Difference between revisions of "Ethyl acrylate"

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== Description ==
 
== Description ==
  
A colorless, acrid smelling liquid primarily used as a monomer for the production as [http://cameo.mfa.org/materials/fullrecord.asp?name=acrylic resin acrylic] polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most [http://cameo.mfa.org/materials/fullrecord.asp?name=solvent solvents]. Ethyl acrylate monomer is used in water [http://cameo.mfa.org/materials/fullrecord.asp?name=emulsion emulsion] paints and for coatings on [http://cameo.mfa.org/materials/fullrecord.asp?name=textile textiles], [http://cameo.mfa.org/materials/fullrecord.asp?name=paper paper], and [http://cameo.mfa.org/materials/fullrecord.asp?name=leather leather].
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A colorless, acrid smelling liquid primarily used as a monomer for the production as [http://cameo.mfa.org/materials/fullrecord.asp?name=acrylic%20resin acrylic] polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most [http://cameo.mfa.org/materials/fullrecord.asp?name=solvent solvents]. Ethyl acrylate monomer is used in water [http://cameo.mfa.org/materials/fullrecord.asp?name=emulsion emulsion] paints and for coatings on [http://cameo.mfa.org/materials/fullrecord.asp?name=textile textiles], [http://cameo.mfa.org/materials/fullrecord.asp?name=paper paper], and [http://cameo.mfa.org/materials/fullrecord.asp?name=leather leather].
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'thyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)
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2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'éthyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)
  
 
[[[SliderGallery rightalign|ethyl acrylate.jpg~Chemical structure]]]
 
[[[SliderGallery rightalign|ethyl acrylate.jpg~Chemical structure]]]
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== Authority ==
 
== Authority ==
  
* Susan Budavari (ed.), ''The Merck Index'', Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996  Comment: entry 3805
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* ''The Merck Index'', Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996  Comment: entry 3805
  
* Richard S. Lewis, Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
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* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Revision as of 06:53, 24 July 2013

Description

A colorless, acrid smelling liquid primarily used as a monomer for the production as acrylic polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most solvents. Ethyl acrylate monomer is used in water emulsion paints and for coatings on textiles, paper, and leather.

Synonyms and Related Terms

2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'éthyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)

Chemical structure

Ethyl acrylate.jpg


Other Properties

Soluble in ethanol, ether.

Composition CH2:CHCOOC2H5
CAS 140-88-5
Melting Point -72
Density 0.9405
Molecular Weight mol. wt. = 100.1
Boiling Point 99.4

Hazards and Safety

Toxic by ingestion, inhalation and skin contact. Skin contact will cause irritation. Suspected carcinogen. Flammable. Flash point = 9C

LINK: International Chemical Safety Card

Authority

  • The Merck Index, Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996 Comment: entry 3805
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993

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