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Key Documents

A9524

Sigma-Aldrich

DL-Arabinose

≥98% (GC)

Synonym(s):

(2R,3R,4R)-2,3,4,5-tetrahydroxypentanal

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About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
Beilstein:
1723086
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

biological source

cell culture

Assay

≥98% (GC)

form

powder

technique(s)

gas chromatography (GC): suitable

color

white to off-white

solubility

water: 50 mg/mL, clear, colorless

storage temp.

room temp

SMILES string

OC[C@H](O)[C@H](O)[C@@H](O)C=O

InChI

1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1

InChI key

PYMYPHUHKUWMLA-VAYJURFESA-N

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Application

DL-Arabinose is a mixture of the diastereomers D-arabinose and L-arabinose used in physicochemical studies to measure properties such as dielectric relaxation. It may be used in chiral separation of sugars.

Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Karen L Visick et al.
Applied and environmental microbiology, 79(6), 2069-2080 (2013-01-22)
Biofilms are multicellular communities of bacteria attached to a surface and embedded in a protective matrix. In many cases, the signals that induce biofilm formation are unknown. Here, we report that biofilm formation by the marine bacterium Vibrio fischeri can
Silvia Herold et al.
Eukaryotic cell, 12(3), 390-398 (2013-01-08)
The ascomycete Trichoderma reesei is a paradigm for the regulation and production of plant cell wall-degrading enzymes, including xylanases. Four xylanases, including XYN1 and XYN2 of glycosyl hydrolase family 11 (GH11), the GH10 XYN3, and the GH30 XYN4, were already
Kamil Kaminski et al.
Carbohydrate research, 344(18), 2547-2553 (2009-10-28)
Dielectric relaxation measurements were performed on two enantiomers, D- and L-arabinose and their equimolar mixture, and compared to dielectric data obtained for D-ribose. D-Arabinose differs from d-ribose by having the opposite configuration at C2. This study reveals that both D-
Matthew B Kraft et al.
The Journal of organic chemistry, 78(5), 2128-2133 (2013-02-05)
Mycobacteria and corynebacteria use decaprenylphosphoryl-β-D-arabinofuranose (DPA) as a critical cell wall building block. Arabinofuranosyltransferases that process this substrate to mediate cell wall assembly have served as drug targets, but little is known about the substrate specificity of any of these
Anna N Kondakova et al.
Journal of natural products, 75(12), 2236-2240 (2012-12-01)
A novel constituent of bacterial polysaccharides, 2,3,4-triacetamido-2,3,4-trideoxy-L-arabinose, was found in the O-specific polysaccharide from the lipopolysaccharide of Psychrobacter cryohalolentis K5(T) and identified by 1D and 2D (1)H and (13)C NMR studies of the polysaccharide and a disaccharide obtained by solvolysis

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