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642-99-9

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642-99-9 Usage

Definition

ChEBI: The D-stereoisomer of mannonic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 642-99-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 642-99:
(5*6)+(4*4)+(3*2)+(2*9)+(1*9)=79
79 % 10 = 9
So 642-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-5,7-11H,1H2,(H,12,13)/p-1/t2-,3-,4+,5+/m1/s1

642-99-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name D-galactonic acid

1.2 Other means of identification

Product number -
Other names d-Galaktonsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:642-99-9 SDS

642-99-9Relevant articles and documents

Preparation method of gluconic acid

-

Paragraph 0009; 0021; 0024-0059, (2019/06/05)

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

Tomar, Ravi,Sharma, Jatin,Nishimura, Shun,Ebitani, Kohki

supporting information, p. 843 - 845 (2016/07/16)

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.

Biomass Oxidation: Formyl C-H Bond Activation by the Surface Lattice Oxygen of Regenerative CuO Nanoleaves

Amaniampong, Prince N.,Trinh, Quang Thang,Wang, Bo,Borgna, Armando,Yang, Yanhui,Mushrif, Samir H.

supporting information, p. 8928 - 8933 (2015/08/03)

An integrated experimental and computational investigation reveals that surface lattice oxygen of copper oxide (CuO) nanoleaves activates the formyl C-H bond in glucose and incorporates itself into the glucose molecule to oxidize it to gluconic acid. The reduced CuO catalyst regains its structure, morphology, and activity upon reoxidation. The activity of lattice oxygen is shown to be superior to that of the chemisorbed oxygen on the metal surface and the hydrogen abstraction ability of the catalyst is correlated with the adsorption energy. Based on the present investigation, it is suggested that surface lattice oxygen is critical for the oxidation of glucose to gluconic acid, without further breaking down the glucose molecule into smaller fragments, because of C-C cleavage. Using CuO nanoleaves as catalyst, an excellent yield of gluconic acid is also obtained for the direct oxidation of cellobiose and polymeric cellulose, as biomass substrates.

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