D-(-)-Arabinose, 99%
D-(-)-Arabinose, 99%
D-(-)-Arabinose, 99%
D-(-)-Arabinose, 99%
Thermo Scientific Chemicals

D-(-)-Arabinose, 99%

CAS: 10323-20-3 | C5H10O5 | 150.13 g/mol
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Catalog NumberQuantity
ALFA10357.1850 g
Catalog number ALFA10357.18
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Quantity:
50 g
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Chemical Identifiers
CAS1310-66-3
IUPAC Namelithium(1+) hydrate hydroxide
Molecular FormulaH3LiO2
InChI KeyGLXDVVHUTZTUQK-UHFFFAOYSA-M
SMILES[Li+].O.[OH-]
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SpecificationsSpecification SheetSpecification Sheet
Chloride content≤500ppm (≤0.05%)
Impurity contentCO2: ≤3500ppm (≤0.35%)
Impurity contentIron, Fe: ≤10ppm (≤0.001%)
Impurity contentSulphate, SO4: ≤500ppm (≤0.005%)
Insoluble material≤0.1% (in water)
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D-(-)-Arabinose is used in culture media for some bacteria. It serves as a component of biopolymers such as hemicellulose and pectin. In the synthetic biology laboratory, it is employed as a reversible switch for protein expression under the Pbad promoter (i.e. part of plasmids) in E. coli. Further, it acts as an inhibitor of the enzyme glucose dehydrogenase. In addition to this, it is used as a pharmaceutical intermediate and food additive.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
D-(-)-Arabinose is used in culture media for some bacteria. It serves as a component of biopolymers such as hemicellulose and pectin. In the synthetic biology laboratory, it is employed as a reversible switch for protein expression under the Pbad promoter (i.e. part of plasmids) in E. coli. Further, it acts as an inhibitor of the enzyme glucose dehydrogenase. In addition to this, it is used as a pharmaceutical intermediate and food additive.

Solubility
Soluble in water.

Notes
Hygroscopic. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Chiral building block. For use in the synthesis of a chiral quinuclidine-3,5-diol, see: J. Chem. Soc., Perkin 1, 1065 (1989).
  2. van Putten, R. J.; Winkelman, J. G.; Keihan, F.; van der Waal, J. C.; de Jong, E.; Heeres, H. J. Experimental and Modeling Studies on the Solubility of d-Arabinose, d-Fructose, d-Glucose, d-Mannose, Sucrose and d-Xylose in Methanol and Methanol-Water Mixtures. Ind. Eng. Chem. Res. 2014, 53 (19), 8285-8290.
  3. Singh, V.; Banipal, P. K.; Banipal, T. S.; Gardas, R. L. Volumetric properties of 1-butyl-3-methylimidazolium bromide in aqueous solutions of d(-)-ribose and d(-)-arabinose at different temperatures. J. Mol. Liq. 2015, 209, 352-357.