Record Information
Version1.0
Creation Date2016-05-19 02:12:46 UTC
Update Date2016-11-09 01:09:43 UTC
Accession NumberCHEM006355
Identification
Common NameMAGNESIUM GLUCONATE
ClassSmall Molecule
DescriptionMagnesium gluconate is a compound with formula MgC12H22O14. It is the magnesium salt of gluconic acid. According to one study, magnesium gluconate showed the highest level of bioavailability of any magnesium salt which implies its viability as a supplement, although of the 10 salts studied, all increased Magnesium levels significantly.It has E number "E580".
Contaminant Sources
  • EAFUS Chemicals
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Magnesium gluconic acidGenerator
Gluconic acid, sodium saltMeSH
Gluconic acid, potassium saltMeSH
Gluconic acid, zinc saltMeSH
Gluconic acid, cesium(+3) saltMeSH
Gluconic acid, magnesium (2:1) saltMeSH
Maltonic acidMeSH
Zinc gluconateMeSH
Gluconic acid, manganese (2:1) saltMeSH
GluconateMeSH
Gluconic acid, strontium (2:1) saltMeSH
D-Gluconic acidMeSH
Gluconic acid, (99)technecium (5+) saltMeSH
Gluconic acid, calcium saltMeSH
Gluconic acid, monolithium saltMeSH
Gluconic acid, (113)indium-labeledMeSH
Dextronic acidMeSH
Gluconic acid, (14)C-labeledMeSH
Boron gluconateMeSH
MagnerotMeSH
D-GluconateMeSH
Gluconic acid, copper saltMeSH
Gluconic acid, 1-(14)C-labeledMeSH
Gluconic acid, 6-(14)C-labeledMeSH
Lithium gluconateMeSH
Gluconic acid, cobalt (2:1) saltMeSH
Gluconic acid, tin(+2) saltMeSH
Gluconic acid, ammonium saltMeSH
Gluconic acid, (159)dysprosium-labeled saltMeSH
Gluconic acid, fe(+2) salt, dihydrateMeSH
Pentahydroxycaproic acidMeSH
Gluconic acid, aluminum (3:1) saltMeSH
Manganese gluconateMeSH
Gluconic acid, monopotassium saltMeSH
Gluconic acid, lanthanum(+3) saltMeSH
Sodium gluconateMeSH
Gluconic acidMeSH
Gluconic acid, monosodium saltMeSH
AlmoraChEMBL
Magnesium;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acidGenerator
Magnesium gluconateMeSH
Magnesium(2+) ion bis((2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid)Generator
Chemical FormulaC12H22MgO14
Average Molecular Mass414.599 g/mol
Monoisotopic Mass414.086 g/mol
CAS Registry Number3632-91-5
IUPAC Namemagnesium(2+) ion bis((2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate)
Traditional Namemagnesium(2+) ion bis(D-gluconate)
SMILES[Mg++].[H][C@@](O)(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]([H])(O)C([O-])=O.[H][C@@](O)(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]([H])(O)C([O-])=O
InChI IdentifierInChI=1S/2C6H12O7.Mg/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;/h2*2-5,7-11H,1H2,(H,12,13);/q;;+2/p-2/t2*2-,3-,4+,5-;/m11./s1
InChI KeyCTUVIUYTHWPELF-IYEMJOQQSA-L
Chemical Taxonomy
Description belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentSugar acids and derivatives
Alternative Parents
Substituents
  • Gluconic_acid
  • Medium-chain hydroxy acid
  • Medium-chain fatty acid
  • Beta-hydroxy acid
  • Hydroxy fatty acid
  • Hydroxy acid
  • Fatty acyl
  • Fatty acid
  • Monosaccharide
  • Secondary alcohol
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Polyol
  • Organic salt
  • Hydrocarbon derivative
  • Alcohol
  • Organic zwitterion
  • Organic oxide
  • Primary alcohol
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkNot Available
External DescriptorsNot Available
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility43.2 g/LALOGPS
logP-2ALOGPS
logP-3.4ChemAxon
logS-0.98ALOGPS
pKa (Strongest Acidic)3.39ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area141.28 ŲChemAxon
Rotatable Bond Count10ChemAxon
Refractivity49.11 m³·mol⁻¹ChemAxon
Polarizability16.62 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
SpectraNot Available
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDNot Available
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkMagnesium gluconate
Chemspider IDNot Available
ChEBI IDNot Available
PubChem Compound ID11418570
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available