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Merck

S2054

Sigma-Aldrich

Sodium gluconate

meets USP testing specifications

Sinónimos:

D-Gluconic acid sodium salt, 2,3,4,5,6-Pentahydroxycaproic acid sodium salt, D-Gluconate sodium salt, Sodium D-gluconate

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About This Item

Fórmula empírica (notación de Hill):
C6H11NaO7
Número de CAS:
Peso molecular:
218.14
Beilstein/REAXYS Number:
3919651
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.21

biological source

microbial

Quality Level

agency

USP/NF
meets USP testing specifications

form

solid

color

beige

useful pH range

6.5 - 7.5

mp

170-175  °C

solubility

590 g/L at 25 °C

application(s)

pharmaceutical (small molecule)

storage temp.

room temp

SMILES string

[Na+].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O

InChI

1S/C6H12O7.Na/c7-1-2(8)3(9)4(10)5(11)6(12)13;/h2-5,7-11H,1H2,(H,12,13);/q;+1/p-1/t2-,3-,4+,5-;/m1./s1

InChI key

UPMFZISCCZSDND-JJKGCWMISA-M

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Application

Sodium gluconate has been used as a component of recording buffer used in two-electrode voltage-clamp (TEVC) recording in Xenopus laevis oocytes. It has also been used as a control for sodium.

Biochem/physiol Actions

Ingestion of sodium gluconate is known to stimulate the production of intestinal butyrate. It is widely used in food, pharmaceutical paper and textile industry. It acts as a chelating agent. Sodium gluconate serves as a detergent in bottle washing formulation.

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Dietary sodium gluconate protects rats from large bowel cancer by stimulating butyrate production
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Wang C, et al.
Bio-protocol, 7(2) (2017)
Gluconic acid: Properties, applications and microbial production.
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