E7625
D-(−)-Erythrose
≥75% (TLC), syrup
Synonyme(s) :
(2R,3R)-2,3,4-trihydroxybutanal
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| Conditionnement | Référence | Disponibilité | Prix |
|---|
A propos de cet article
Formule empirique (notation de Hill) :
C4H8O4
Numéro CAS:
Poids moléculaire :
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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Laissez-nous vous aiderQuality 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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Cet article | |||
|---|---|---|---|
| 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 - |
Classe de stockage
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
Danielle Rand et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 41(1), 17-22 (2010-06-22)
Reactions of short sugars under mild, plausibly prebiotic conditions yield organic microspherules that may have played a role in prebiotic chemistry as primitive reaction vessels. It has been widely thought that nitrogen chemistry, in particular Amadori rearrangement, is central to
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| E7625-250MG | 04061833608425 |
| E7625-1G | 04061826059241 |