61793
2-Keto-D-glucose
≥98.0% (TLC)
Synonim(y):
D-Glucosone
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Wybierz wielkość
100 MG
1060,00 zł
1060,00 zł
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C6H10O6
Numer CAS:
Masa cząsteczkowa:
178.14
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
Przejdź do
Pomoc techniczna
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Pozwól nam pomócInChI
1S/C6H10O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,4-6,8,10-12H,2H2/t4-,5-,6-/m1/s1
SMILES string
OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)C=O
InChI key
DCNMIDLYWOTSGK-HSUXUTPPSA-N
assay
≥98.0% (TLC)
form
solid
color
white to beige
storage temp.
2-8°C
Quality Level
1 of 4
Ta pozycja | |||
|---|---|---|---|
| assay ≥98.0% (TLC) | assay ≥99.0% (TLC) | assay ≥95.0% | assay ≥99.0% (TLC) |
| Quality Level 100, 200 | Quality Level 200 | Quality Level 100 | Quality Level 200 |
| form solid | form solid | form powder | form solid |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. - | storage temp. −20°C |
| color white to beige | color white | color - | color white |
Application
2-Keto-D-glucose (D-Glucosone) is a key intermediate of a secondary metabolic pathway leading to the antibiotic cortalcerone. D-Glucosone is a substrate that may be used to identify, differentiate and characterize hexokinase(s).
Biochem/physiol Actions
2-Keto-D-glucose is the key intermediate of a secondary metabolic pathway leading to the antibiotic β-pyrone cortalcerone.[1] This antibiotic offers protection to fungi against bacteria.[2] The enzymatic oxidation of d-glucose by pyanose 2 oxidase results in 2-keto-D-glucose,[2] and is considered as rare sugar.[3]
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Cellulose Chemistry and Properties: Fibers, Nanocelluloses and Advanced Materials, 178-178 (2016)
Model-based heuristic optimized operating policies for D-glucose oxidation in a batch reactor with pulsate addition of enzyme
Maria Gheorghe
Computers & Chemical Engineering, 31(10), 1231-1241 (2007)
Stefan Mittelmaier et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(11-12), 877-882 (2010-03-02)
Glucose degradation products (GDPs) formed during heat sterilization of peritoneal dialysis (PD) fluids exert cytotoxic effects and promote the formation of advanced glycation end-products in the peritoneal cavity. As a result, long-term application of continuous ambulatory peritoneal dialysis is limited.
A pH switch affects the steady-state kinetic mechanism of pyranose 2-oxidase from Trametes ochracea.
Kunchala Rungsrisuriyachai et al.
Archives of biochemistry and biophysics, 483(1), 10-15 (2009-01-17)
The flavin-dependent pyranose 2-oxidase catalyzes the oxidation of d-glucose and other pyranoses at the C2 atom to yield 2-keto-sugars and hydrogen peroxide. Here, the steady-state kinetic mechanism of the enzyme from Trametes ochracea was investigated as a function of pH.
Wenhui Zhang et al.
Journal of the American Chemical Society, 134(28), 11511-11524 (2012-06-02)
Pathways in the degradation of the C(6) 1,2-dicarbonyl sugar (osone) D-glucosone 2 (D-arabino-hexos-2-ulose) in aqueous phosphate buffer at pH 7.5 and 37 °C have been investigated by (13)C and (1)H NMR spectroscopy with the use of singly and doubly (13)C-labeled
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