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Merck
CN

68397

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C20H36O12
CAS号:
分子量:
468.49
UNSPSC代码:
12161900
PubChem化学物质编号:
NACRES:
NA.25

方案

≥95.0% (GC)

表单

powder

分子量

468.49 g/mol

CMC

5.6 mM

储存温度

2-8°C

SMILES字符串

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

应用

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.

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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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