Acrylates (
IUPAC
The International Union of Pure and Applied Chemistry (IUPAC ) is an international federation of National Adhering Organizations working for the advancement of the chemical sciences, especially by developing nomenclature and terminology. It is ...
: prop-2-enoates) are the
salt
In common usage, salt is a mineral composed primarily of sodium chloride (NaCl). When used in food, especially in granulated form, it is more formally called table salt. In the form of a natural crystalline mineral, salt is also known as r ...
s,
ester
In chemistry, an ester is a compound derived from an acid (either organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group () of that acid is replaced by an organyl group (R). These compounds contain a distin ...
s, and
conjugate bases of
acrylic acid. The acrylate ion is the anion . Often, acrylate refers to
ester
In chemistry, an ester is a compound derived from an acid (either organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group () of that acid is replaced by an organyl group (R). These compounds contain a distin ...
s 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 functionalities.
Monomers
Acrylates are defined by the formula , where R can be many groups:
*
Acrylic acid
*
Methyl acrylate
*
Ethyl acrylate
* 2-Chloroethyl vinyl ether
*
2-Ethylhexyl acrylate
*
Butyl acrylate
*
Trimethylolpropane triacrylate (TMPTA)
The versatility of the resulting polymers is owed to the range of R groups.
File:Acrylate-anion.svg, The acrylate anion
File:Trimethylolpropane triacrylate.svg, Trimethylolpropane triacrylate (TMPTA), a trifunctional acrylate ester
File:Methylacrylat.svg, Methyl acrylate, an acrylic ester
File:Hexandioldiacrylat.svg, Hexandiol diacrylate, a bifunctional acrylate
File: Pentaerythritol tetraacrylate.png, Pentaerythritol tetraacrylate (PETA), a tetrafunctional acrylate
File:Polyacrylate.svg, A generic polyacrylate
Acrylate derivatives
Methacrylates ( ) and
cyanoacrylates ( ,) are closely related to acrylates. The feature a methyl and a nitrile in place of the H alpha to the carboxy functional group. They share several properties, being polymerized by radicals and being colorless.
File:Methyl-methacrylate-skeletal.svg, Methyl methacrylate, precursor to "perspex" (plexiglass)
File:Ethyl cyanoacrylate.svg, Ethyl cyanoacrylate, precursor to "super glue"
Polymers

Some acrylate polymers (
poly(methyl methacrylate) etc. not included):
*
Poly(methyl acrylate) (PMA)
*
Poly(ethyl acrylate) (PEA)
*
Poly(butyl acrylate) (PBA)
Acrylate
monomer
A monomer ( ; ''mono-'', "one" + '' -mer'', "part") is a molecule that can react together with other monomer molecules to form a larger polymer chain or two- or three-dimensional network in a process called polymerization.
Classification
Chemis ...
s are used to form acrylate polymers. Most commonly, these polymers are in fact copolymers, being derived from two monomers.
Related polymers

In the same way that several variants of acrylic esters are known, so too are the corresponding polymers. Their properties strongly depends on the substituent.
A large family of acrylate-like polymers are derived from
methyl methacrylate and many related esters, especially
polymethyl methacrylate.
A second large family of acrylate-like polymers are derived from
ethyl cyanoacrylate, which gives rise to
cyanoacrylates.
Yet another family of acrylate-related polymers are the
polyacrylamides, especially the parent derived from
acrylamide.
Other uses
In addition to forming polymers, acrylate esters participate in other reactions relevant to organic chemistry. They are
Michael acceptors and
dienophiles. They undergo
transesterification.
Production
Acrylates are industrially prepared by treating acrylic acid with the corresponding alcohol in presence of a catalyst. The reaction with lower alcohols (
methanol,
ethanol
Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula . It is an Alcohol (chemistry), alcohol, with its formula also written as , or EtOH, where Et is the ps ...
) takes place at 100–120 °C with acidic
heterogeneous catalysts (
cation exchanger). The reaction of higher alcohols (
''n''-butanol,
2-ethylhexanol) is catalysed with
sulfuric acid
Sulfuric acid (American spelling and the preferred IUPAC name) or sulphuric acid (English in the Commonwealth of Nations, Commonwealth spelling), known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, ...
in homogeneous phase. Acrylates of even higher alcohols are obtainable by
transesterification of lower esters catalysed by
titanium alcoholates or
organic tin compounds (e.g.
dibutyltin dilaurate).
See also
*
Acrylate polymer
*
Sodium polyacrylate thickeners
*
Methacrylate
References
{{Authority control
Carboxylate anions
Monomers
Acrylate esters