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

D-(-)-Arabinose, 99%

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50 g
10 g
250 g
Catalog number A10357.18
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94.65
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Quantity:
50 g
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Price (USD)/ Each
94.65
Online exclusive
105.00 
Save 10.35 (10%)
Add to cart
D-(-)-Arabinose, 99%
Catalog numberA10357.18
Price (USD)/ Each
94.65
Online exclusive
105.00 
Save 10.35 (10%)
-
Add to cart
Chemical Identifiers
CAS10323-20-3
IUPAC Nameoxane-2,3,4,5-tetrol
Molecular FormulaC5H10O5
InChI KeySRBFZHDQGSBBOR-UHFFFAOYNA-N
SMILESOC1COC(O)C(O)C1O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream
FormPowder
Assay (Silylated GC)≥98.5%
Identification (FTIR)Conforms
Melting Point (clear melt)152.0-161.0?C
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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.