68397
Trehalose 6-octanoate
≥95.0% (GC)
别名:
α,α-Trehalose 6-caprylate, α-D-Glucopyranosyl-α-D-glucopyranoside 6-octanoate, Trehalose 6-caprylate
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关于此项目
经验公式（希尔记法）:
C20H36O12
化学文摘社编号:
分子量:
468.49
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25
SMILES string
O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@H]2O[C@H](COC(CCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI
1S/C20H36O12/c1-2-3-4-5-6-7-12(22)29-9-11-14(24)16(26)18(28)20(31-11)32-19-17(27)15(25)13(23)10(8-21)30-19/h10-11,13-21,23-28H,2-9H2,1H3/t10?,11?,13-,14-,15?,16?,17+,18+,19-,20-/m1/s1
InChI key
WNPJPTWSRIRPIJ-LPKQXWMESA-N
assay
≥95.0% (GC)
form
powder
mol wt
468.49 g/mol
CMC
5.6 mM
storage temp.
2-8°C
Application
Trehalose is commonly used as a stabilizer and protective material for biomaterial compounds. Because of these characteristics, Trehalose is introduced as a hydrophilic part. Due to these properties of Trehalose, protein degeneration is expected to be prevented with Trehalose detergents. Therefore, Trehalose detergents may keep the function of the protein and be utilized in the field of proteomics research.
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
涉药品监管产品
此项目有
Hadar Feinberg et al.
The Journal of biological chemistry, 288(40), 28457-28465 (2013-08-21)
Binding of the macrophage lectin mincle to trehalose dimycolate, a key glycolipid virulence factor on the surface of Mycobacterium tuberculosis and Mycobacterium bovis, initiates responses that can lead both to toxicity and to protection of these pathogens from destruction. Crystallographic
Chemical and biochemical studies on carbohydrate esters. V. Anti Ehrlich ascites tumor effect and chromatographic behaviors of fatty acyl monoesters of sucrose and trehalose.
Y Nishikawa et al.
Chemical & pharmaceutical bulletin, 25(7), 1717-1724 (1977-07-01)
Surface activities of monoacyl trehaloses in aqueous solution.
Chen, J., et al.
Food Sci. Technol., 40, 412-417 (2006)
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