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About This Item
Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
Molecular Weight:
180.16
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
201-771-8
Beilstein/REAXYS Number:
1724554
MDL number:
Quality Level
assay
≥98.0% (sum of enantiomers, HPLC)
form
solid
optical activity
[α]20/D −43±2°, c = 5% in H2O
color
colorless
mp
163-165 °C
solubility
H2O: 0.1 g/mL, clear, colorless to very faintly yellow
SMILES string
OC[C@H](O)[C@@H](O)[C@H](O)C(=O)CO
InChI
1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5+,6+/m0/s1
InChI key
BJHIKXHVCXFQLS-OTWZMJIISA-N
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Application
L-Sorbose is used as a starting reagent for the commercial biosynthesis of ascorbic acid (vitamin C).
Biochem/physiol Actions
The L enatiomer of sorbose, a ketohexose monosaccharide.
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
涉药品监管产品
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M Huang et al.
Journal of applied microbiology, 125(5), 1383-1395 (2018-07-28)
Oxidative stress limited the growth of cells and 2-keto-l-gulonic acid (2-KGA) production in vitamin C (Vc) fermentation system. The study aims to investigate the antioxidant effect of glutathione on promoting 2-KGA in Vc fermentation system using Ketogulonicigenium vulgare 25B-1 and
Mengzhu Li et al.
AMB Express, 8(1), 38-38 (2018-03-15)
Pyranose oxidase (POx) is a homotetrameric flavoprotein that catalyzes the oxidation of pyranose-configured sugars at position C-2 to corresponding 2-ketoaldoses. The wide substrate specificity makes POx potential for application in various biotechnological industries. In the present study we reported the
Yue Chen et al.
Frontiers in bioengineering and biotechnology, 7, 385-385 (2020-01-11)
High-throughput screening is a powerful tool for discovering strains in the natural environment that may be suitable for target production. Herein, a novel enzyme-based high-throughput screening method was developed for rapid screening of strains overproducing 2-keto-L-gulonic acid (2-KLG). The screening
Weizhu Zeng et al.
Bioresource technology, 318, 124069-124069 (2020-09-12)
The 2-keto-L-gulonic acid (2-KLG) is the direct precursor for industrial vitamin C production. The main biosynthetic method for 2-KLG production is the classical two-step fermentation route. However, disadvantages of this method are emerging, including high consumption of energy, difficulties in
Cai-Hui Pan et al.
Journal of industrial microbiology & biotechnology, 44(7), 1031-1040 (2017-03-12)
Defect in the amino acid biosynthetic pathways of Ketogulonicigenium vulgare, the producing strain for 2-keto-L-gulonic acid (2-KGA), is the key reason for its poor growth and low productivity. In this study, five different strains were firstly reconstructed by expressing absent
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 700959-25G | 04061832595870 |
| 700959-5G | 04061832595887 |
| 85541-50G | 04061833025086 |
| 85541-250G | 04061833025031 |
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