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About This Item
Empirical Formula (Hill Notation):
C26H48O12
CAS Number:
Molecular Weight:
552.65
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25
Assay:
≥95.0% (GC)
Form:
powder
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(CCCCCCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI
1S/C26H48O12/c1-2-3-4-5-6-7-8-9-10-11-12-13-18(28)35-15-17-20(30)22(32)24(34)26(37-17)38-25-23(33)21(31)19(29)16(14-27)36-25/h16-17,19-27,29-34H,2-15H2,1H3/t16?,17?,19-,20-,21?,22?,23+,24+,25-,26-/m1/s1
InChI key
LRXBVTKVELRWDT-AULNSQLGSA-N
assay
≥95.0% (GC)
form
powder
CMC
0.012 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.
Other Notes
To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Displacer Chemistry on Displacer Efficacy for a Sugar-Based Anion Exchange Displacer Library.
Liu, J., et al.
Industrial & Engineering Chemistry Research, 45, 9107-9114 (2006)
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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