2-Ethylhexyl acrylate
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| Names | |
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| Preferred IUPAC name
2-Ethylhexyl prop-2-enoate | |
| Other names
2-Ethylhexyl acrylate
2-EHA | |
| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | 100.002.801 |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C11H20O2 | |
| Molar mass | 184.279 g·mol−1 |
| Hazards | |
| GHS labelling: | |
 [1]
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| Warning | |
| H315, H317, H335, H412[1] | |
| P273, P280, P304+P340+P312, P333+P313[1] | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Ethylhexyl acrylate is a colorless liquid acrylate with a sweet odor.
Preparation
Racemic 2-ethylhexyl acrylate can be prepared with a high yield by esterification of acrylic acid with racemic 2-ethylhexanol in the presence of hydroquinone as a polymerization inhibitor and a strong acid such as methanesulfonic acid by reactive distillation using toluene as an azeotroping agent.[2]
Properties
2-Ethylhexyl acrylate polymerizes easily. The polymerization can be initiated by light, peroxides, heat, or contaminants. It can react violently when combined with strong oxidants and can form explosive mixtures with air at temperatures above 82 °C (180 °F). The chemical, physical, and toxicological properties, however, can be greatly modified by additives or stabilizers.
Use
2-Ethylhexyl acrylate and butyl acrylate are the major base monomers for the preparation of acrylate adhesives. 2-Ethylhexyl acrylate can react by free-radical polymerization to form macromolecules having a molecular weight of up to 200,000 g/mol. Other monomers such as vinyl acetate, methyl acrylate, and styrene may be copolymerized to modify the properties of the resulting polymer.[3]
References
- ^ a b c Record of 2-Ethylhexyl acrylate in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 11 March 2020.
- ^ US 2917538, R.L. Carlyle, "Process for the production of acrylic acid esters", published 1959-12-15, assigned to The Dow Chemical Co.
- ^ Bodo Müller, Walter Rath, Walter Rath: Formulierung von Kleb- und Dichtstoffen. 1. Auflage. Vincentz Network, Hannover 2004, ISBN 3878707916, S. 235 ([1], p. 235, at Google Books).