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O6004

Octyl β-D-1-thioglucopyranoside

≥98.0% (GC)

Synonym(s):

Octyl thioglucoside

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About This Item

Empirical Formula (Hill Notation):
C14H28O5S
CAS Number:
85618-21-9
Molecular Weight:
308.43
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24898030
MDL number:
MFCD00012189
Beilstein/REAXYS Number:
4182783

Key Documents

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Product Name

Octyl β-D-1-thioglucopyranoside, ≥98.0% (GC)

InChI

1S/C14H28O5S/c1-2-3-4-5-6-7-8-20-14-13(18)12(17)11(16)10(9-15)19-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14+/m1/s1

SMILES string

CCCCCCCCS[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI key

CGVLVOOFCGWBCS-RGDJUOJXSA-N

biological source

synthetic

description

non-ionic

assay

≥98.0% (GC)

form

crystalline

optical activity

[α]25/D -51 to -49 °, c = 1% (w/v) in ethanol

mol wt

308.43 g/mol

CMC

9 mM (20-25°C)

storage temp.

−20°C

Quality Level

200

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1 of 4

This Item
O9882O8001H3264
Octyl β-D-1-thioglucopyranoside ≥98.0% (GC)

Sigma-Aldrich

O6004

Octyl β-D-1-thioglucopyranoside

Octyl β-D-glucopyranoside BioXtra, ≥98% (GC)

Sigma-Aldrich

O9882

Octyl β-D-glucopyranoside

Octyl β-D-glucopyranoside ≥98% (GC)

Sigma-Aldrich

O8001

Octyl β-D-glucopyranoside

n-Heptyl β-D-thioglucopyranoside ≥99% (GC)

Sigma-Aldrich

H3264

n-Heptyl β-D-thioglucopyranoside

assay

≥98.0% (GC)

assay

≥98% (GC)

assay

≥98% (GC)

assay

≥99% (GC)

biological source

synthetic

biological source

-

biological source

-

biological source

-

Quality Level

200

Quality Level

200

Quality Level

300

Quality Level

100

form

crystalline

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

description

non-ionic

description

non-ionic

description

non-ionic

description

non-ionic

Application

Octyl β-D-1-thioglucopyranoside can be used as a non-ionic detergent for solubilization and reconstitution of membrane proteins. It has been used in a study to assess the crystallization and preliminary x-ray analysis of human plasma apolipoprotein C-I. [1] It has also been used in a study that investigated the identification of Chlamydia pneumoniae proteins. [2]

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000502844
0000502844
0000479130
0000479130
0000491542

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M Yoshida et al.
European journal of biochemistry, 222(3), 1055-1061 (1994-06-15)
Dystrophin is purified as a complex with several proteins from the digitonin-solubilized muscle cell membrane. Most of dystrophin-associated proteins (DAPs) are assumed to form a large oligomeric transmembranous glycoprotein complex on the sarcolemma and link dystrophin with a basement membrane
K H Weisgraber et al.
Journal of molecular biology, 236(1), 382-384 (1994-02-11)
Human apolipoprotein C-I, the smallest of the plasma apolipoproteins, is a component of several classes of plasma lipoproteins. Two crystalline forms of this protein, both suitable for high resolution X-ray diffraction analysis, have been obtained from mixtures of 2-methyl-2,4-pentanediol, sodium
Sanghamitra Mukhopadhyay et al.
Molecular & cellular proteomics : MCP, 5(12), 2311-2318 (2006-08-22)
Chlamydia pneumoniae is an important human respiratory pathogen that is responsible for an estimated 10% of community-acquired pneumonia and 5% of bronchitis and sinusitis cases. We examined changes in global protein expression profiles associated with the redifferentiation of reticulate body
M Chami et al.
Journal of structural biology, 133(1), 64-74 (2001-05-18)
A great interest exists in producing and/or improving two-dimensional (2D) crystals of membrane proteins amenable to structural analysis by electron crystallography. Here we report on the use of the detergent n-octyl beta-d-thioglucopyranoside in 2D crystallization trials of membrane proteins with
K Suzuki et al.
The Journal of pharmacology and experimental therapeutics, 288(1), 57-64 (1998-12-23)
A specific sugar-modified peptide has previously been shown to have renal targeting potential in vivo and to have a specific binding site which has been identified in the kidney membrane fraction. In this report, we studied the inhibitory effects of
View All Related Papers

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