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Merck
CN

P4654

Pentaethylene glycol monooctyl ether

别名:

C8E5, Octyl pentaethylene glycol ether, Octylpentaglycol

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关于此项目

线性分子式:
CH3(CH2)7(OCH2CH2)5OH
化学文摘社编号:
分子量:
350.49
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1711907
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InChI key

MJELOWOAIAAUJT-UHFFFAOYSA-N

SMILES string

CCCCCCCCOCCOCCOCCOCCOCCO

InChI

1S/C18H38O6/c1-2-3-4-5-6-7-9-20-11-13-22-15-17-24-18-16-23-14-12-21-10-8-19/h19H,2-18H2,1H3

description

non-ionic

assay

≥98.0% (GC)

mol wt

350.49 g/mol

density

0.99 g/mL at 25 °C (lit.)

Quality Level

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Application

Pentaethylene glycol monooctyl ether has been used to study the size and morphology of aggregates. It has also been used in a study to investigate the sorption of monodisperse alcohol ethoxylates and their effects on the mobility of 2,4-D in isolated plant cuticles.

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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Study of the size and morphology of aggregates formed by pentaethylene glycol monooctyl ether (C"8EO"5) in n-heptane
Sandoval, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 17-23 (2012)
Sorption of Monodisperse Alcohol Ethoxylates and Their Effects on the Mobility of 2,4-D in Isolated Plant Cuticles
Riederer, M., et al.
Journal of Agricultural and Food Chemistry, 43, 1067-1075 (1995)
D R Bristow et al.
Journal of neurochemistry, 48(5), 1537-1540 (1987-05-01)
The detergent n-octylpentaoxyethylene is one in the series of tenside detergents developed for membrane solubilisation. We have used this detergent to solubilise benzodiazepine receptors from rat cerebellum. The soluble receptor has an affinity (KD) for [3H]flunitrazepam of 1.8 nM +/-
Maria K Janowska et al.
Protein science : a publication of the Protein Society, 25(1), 286-294 (2015-09-04)
β-synuclein (βS) is a homologue of α-synuclein (αS), the major protein component of Lewy bodies in patients with Parkinson's disease. In contrast to αS, βS does not form fibrils, mitigates αS toxicity in vivo and inhibits αS fibril formation in

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