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Merck
CN

251747

Sigma-Aldrich

辛基缩水甘油醚

98%

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别名:
2-乙基己基缩水甘油醚, 3-环氧丙烷
经验公式(希尔记法):
C11H22O2
CAS号:
分子量:
186.29
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

98%

形式

liquid

折射率

n20/D 1.434 (lit.)

bp

60-62 °C/0.3 mmHg (lit.)

密度

0.891 g/mL at 25 °C (lit.)

SMILES字符串

CCCCC(CC)COCC1CO1

InChI

1S/C11H22O2/c1-3-5-6-10(4-2)7-12-8-11-9-13-11/h10-11H,3-9H2,1-2H3

InChI key

BBBUAWSVILPJLL-UHFFFAOYSA-N

应用

  • Solution properties of N-(2-allyl-butyl ether)-O-carboxymethyl chitosan and N-(2-allyl-isooctyl ether)-O-carboxymethyl chitosan.: This study explores the solution properties and potential applications of modified chitosan derivatives. It highlights their use in creating biocompatible coatings and medical device adhesives due to their enhanced solubility and functional properties (Liu et al., 2021).
  • All-Polycarbonate Thermoplastic Elastomers Based on Triblock Copolymers Derived from Triethylborane-Mediated Sequential Copolymerization of CO(2) with Various Epoxides.: This research details the development of thermoplastic elastomers using 2-Ethylhexyl glycidyl ether as a monomer. These materials show promise in life science manufacturing for creating advanced epoxy systems and low viscosity epoxy resin modifiers (Jia et al., 2020).
  • O-Carboxymethyl chitosan-based pH-responsive amphiphilic chitosan derivatives: Characterization, aggregation behavior, and application.: This paper discusses the creation of pH-responsive chitosan derivatives for use in biocompatible coatings and medical device adhesives. The modifications with 2-Ethylhexyl glycidyl ether improve their functionality and application potential in the medical field (Liu et al., 2020).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Irrit. 2 - Skin Sens. 1

WGK

WGK 2

闪点(°F)

206.6 °F

闪点(°C)

97 °C

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Xiaofei Zhang et al.
Science advances, 6(17), eaaz4824-eaaz4824 (2020-05-20)
CO2 cycloaddition with epoxides at low temperature and pressure has been broadly recognized as an ambitious but challenging goal, which requires the catalysts to have precisely controlled Lewis acid sites. Here, we demonstrate that both stereochemical environment and oxidation state

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