2-Ethylhexyl acrylate

2-ethylhexyl acrylate.svg 200px 2-Ethylhexyl prop-2-enoate 2-Ethylhexyl acrylate2-EHA 103-11-7 correct CAS correct FDA HR49R9S6XG 7636 CCCCC(CC)COC(=O)C=C C19420 203-080-7 InChI=1S/C11H20O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h6,10H,3-5,7-9H2,1-2H3 GOXQRTZXKQZDDN-UHFFFAOYSA-N 7354 82465 11 20 2 colorless liquid 0.885 g/mL -90 215-219 organic solvents exclamation mark15610 103-11-7 2-Ethylhexyl acrylate 11 March 2020 Warning 315 317 335 412 273 280 304+340+312 333+313 180 496 2-Ethylhexyl acrylate is a colorless liquid acrylate used in the making of paints,2-ETHYLHEXYL ACRYLATE https://cameochemicals.noaa.gov/chemical/8674 April 22, 2024 CAMEO Chemicals plastics7636 2-Ethylhexyl acrylate (compound) and adhesives.Heatley Frank Lovell Peter A. Yamashita Tsuyoshi 2001-10-01 Chain Transfer to Polymer in Free-Radical Solution Polymerization of 2-Ethylhexyl Acrylate Studied by NMR Spectroscopy https://pubs.acs.org/doi/10.1021/ma0101299 Macromolecules en 34 22 7636–7641 10.1021/ma0101299 0024-9297 subscription It has an odor that has been variously described as pleasant2-Ethylhexyl acrylate https://pubchem.ncbi.nlm.nih.gov/compound/2-Ethylhexyl-acrylate April 22, 2024 PubChem or acrid and musty.Shah Yogi January 1995 2-Ethylhexyl acrylate https://www.osha.gov/sites/default/files/methods/osha-pv2026.pdf Occupational Safety and Health Administration 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.US 2917538 Process for the production of acrylic acid esters 1959-12-15 1957-12-19 R.L. Carlyle The Dow Chemical Co. 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 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.Bodo Müller, Walter Rath: Formulierung von Kleb- und Dichtstoffen 1. Auflage. Vincentz Network, Hannover 2004, 3878707916, S. 235 (kSpLnuE3LqQC 235) References Category:Acrylate esters Category:2-Ethylhexyl esters