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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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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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

G1951

D-Gluconic acid solution

Cycloheximide from microbial, ≥94% (TLC)

Sigma-Aldrich

C7698

Cycloheximide

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
U Herrmann et al.
Applied microbiology and biotechnology, 64(1), 86-90 (2003-10-18)
For the conversion of glucose to 5-keto-D-gluconate (5-KGA), a precursor of the industrially important L-(+)-tartaric acid, Gluconobacter strains were genetically engineered. In order to increase 5-KGA formation, a plasmid-encoded copy of the gene encoding the gluconate:NADP-5 oxidoreductase (gno) was overexpressed
Kazunobu Matsushita et al.
Applied and environmental microbiology, 69(4), 1959-1966 (2003-04-05)
Acetic acid bacteria, especially Gluconobacter species, have been known to catalyze the extensive oxidation of sugar alcohols (polyols) such as D-mannitol, glycerol, D-sorbitol, and so on. Gluconobacter species also oxidize sugars and sugar acids and uniquely accumulate two different keto-D-gluconates
T Salusjärvi et al.
Applied microbiology and biotechnology, 65(3), 306-314 (2004-04-03)
A 5-ketogluconate (5-KGA)-forming membrane quinoprotein, gluconate dehydrogenase, was isolated from Gluconobacter suboxydans strain IFO 12528 and partially sequenced. Partial sequences of five internal tryptic peptides were elucidated by mass spectrometry and used to isolate the two adjacent genes encoding the
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
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