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A9524

Sigma-Aldrich

DL-Arabinose

≥98% (GC)

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C5H10O5
CAS-Nummer:
147-81-9
Molekulargewicht:
150.13
Beilstein:
1723086
EG-Nummer:
205-699-8
MDL-Nummer:
MFCD00135867
UNSPSC-Code:
12352201
PubChem Substanz-ID:
24891465
NACRES:
NA.25

Biologische Quelle

cell culture

Qualitätsniveau

100

Assay

≥98% (GC)

Form

powder

Methode(n)

gas chromatography (GC): suitable

Farbe

white to off-white

Löslichkeit

water: 50 mg/mL, clear, colorless

Lagertemp.

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

InChIKey

PYMYPHUHKUWMLA-VAYJURFESA-N

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Anwendung

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.

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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-
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
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
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
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