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Methyl acrylate can be prepared by debromination of methyl 2,3-dibromopropanoate with zinc. [10] Methyl acrylate is formed in good yield on pyrolysis of methyl lactate in the presence of ethenone (ketene). [11] Methyl lactate is a renewable "green chemical". Another patent [12] describes the dehydration of methyl lactate over zeolites.
Methyl acrylate; The anion of methacrylic acid This page was last edited on 4 February 2015, at 16:22 (UTC). Text is available under the Creative Commons Attribution ...
The acrylate ion is the anion CH 2 =CHCO − 2. Often, acrylate refers to esters of acrylic acid, the most common member being methyl acrylate. These acrylates contain vinyl groups. These compounds are of interest because they are bifunctional: the vinyl group is susceptible to polymerization and the carboxylate group carries myriad ...
Acrylate polymers are derived from but do not contain the acrylate group. [4] The carboxyl group of acrylic acid can react with ammonia to form acrylamide, or with an alcohol to form an acrylate ester. Acrylamide and methyl acrylate are commercially important examples of α,β-unsaturated amides and α,β-unsaturated esters, respectively. They ...
Poly(methyl acrylate) (PMA) is a family of organic polymers with the formula (CH 2 CHCO 2 CH 3) n. It is a synthetic acrylate polymer derived from methyl acrylate monomer. The polymers are colorless. This homopolymer is far less important than copolymers derived from methyl acrylate and other monomers.
In terms of the acute toxicity of methyl methacrylate, the LD 50 is 7–10 g/kg (oral, rat). It is an irritant to the eyes and can cause redness and pain. [16] [17] Irritation of the skin, eye, and nasal cavity has been observed in rodents and rabbits exposed to relatively high concentrations of methyl methacrylate. Methyl methacrylate is a ...
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Base catalysed Michael addition of methyl acrylate to 2,6-di-tert-butylphenol forms the intermediate butyl-phloretic ester. High temperature transesterification of this with pentaerythritol gives the final product. Driving this reaction to completion can be difficult and commercial samples often contain low levels of the tri-ester.