 1727083

     

  •  EC Number 229-486-4

     

  •  MDL number MFCD00077778

     

  •  PubChem Substance ID 24895203

     

  •  NACRES NA.25

Properties

Related Categories β-Glucuronidase (beta-Glucuronidase), Acacia, Analytical and Industrial Enzymes, Biochemicals and Reagents, Carbohydrates,
Carbohydrates A to Z, Carbohydrates G, Cell Biology, D to K, Enzyme Inhibitors, Enzyme Inhibitors by Enzyme, Enzymes, Inhibitors, and Substrates, Glucuronidase, beta, Glycobiology, Inhibitors, Inhibitors and Substrates, Linum usitatissimum (Flax), Molecular Biology, Monosaccharide, Nutrition Research, Panax ginseng, Phytochemicals by Plant (Food/Spice/Herb), Post-Translational Modification, Proteomics, Related Products, Vaccinium macrocarpon (Cranberry)
Quality Level 200
biological source synthetic (organic)
assay ≥98% (GC)
form powder
optical activity [α]/D 35 to 37°, c = 6% (w/v) in H2O (equilibrium value)
application(s)  gas chromatography (GC): suitable
mp 159-161 °C (lit.)
solubility H2O: soluble 100 mg/mL, clear to slightly hazy
storage temp. room temp
SMILES string O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O
InChI 1S/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 AEMOLEFTQBMNLQ-QIUUJYRFSA-N

General description

Glucuronic acid is one of the component of xylan backbone, a hemicellulose present in plant cell wall.[4]

Application

D-Glucuronic acid has been used:
• in in vitro human digestion model[5]
• as a fibrous cellulose powder, to test the feeding preference among experimental termites[6]
• as a standard to quantify glucuronic acid in urine sample[7]

Packaging

10 mg in glass bottle

10, 25, 50, 100 g in poly bottle

Biochem/physiol Actions

In humans, glucuronic acid conjugation with steroidal compounds and drugs is an important step in phase II metabolic reactions. This influences the biotransformation process of the compound.

Safety Information

Personal Protective Equipment 
Eyeshields, Gloves, type N95 (US)
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
RTECS 
LZ8836600
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable