E7625
D-(−)-Erythrose
≥75% (TLC), syrup
Sinónimos:
(2R,3R)-2,3,4-trihydroxybutanal
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Fórmula empírica (notación de Hill):
C4H8O4
Número CAS:
Peso molecular:
120.10
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
209-505-2
Beilstein/REAXYS Number:
1721698
MDL number:
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Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥75% (TLC)
form
syrup
color
colorless to very dark yellow
storage temp.
2-8°C
SMILES string
[H]C(=O)[C@H](O)[C@H](O)CO
InChI
1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m0/s1
InChI key
YTBSYETUWUMLBZ-IUYQGCFVSA-N
Application
D-(-)-Erythrose, the D enantiomer of the aldose aldehyde erythrose, may be used as a reference compound in sugar metabolism analysis. D-(-)-Erythrose may be used to help identify and characterize erythrose reductase(s). D-Erythrose may be used to study the mechanisms of mutarotation in monosugars.[1] D-Erythrose may be used to study the mechanisms of organic microspherule formation and Maillard (glycation) reactions.[2]
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.
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Este artículo | |||
|---|---|---|---|
| assay ≥75% (TLC) | assay ≥97.0% (GC) | assay 99% | assay ≥98.5% (sum of enantiomers, GC), 99% |
| Quality Level 200 | Quality Level 100 | Quality Level 200 | Quality Level 100 |
| form syrup | form powder | form solid | form crystals |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. - | storage temp. - |
| color colorless to very dark yellow | color white to off-white | color - | color - |
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Dae-Hee Lee et al.
Microbial cell factories, 9, 43-43 (2010-06-10)
Erythrose reductase (ER) catalyzes the final step of erythritol production, which is reducing erythrose to erythritol using NAD(P)H as a cofactor. ER has gained interest because of its importance in the production of erythritol, which has extremely low digestibility and
Julia Schörghuber et al.
Journal of biomolecular NMR, 71(3), 129-140 (2018-05-29)
In recent years, we developed a toolbox of heavy isotope containing compounds, which serve as metabolic amino acid precursors in the E. coli-based overexpression of aromatic residue labeled proteins. Our labeling techniques show excellent results both in terms of selectivity
Arthur L Weber
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 35(6), 523-536 (2005-10-29)
Reaction of small sugars of less than four carbons with ammonia in water yielded organic microspherules generally less than ten microns in size. The time course of microspherule growth was examined for the D-erythrose-ammonia reaction that yielded microspherules attached to
Número de artículo de comercio global
| SKU | GTIN |
|---|---|
| E7625-1G | 04061826059241 |
| E7625-250MG | 04061833608425 |