Biovalley > L-Sorbose [87-79-6]
L-Sorbose [87-79-6]
Référence MS05200-25g
Conditionnement : 25g
Marque : Biosynth
CAS No
[87-79-6]
Synonyms
(3S,4R,5S)-1,3,4,5,6-Pentahydroxyhexan-2-one
Product Code
MS05200
MDL No
MFCD00151097
MOL file
Chemical Formula
C6H12O6
Molecular Weight
180.16 g/mol
Smiles
C([C@@H]([C@H]([C@@H](C(=O)CO)O)O)O)O
Melting Point
164 °C
Long Term Storage
store at 10°C - 25°C, keep under inert gas: Nitrogen, protect from light
Storage
store at 10°C - 25°C, keep under inert gas: Nitrogen, protect from light
Precautionary Statement Code
P261, P262
Harmonized Tariff Codes
Switzerland: 29400000 - USA: 2914409000 - Slovakia: 2940000080 - UK: 2940000000 - China: 2940009000
Resource for the industrial synthesis of ascorbic acid alias Vitamin C
- Reichstein et al (1933). Eine ergiebige Synthese der lâAscorbinsÃ(1): 311-328.
- Itoh and Izumori (1996). Enzymatic production of l-tagatose and l-fructose from l-sorbose and l-psicose, respectively. Journal of Fermentation and Bioengineering, 81(4): 351-353.
- Sahoo et al (1986). Influence of L-Sorbose on Growth and Enzyme Synthesis of Trichoderma reesei C-5. Journal of General Microbiology, 132:2761-2766.
- Leang et al (2004). A novel enzymatic approach to the massproduction of L-galactose from L-sorbose. Journal of Bioscience and Bioengineering, 97(6): 383-388.
- Ogawa et al (1983). Microbial Production of Optically Pure L-Iditol by Yeast Strains. Applied and Environmental Microbiology, 46(4):912-916.
- Perlin and Brice (1956). Reaction of aldoses and ketoses with lead tetraacetate. Canadian Journal of Chemistry, 34(4):541-553.

