Ethyl methacrylate explained

Ethyl methacrylate is the organic compound with the formula C2H5O2CC(CH3)=CH2. A colorless liquid, it is a common monomer for the preparation of acrylate polymers.[1] It is typically polymerized under free-radical conditions.[2]

Ethyl methacrylate was first obtained by treating ethyl 2-hydroxyisobutyrate with phosphorus pentachloride in an apparent dehydration reaction.[3]

Environmental issues and health hazards

The related methyl and butyl methacrylates have respective acute LD50s 10 and 20 g/kg (oral, rat);[1] a linear extrapolation suggests that ethyl methacrylate would have LD50 approximately 13 g/kg.

Acrylate esters irritate the eyes and can cause blindness.[1]

See also

References

  1. .
  2. Controlled Radical Polymerization of Methacrylic Monomers in the Presence of a Bis(ortho-chelated) Arylnickel(II) Complex and Different Activated Alkyl Halides. Granel, C.. Dubois . Ph.. Jérôme . R.. Teyssié . Ph.. Macromolecules. 1996. 29. 27. 8576–8582. 10.1021/ma9608380. 1996MaMol..29.8576G.
  3. Justus Liebigs Annalen der Chemie. 136. 12. Untersuchungen über Säuren aus der Acrylsäure-Reihe; 1) Umwandlung der Säuren aus der Milchsäure-Reihe in die der Acrylsäure-Reihe. E. Frankland, B. F. Duppa. 1865. 10.1002/jlac.18651360102.