Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

30679

Sigma-Aldrich

Trehalose 6-decanoate

≥95.0% (GC)

Synonym(s):

α,α-Trehalose 6-caprate, α-D-Glucopyranosyl-α-D-glucopyranoside 6-decanoate, Trehalose 6-caprate

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

About This Item

Empirical Formula (Hill Notation):
C22H40O12
CAS Number:
924885-56-3
Molecular Weight:
496.55
UNSPSC Code:
12161900
PubChem Substance ID:
329753561
NACRES:
NA.25

Assay

≥95.0% (GC)

form

powder

mol wt

496.55 g/mol

technique(s)

protein quantification: suitable

CMC

3 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(CCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O

InChI

1S/C22H40O12/c1-2-3-4-5-6-7-8-9-14(24)31-11-13-16(26)18(28)20(30)22(33-13)34-21-19(29)17(27)15(25)12(10-23)32-21/h12-13,15-23,25-30H,2-11H2,1H3/t12?,13?,15-,16-,17?,18?,19+,20+,21-,22-/m1/s1

InChI key

NWUMPUQFMKERLR-FLRCUGBKSA-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

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCC7761
BCBZ9005
BCBR6783V
BCBQ2452V
BCBQ2452

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

L Schiefelbein et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 76(3), 342-350 (2010-09-08)
Nonionic polyethylene glycol-derived surfactants are today's choice as surfactants in protein formulations. Different groups discovered that although surface-induced stresses are reduced by these excipients, the long-term stability of different proteins decreased due to polyethylene glycol-related induction of oxidation processes under
Surface activities of monoacyl trehaloses in aqueous solution.
Chen, J., et al.
Food Sci. Technol., 40, 412-417 (2006)

Questions

Reviews

No rating value

Active Filters

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