85541
L-(−)-Sorbose
for biotechnological purposes, ≥98.0% (sum of enantiomers, HPLC)
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经验公式（希尔记法）:
C6H12O6
化学文摘社编号:
分子量:
180.16
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
201-771-8
Beilstein/REAXYS Number:
1724554
MDL number:
产品名称
L-(−)-Sorbose, for biotechnological purposes, ≥98.0% (sum of enantiomers, HPLC)
InChI key
BJHIKXHVCXFQLS-OTWZMJIISA-N
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
SMILES string
OC[C@H](O)[C@@H](O)[C@H](O)C(=O)CO
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
Quality Level
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
涉药品监管产品
此项目有
Praveen Kumar Reddy et al.
Yeast (Chichester, England), 38(3), 222-238 (2020-11-13)
Human fungal pathogen Candida albicans cannot utilize L-sorbose as a sole carbon source. However, chromosome 5 monosomic strains can grow on sorbose as repressors present on this chromosome get diminished allowing the expression of sorbose utilization gene (SOU1) located on
Raquel Barajas-Azpeleta et al.
PLoS genetics, 14(10), e1007440-e1007440 (2018-10-13)
Antimicrobial peptides act as a host defense mechanism and regulate the commensal microbiome. To obtain a comprehensive view of genes contributing to long-term memory we performed mRNA sequencing from single Drosophila heads following behavioral training that produces long-lasting memory. Surprisingly
Xiaoyu Shan et al.
Frontiers in bioengineering and biotechnology, 8, 194-194 (2020-04-08)
2-Keto-L-gulonic acid (2-KLG) is the direct precursor for the production of L-ascorbic acid (L-Asc) on industrial scale. Currently, the production of L-Asc in the industry is a two-step fermentation process. Owing to many unstable factors in the fermentation process, the
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
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
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