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O3757

Octyl β-D-glucopyranoside solution

≥95% (HPLC), 50 % (w/v) in H2O

Synonym(s):

n-Octyl glucoside, OGP

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About This Item

Empirical Formula (Hill Notation):
C14H28O6
CAS Number:
Molecular Weight:
292.37
NACRES:
NB.22
PubChem Substance ID:
UNSPSC Code:
12161902
MDL number:
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description

non-ionic

Quality Level

assay

≥95% (HPLC)

mol wt

average mol wt 24500-25000

concentration

50 % (w/v) in H2O

aggregation number

84

CMC

20-25

transition temp

cloud point ≥100

application(s)

detection

storage temp.

−20°C

SMILES string

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

InChI

1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1

InChI key

HEGSGKPQLMEBJL-RKQHYHRCSA-N

Application

2.5% n-octyl β-D glucopyranoside has been used to homogenize mouse retina
n-Octyl β-D-glucopyranoside (OGP) is a non-ionic detergent which has been used for isoelectric focusing (IEF) and two-dimensional electrophoresis (2D).[1] OGP has been shown to be superior to Triton X-100 for IEF of plant proteins. n-Octyl β-D-glucopyranoside has also been used for concentration of protein from 2D gels for digestion and mass spectroscopy analysis.[2]

Legal Information

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

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This Item
494459850511P10634425001
assay

≥95% (HPLC)

assay

≥98% (HPLC)

assay

>99% (contains <0.2% alpha isomer, TLC)

assay

99% (GC)

aggregation number

84

aggregation number

84

aggregation number

-

aggregation number

84

application(s)

detection

application(s)

-

application(s)

-

application(s)

-

storage temp.

−20°C

storage temp.

15-25°C

storage temp.

−20°C

storage temp.

-

description

non-ionic

description

-

description

n-octyl-β-D-glucopyranoside

description

-

CMC

20-25

CMC

20 - 25 mM

CMC

-

CMC

20-25 mM (20-25°C)


Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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P Dainese Hatt et al.
European journal of biochemistry, 246(2), 336-343 (1997-06-01)
We have developed a gel electrophoresis system that can concentrate proteins from spots cut out of up to 50 two-dimensional electrophoresis gels. During protein concentration, SDS is substituted with a non-ionic detergent (octyl beta-glucopyranoside) which allows digestion and MS analysis
Compartment-specific phosphorylation of phosducin in rods underlies adaptation to various levels of illumination.
Song H, et al.
The Journal of Biological Chemistry (2007)
M F Lopez
Journal of chromatography. B, Biomedical sciences and applications, 722(1-2), 191-202 (1999-03-06)
Two-dimensional electrophoresis has rapidly become the method of choice for resolving complex mixtures of proteins. Since the technique was pioneered in 1975, 2-D gel methods have undergone a series of enhancements to optimize resolution and reproducibility. Recent improvements in the



Global Trade Item Number

SKUGTIN
O3757-5ML04061837602054

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