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85541

L-(−)-Sorbose

Name: <SC>L-</SC>(−)-Sorbose
Brand: SIGMA

for biotechnological purposes, ≥98.0% (sum of enantiomers, HPLC)

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Fórmula empírica (notación de Hill):

C₆H₁₂O₆

Número CAS:

87-79-6

Peso molecular:

180.16

UNSPSC Code:

12352201

NACRES:

NA.25

PubChem Substance ID:

57653051

EC Number:

201-771-8

Beilstein/REAXYS Number:

1724554

MDL number:

MFCD00151097

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Quality Level

200

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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Este artículo	63582	63580	63579
Sigma-Aldrich 85541 L-(−)-Sorbose	Millipore 63582 D-(+)-Mannose	Millipore 63580 D-(+)-Mannose	Sigma-Aldrich 63579 D-(+)-Mannose
assay ≥98.0% (sum of enantiomers, HPLC)	assay ≥99.0% (sum of enantiomers, HPLC)	assay ≥99%, ≥99.0% (sum of enantiomers, HPLC)	assay ≥99.5% (sum of enantiomers, HPLC)
solubility H₂O: 0.1 g/mL, clear, colorless to very faintly yellow	solubility H₂O: 0.1 g/mL, clear, colorless	solubility H₂O: 0.1 g/mL, clear, colorless	solubility H₂O: 1 M, clear, colorless
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
form solid	form powder	form powder	form solid
mp 163-165 °C	mp 133-140 °C (lit.)	mp 133-140 °C (lit.)	mp 133-140 °C (lit.)
color colorless	color -	color -	color white

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.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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High-Throughput Screening of a 2-Keto-L-Gulonic Acid-Producing Gluconobacter oxydans Strain Based on Related Dehydrogenases.

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

Production of 2-keto-L-gulonic acid by metabolically engineered Escherichia coli.

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

Biochemical and mutational analyses of a Trametes pyranose oxidase and comparison of its mutants in breadmaking.

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

Selective carbon sources influence the end products of microbial nitrate respiration.

Hans K Carlson et al.

The ISME journal, 14(8), 2034-2045 (2020-05-07)

Respiratory and catabolic genes are differentially distributed across microbial genomes. Thus, specific carbon sources may favor different respiratory processes. We profiled the influence of 94 carbon sources on the end products of nitrate respiration in microbial enrichment cultures from diverse

Reconstruction of amino acid biosynthetic pathways increases the productivity of 2-keto-L-gulonic acid in Ketogulonicigenium vulgare-Bacillus endophyticus consortium via genes screening.

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

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Número de artículo de comercio global

SKU	GTIN
700959-25G	04061832595870
700959-5G	04061832595887
85541-250G	04061833025031
85541-50G	04061833025086

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