DEXTROSE

DEXTROSE Basic information
Product Name:DEXTROSE
Synonyms:DEXTROSUM;D-GLC;D-(+)-DEXTROSE;GLUCOSE STANDARD;GLUCOSUM;GRAPE SUGAR;ALPHA-D(+)-GLUCOSE;ALPHA-D-GLUCOSE
CAS:492-62-6
MF:C6H12O6
MW:180.16
EINECS:207-757-8
Product Categories:Food additive and sweetener;Biochemicals and Reagents;BioUltraBiochemicals and Reagents;BioUltraMolecular Biology;Carbohydrates;Molecular Biology Reagents;Monosaccharide
Mol File:492-62-6.mol
DEXTROSE Structure
DEXTROSE Chemical Properties
Melting point 153-156 °C(lit.)
Boiling point 232.96°C (rough estimate)
density 1.544g/cm3
refractive index n20/D 1.362
storage temp. Sealed in dry,Room Temperature
solubility H2O: 1 M at 20 °C, clear, colorless
pka12.12±0.70(Predicted)
form solution
color White
PH5.0-8.0 (25℃)
Odorodorless
optical activity[α]20/D +52°, c = 10 in H2O
Water Solubility 450.5g/L(25 ºC)
λmaxλ: 260 nm Amax: 0.04
λ: 280 nm Amax: 0.04
BRN 1281608
LogP-1.880 (est)
CAS DataBase Reference492-62-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany 3
RTECS LZ6600000
3
HS Code 17023000
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
DEXTROSE Usage And Synthesis
Chemical Propertieswhite, odorless, fine crystalline powder
Usesα-D-Glucose is used:
  • As a reducing agent in the preparation superparamagnetic ferrous oxide (Fe3O4) nanoparticles and silver nanocrystals.
  • As an additive for the formation of isoporous polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) diblock copolymer membranes.
  • For glycosylation of cell-penetrating poly(disulfide)s (CPDs) with improved solubility to achieve multifunctional cellular uptake.
  • As a precursor in the synthesis of metal/carbon nanohybrids under hydrothermal conditions.

UsesD-(+)-Glucose is a common natural sugar involved in processes such as energy production, glycosylation, and formation of glycans that provide structure to cells. Glucose is involved in a detrimentatl process in cells called glycation. Glucose is used as a supplement for cell culture and in numerous cellular processes and molecular biology applications.
DefinitionChEBI: D-Glucopyranose having alpha-configuration at the anomeric centre.
Purification MethodsRecrystallise -D-glucose slowly from aqueous 80% EtOH, then dry it over P2O5 in vacuo. Alternatively, crystallise it from water at 55o, then dry it for 6hours in a vacuum oven between 60-70o/2mm. Its solubilities are: H2O (~50%), EtOH (1.7%). [Hendricks et al. J Am Chem Soc 56 99 1934, Beilstein 1 IV 4302.] [For equilibrium forms see Angyal Adv Carbohydr Chem 42 15 1984, Angyal & Pickles Aust J Chem 25 1711 1972.]
ALPHA-D-CELLOBIOSE OCTAACETATE Phlorizin METHYL BETA-D-GLUCOPYRANOSIDE D-(+)-MELEZITOSE ROBISON ESTER MONOSODIUM SALT MALTOTETRAOSE O-ALPHA-D-GLUCOPYRANOSYL-(1->4)-O-ALPHA-D-GLUCOPYRANOSYL-(1->4)-O-ALPHA-D-GLUCOSE 1,2,3,4,6-Penta-O-acetyl-b-D-glucopyranose D-Lactose monohy D-(+)-TURANOSE ALPHA-D-GLUCOSE-PENTABENZOATE 4,6-O-ETHYLIDENE-ALPHA-D-GLUCOSE 96+% 3-O-METHYL-D-GLUCOPYRANOSE Amygdalin STACHYOSE Maltitol 4-NITROPHENYL-BETA-D-GLUCOPYRANOSIDE Cyclooctapentylose

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