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Merck

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:
3055-98-9
Molecular Weight:
538.75
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24898996
MDL number:
MFCD00043234
Beilstein/REAXYS Number:
1893466

Product Name

Octaethylene glycol monododecyl ether, ≥98% (GC)

InChI key

YYELLDKEOUKVIQ-UHFFFAOYSA-N

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

description

non-ionic

assay

≥98% (GC)

form

solid

mol wt

average mol wt 66,000

aggregation number

123

CMC

0.11

Quality Level

100

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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.

General description

Octaethylene glycol monododecyl ether is a nonionic detergent.

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
MKCV9655
MKCQ7795
MKCK1820
MKCC2887
MKBT3049V

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Cédric Montigny et al.
Biochemical and biophysical research communications, 391(1), 1067-1069 (2009-12-17)
Many membrane proteins become labile when they are solubilized by detergent. Here we show that the presence of high concentrations of glycyl betaine stabilizes one of these proteins, the sarcoplasmic reticulum Ca(2+)-ATPase (SERCA1a), solubilized with nonionic detergents like n-dodecyl beta-d-maltopyranoside
[Relationship between activity and tetraprotomeric structure of ion-transporting ATPases].
Kazuhiro Abe et al.
Seikagaku. The Journal of Japanese Biochemical Society, 79(6), 527-534 (2007-08-01)
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
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
G C Troiano et al.
Biophysical journal, 75(2), 880-888 (1998-07-24)
The effects of a nonionic surfactant, octaethyleneglycol mono n-dodecyl ether (C12E8), on the electroporation of planar bilayer lipid membranes made of the synthetic lipid 1-pamitoyl 2-oleoyl phosphatidylcholine (POPC), was studied. High-amplitude ( approximately 100-450 mV) rectangular voltage pulses were used
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