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E0758

Sigma-Aldrich

L(+)-Erythrose

~40%, syrup

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About This Item

Empirische Formel (Hill-System):
C4H8O4
CAS-Nummer:
533-49-3
Molekulargewicht:
120.10
Beilstein:
1721697
EG-Nummer:
208-567-8
MDL-Nummer:
MFCD00064377
UNSPSC-Code:
12352201
PubChem Substanz-ID:
24894372
NACRES:
NA.25

Form

syrup

Konzentration

~40%

Farbe

light yellow

Lagertemp.

2-8°C

SMILES String

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

InChI

1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m1/s1

InChIKey

YTBSYETUWUMLBZ-DMTCNVIQSA-N

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Anwendung

L(+)-Erythrose, an aldotetrose rare sugar, may be used in glycation studies and as a reference compound in tetrose carbohydrate separation and quantitation analysis. It may be used to help identify and characterize erythrose reductase(s) and to study the mechanisms of mutarotation in monosugars. L-Erythrose may be used as a reference compound in sugar metabolism analysis.

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

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves

Analysenzertifikate (COA)

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R M Mizanur et al.
Journal of bioscience and bioengineering, 92(3), 237-241 (2005-10-20)
A rare aldotetrose, L-erythrose, was produced from erythritol via a two-step reaction. In the first step, complete oxidation of erythritol to L-erythrulose was achieved by using Gluconobacter frateurii IFO 3254. Washed cell suspension of the strain grown on tryptic soy
Eun-Hee Park et al.
Journal of microbiology and biotechnology, 21(10), 1064-1068 (2011-10-28)
The osmotolerant yeast, Candida magnoliae, which was isolated from honeycomb, produces erythritol from sugars such as fructose, glucose, and sucrose. Erythrose reductase in C. magnoliae (CmER) reduces erythrose to erythritol with concomitant oxidation of NAD(P)H. Sequence analysis of the 5'-flanking
Luis Miguel Azofra et al.
Carbohydrate research, 372, 1-8 (2013-03-19)
The acid catalysis of the mutarotation mechanism in the two aldotetroses, d-erythrose and d-threose, has been studied at B3LYP/6-311++G(d,p) computational level in gas phase and in solution employing the PCM-water model. The open-chain, the furanose and the connecting TS structures
Katsushi Nishimura et al.
Journal of bioscience and bioengineering, 101(4), 303-308 (2006-05-24)
We have identified the enzyme responsible for erythritol utilization and its reaction product in the yeast Lipomyces starkeyi CBS 1807. The enzyme, a polyol dehydrogenase requiring NAD+ as a coenzyme, was induced by erythritol in this yeast. We confirmed that
Ludwika Tomaszewska et al.
Applied biochemistry and biotechnology, 172(6), 3069-3078 (2014-02-04)
The aim of this study was to examine the impact of divalent copper, iron, manganese, and zinc ions on the production of erythritol from glycerol by Yarrowia lipolytica and their effect on the activity of erythrose reductase. No inhibitory effect
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