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Merck
CN

A9524

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
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
205-699-8
Beilstein/REAXYS Number:
1723086
MDL number:
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biological source

cell culture

Quality Level

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

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

涉药品监管产品

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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
Akiyoshi Ikeda-Boku et al.
Journal of biochemistry, 153(3), 317-326 (2013-01-15)
We developed an efficient method for introduction of 3-azidotyrosine (N(3)-Y) into proteins in Escherichia coli cells. We constructed a plasmid that is adaptable for the constitutive expression of both Methanosarcina acetivorans tyrosyl-tRNA synthetase (TyrRS) and tRNA(()(CUA)), and made an orthogonal



Global Trade Item Number

SKUGTIN
A9524-5G04061832387161
A9524-10G04061833402825
A9524-50G04061833402863