P8925
Octaethylene glycol monododecyl ether
≥98% (GC)
Synonym(s):
C12E8, Dodecyl octaethylene glycol ether, Dodecyloctaglycol, Polyoxyethylene (8) lauryl ether
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About This Item
Linear Formula:
CH3(CH2)11(OCH2CH2)8OH
CAS Number:
Molecular Weight:
538.75
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1893466
description
non-ionic
Quality Level
assay
≥98% (GC)
form
solid
mol wt
average mol wt 66,000
aggregation number
123
CMC
0.11
SMILES string
CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCO
InChI
1S/C28H58O9/c1-2-3-4-5-6-7-8-9-10-11-13-30-15-17-32-19-21-34-23-25-36-27-28-37-26-24-35-22-20-33-18-16-31-14-12-29/h29H,2-28H2,1H3
InChI key
YYELLDKEOUKVIQ-UHFFFAOYSA-N
General description
Octaethylene glycol monododecyl ether is a nonionic detergent.
Application
Detergent used for the study of membrane proteins in a native-like state, e.g. ATPase. Used in a mixed micellar assay for lipoxygenase acting at neutral pH and for functional reconstitution of influenza virus envelopes.
Octaethylene glycol monododecyl ether has been used in a study to assess intestinal sodium transport mechanisms. It has also been used in a study to investigate interactions between dyes and surfactants in inkjet ink used for textiles.
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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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Ju-Young Park et al.
Journal of oleo science, 60(12), 627-637 (2011-11-30)
Optimal preparation of inkjet ink should be possible through the elucidation of the relationship between dye/additive interactions and ink performance. In the present study, the interactions between the dyes and surfactant additives were investigated. To investigate the physical properties of
Cleyton C Domingues et al.
The Journal of membrane biology, 234(3), 195-205 (2010-03-27)
Transient lateral microdomains or lipid rafts play important roles in many physiological membrane-mediated cell processes. Detergent-resistant membranes (DRMs) are good models for the study of lipid rafts. Here we report that DRMs can be obtained by treating human erythrocytes with
L Tortech et al.
Biochimica et biophysica acta, 1514(1), 76-86 (2001-08-22)
Many attempts have been made to rationalize the use of detergents for membrane protein studies [J. Biol. Chem. 264 (1989) 4907]. The barrier properties of the detergent headgroup may be one parameter critically involved in protein protection. In this paper