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Merck
CN

G9005

D-Gluconic acid sodium salt

≥99% (HPLC)

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C6H11NaO7
CAS Number:
527-07-1
Molecular Weight:
218.14
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
57654222
EC Number:
208-407-7
Beilstein/REAXYS Number:
3919651
MDL number:
MFCD00064210

Key Documents

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Product Name

D-Gluconic acid sodium salt, ≥99% (HPLC)

InChI key

UPMFZISCCZSDND-JJKGCWMISA-M

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

SMILES string

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

biological source

microbial

assay

≥99% (HPLC)

form

powder or crystals

technique(s)

HPLC: suitable

color

white to off-white

useful pH range

6.5-7.5

mp

170-175  °C

solubility

590 g/L at 25 °C

application(s)

agriculture

storage temp.

room temp

Quality Level

200

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Application

D-Gluconic acid sodium salt has been used:
  • as a component to make synthetic interstitial fluid.
  • used as a carbohydrate.
  • used as a substitute for sodium chloride to make chlorine (Cl-) free media.

Biochem/physiol Actions

D-Gluconic acid is a mild organic acid with non-corrosive, non-odorous, non-volatile and biodegradable property. Enzymatic conversion of D-Glucose results in the final product D-Gluconic acid. Gluconic acid occurs from the oxidation of glucose and is naturally in fruit, honey and wine. When used as a food additive it helps regulate acidity. Sodium salt of D-gluconic acid is a strong chelating agent, chelating the anions of calcium, iron, aluminium, copper, and other heavy metals. It finds wide application in detergent industry for bottle washing, descaling of salt deposits and alkaline derusting. D-Gluconic acid usage as an additive in cement, gives strength and water resistance.

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

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF6947V
BCCN5854
WXBF5952V
BCCM8528
BCCM0342

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Serratia marcescens quinoprotein glucose dehydrogenase activity mediates medium acidification and inhibition of prodigiosin production by glucose.
Fender JE, et al.
Applied and Environmental Microbiology, AEM-01778 (2012)
Phenotyping sensory nerve endings in vitro in the mouse
Zimmermann K, et al.
Nature Protocols, 4(2), 174-196 (2009)
Gluconic acid: Properties, applications and microbial production.
Ramachandran S, et al.
Food Technology and Biotechnology, 44(2), 185-195 (2006)
Evaluation of intracellular pH regulation and alkalosis defense mechanisms in preimplantation embryos
Dagilgan S, et al.
Theriogenology, 83(6), 1075-1084 (2015)
Yasaman Barekatain et al.
Communications biology, 3(1), 328-328 (2020-06-27)
Magnetic resonance (MR) spectroscopy has potential to non-invasively detect metabolites of diagnostic significance for precision oncology. Yet, many metabolites have similar chemical shifts, yielding highly convoluted 1H spectra of intact biological material and limiting diagnostic utility. Here, we show that
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