Skip to Content
Merck
CN
All Photos(1)

Key Documents

View All Documentation

Safety Information

68397

Sigma-Aldrich

Trehalose 6-octanoate

≥95.0% (GC)

Synonym(s):

α,α-Trehalose 6-caprylate, α-D-Glucopyranosyl-α-D-glucopyranoside 6-octanoate, Trehalose 6-caprylate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C20H36O12
CAS Number:
64622-90-8
Molecular Weight:
468.49
UNSPSC Code:
12161900
PubChem Substance ID:
329760885
NACRES:
NA.25

Assay

≥95.0% (GC)

form

powder

mol wt

468.49 g/mol

CMC

5.6 mM

storage temp.

2-8°C

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

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.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

监管及禁止进口产品

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBQ2451V
BCBQ5573V
BCBQ5573
BCBQ2451

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service