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K4125

Sigma-Aldrich

5-Keto-D-gluconic acid potassium salt

≥98.0% (TLC)

Synonym(s):

D-Xylo-5-hexulofuranosonic acid potassium salt

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1 G
PLN 936.00
5 G
PLN 3,720.00

PLN 936.00

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1 G
PLN 936.00
5 G
PLN 3,720.00

About This Item

Empirical Formula (Hill Notation):
C6H9KO7
CAS Number:
91446-96-7
Molecular Weight:
232.23
Beilstein:
3919618
MDL number:
MFCD00069562
UNSPSC Code:
12352201
PubChem Substance ID:
24896239
NACRES:
NA.25

PLN 936.00

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

300

Assay

≥98.0% (TLC)

form

powder

technique(s)

thin layer chromatography (TLC): suitable

impurities

≤10.0% water (Karl Fischer)

color

white

solubility

water: ~50 g/L

storage temp.

2-8°C

SMILES string

[K+].OCC(=O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O

InChI

1S/C6H10O7.K/c7-1-2(8)3(9)4(10)5(11)6(12)13;/h3-5,7,9-11H,1H2,(H,12,13);/q;+1/p-1/t3-,4+,5-;/m1./s1

InChI key

GSFHMOMWXNDPMM-YMDUGQBDSA-M

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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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000348127
0000340730
0000187245
0000340730
0000187245

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D-Gluconic acid solution 49-53 wt. % in H2O

Sigma-Aldrich

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D-Gluconic acid solution

Cycloheximide from microbial, ≥94% (TLC)

Sigma-Aldrich

C7698

Cycloheximide

Mustafa Elfari et al.
Applied microbiology and biotechnology, 66(6), 668-674 (2005-03-01)
Gluconobacter oxydans converts glucose to gluconic acid and subsequently to 2-keto-D-gluconic acid (2-KGA) and 5-keto-D-gluconic acid (5-KGA) by membrane-bound periplasmic pyrroloquinoline quinone-dependent and flavin-dependent dehydrogenases. The product pattern obtained with several strains differed significantly. To increase the production of 5-KGA
V S Saravanan et al.
Chemosphere, 66(9), 1794-1798 (2006-09-08)
Gluconacetobacter diazotrophicus an endophytic diazotroph also encountered as rhizosphere bacterium is reported to possess different plant growth promoting characteristics. In this study, we assessed the zinc solubilizing potential of G. diazotrophicus under in vitro conditions with different Zn compounds using
Marcel Merfort et al.
Applied microbiology and biotechnology, 73(2), 443-451 (2006-07-06)
Gluconobacter oxydans DSM 2343 is known to catalyze the oxidation of glucose to gluconic acid, and subsequently, to 2-keto-D-gluconic acid (2-KGA) and 5-keto-D-gluconic acid (5-KGA), by membrane-bound and soluble dehydrogenases. In G. oxydans MF1, in which the membrane-bound gluconate-2-dehydrogenase complex
Tuomas Salusjärvi et al.
Applied microbiology and biotechnology, 66(6), 664-667 (2004-11-27)
The chromosomal locus NP_636946 of Xanthomonas campestris DSM 3586 (ATCC 33913) which was earlier presumed to encode a quinoprotein glucose dehydrogenase has been cloned, expressed in Escherichia coli and the recombinant enzyme has been characterised. It was found to have
Ittipon Saichana et al.
Applied and environmental microbiology, 75(13), 4240-4247 (2009-05-05)
We isolated thermotolerant Gluconobacter strains that are able to produce 5-keto-d-gluconic acid (5KGA) at 37 degrees C, a temperature at which regular mesophilic 5KGA-producing strains showed much less growth and 5KGA production. The thermotolerant strains produced 2KGA as the major
View All Related Papers

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