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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:
147-81-9
Molecular Weight:
150.13
Beilstein:
1723086
EC Number:
205-699-8
MDL number:
MFCD00135867
UNSPSC Code:
12352201
PubChem Substance ID:
24891465
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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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
Mei Jiang et al.
Journal of natural products, 76(4), 764-768 (2013-03-13)
Three new 19-hydroxy steroidal glycosides, namely, junceellosides E-G (2-4), were isolated together with the known analogue junceelloside C (1) from the South China Sea gorgonian Dichotella gemmacea. The structures of these compounds were elucidated by a combination of detailed spectroscopic
Susanna L Heikkinen et al.
Carbohydrate polymers, 92(1), 733-740 (2012-12-12)
To increase understanding of the applicability of agro biomass by-products as biodegradable film formers, the effect of wheat arabinoxylan (WAX) fine structure on film properties was studied by applying specific enzyme modifications. WAX was selectively modified to mimic the natural
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
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