251747
2-Ethylhexyl glycidyl ether
98%
Synonym(s):
2-Ethyl hexyleneglycidyl ether, 3-epoxypropane, Glycidyl 2-ethylhexyl ether
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About This Item
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Assay
98%
form
liquid
refractive index
n20/D 1.434 (lit.)
bp
60-62 °C/0.3 mmHg (lit.)
density
0.891 g/mL at 25 °C (lit.)
SMILES string
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
Related Categories
Application
- 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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
206.6 °F - closed cup
Flash Point(C)
97 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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