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Merck
CN

P4654

Sigma-Aldrich

Pentaethylene glycol monooctyl ether

别名:

C8E5, Octyl pentaethylene glycol ether, Octylpentaglycol

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About This Item

线性分子式:
CH3(CH2)7(OCH2CH2)5OH
CAS号:
分子量:
350.49
Beilstein:
1711907
MDL编号:
UNSPSC代码:
12161900
PubChem化学物质编号:
NACRES:
NA.25

描述

non-ionic

质量水平

方案

≥98.0% (GC)

分子量

350.49 g/mol

密度

0.99 g/mL at 25 °C (lit.)

SMILES字符串

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

InChI key

MJELOWOAIAAUJT-UHFFFAOYSA-N

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应用

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.

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)
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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