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G9130

Sigma-Aldrich

Magnesium D-gluconate hydrate

≥98% (HPLC)

Sinónimos:

D-Gluconic acid hemimagnesium salt, D-Gluconic acid magnesium salt

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About This Item

Fórmula empírica (notación de Hill):
C12H22MgO14 · xH2O
Número de CAS:
3632-91-5
Peso molecular:
414.60 (anhydrous basis)
EC Number:
222-848-2
MDL number:
MFCD00150971
UNSPSC Code:
12352201
PubChem Substance ID:
24895362
NACRES:
NA.25

assay

≥98% (HPLC)

form

powder

technique(s)

HPLC: suitable

SMILES string

O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(=O)O[Mg]OC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

InChI

1S/2C6H12O7.Mg.H2O/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;;/h2*2-5,7-11H,1H2,(H,12,13);;1H2/q;;+2;/p-2/t2*2-,3-,4+,5-;;/m11../s1

InChI key

IAKLPCRFBAZVRW-XRDLMGPZSA-L

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Biochem/physiol Actions

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. It is a strong chelating agent, chelating the anions of calcium, iron, aluminum, copper, and other heavy metals.

Other Notes

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100.00 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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Food chemistry, 134(2), 1005-1010 (2012-10-31)
The structural changes and aggregation properties of silver carp actomyosin acidified with d-gluconic acid-δ-lactone (GDL) were investigated. Results showed that silver carp actomyosin underwent aggregation and formation of precipitate as indicated by turbidity and centrifugation coupled electrophoresis analysis. Circular dichroism
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