7760-07-8

Basic information

• Product Name: Hexanoic acid, 2,3,4,5,6-pentahydroxy- (7CI, 8CI)
• Synonyms: Hexanoic acid, 2,3,4,5,6-pentahydroxy- (7CI, 8CI)
• CAS NO: 7760-07-8
• Molecular Formula: C₆H₁₂O₇
• Molecular Weight: 196.16
• Mol File: 7760-07-8.mol
• Article Data: 45

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Hexanoic acid, 2,3,4,5,6-pentahydroxy- (7CI, 8CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Hexanoic acid, 2,3,4,5,6-pentahydroxy- (7CI, 8CI)(7760-07-8)
• EPA Substance Registry System: Hexanoic acid, 2,3,4,5,6-pentahydroxy- (7CI, 8CI)(7760-07-8)

Safety Data

• Hazardous Substances Data: 7760-07-8(Hazardous Substances Data)

Upstream product

• 6027-89-0 L-gulose 
• 6556-12-3 D-Glucuronic acid 
• 76742-42-2 sodium D-lyxo-5-hexulosonate 
• 14984-34-0 sodium D-glucuronate 
• 87-79-6 L-sorbose 
• 74-90-8 hydrogen cyanide 
• 609-06-3 L-xylose 
• 1128-23-0 L-gulono-1,4-lactone 
• 74183-68-9 6-nitro-6-deoxy-D-glucitol 
• 50-99-7 D-glucose 
• 492-61-5 β-D-glucose 
• 1114-34-7 D-lyxose 
• 59-23-4 D-Galactose 
• 20246-35-9 talonic acid 

Downstream Products

• 29431-73-0 (3aS)-9anti-bromo-8syn-hydroxy-3a-methyl-(3ar,3bt,7ac)-octahydro-1t,6at-ethano-pentaleno[1,2-c]furan-1c,6t-dicarboxylic acid dimethyl ester 
• 108757-42-2 (1S,2R,3S,4R)-1-(5,6-dichloro-1H-benzo[d]imidazol-2-yl)pentane-1,2,3,4,5-pentaol 
• 157663-13-3 L-gluconic acid 
• 133-42-6 gluconic acid 
• 16752-03-7 D-galactonic acid methyl ester 
• 18336-97-5 d-galactonic acid-semicarbazide 
• 60662-25-1 D-galactonic acid ; lead (II)-compound with lead (II)-oxide 
• 6338-41-6 5-hydroxymethyl-furan-2-carboxylic acid 
• 20246-35-9 talonic acid 
• 1114-34-7 D-lyxose 
• 13532-38-2 γ-Hydroxycaproic acid 
• 2782-07-2 D-galactono-1,4-lactone 
• 15892-28-1 (3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-one 
• 65143-68-2 2,3,5,6-tetra-O-acetyl-D-glucono-1,4-lactone 

Relevant articles and documents

Preparation method of gluconic acid

The invention discloses a method for preparing gluconic acid from glucose as a raw material with a catalytic oxidation means. Gluconic acid is prepared through oxidation of glucose by an aqueous phasewith air or oxygen as an oxidizing agent and a transition metal compound and nitrous acid or nitrite as a composite catalyst. The reaction is simple in operation and mild in condition, the glucose conversion rate is high, the selectivity of the gluconic acid product is good, and the method has important application prospects.

Aqueous oxidation of sugars into sugar acids using hydrotalcite-supported gold nanoparticle catalyst under atmospheric molecular oxygen

Hydrotalcite-supported gold nanoparticles show good activity as a heterogeneous catalyst for the oxidation of monosaccharides (xylose, ribose, galactose and mannose) and disaccharides (lactose and cellobiose) into the corresponding sugar acids under external base-free conditions in water solvent using atmospheric pressure of molecular oxygen. The produced sugar acids were thoroughly identified by 1H-, 13C-, and HMQC-NMR and ESI-FT-ICR MS spectroscopic techniques.

Selective oxidation of uronic acids into aldaric acids over gold catalyst

Herein, uronic acids available from hemicelluloses and pectin were used as raw material for the synthesis of aldaric acids. Au/Al2O3 catalyst oxidized glucuronic and galacturonic acids quantitatively to the corresponding glucaric and galactaric acids at pH 8-10 and 40-60 °C with oxygen as oxidant. The pH has a significant effect on the initial reaction rate as well as desorption of acid from the catalyst surface. At pH 10, a TOF value close to 8000 h-1 was measured for glucuronic acid oxidation. The apparent activation energy Ea for glucuronic acid oxidation is dependent on the pH which can be attributed to the higher energy barrier for desorption of acids at lower pH. This journal is