|Preferred IUPAC name
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||72.063 g·mol−1|
|Appearance||clear, colorless liquid|
|Melting point||14 °C (57 °F; 287 K)|
|Boiling point||141 °C (286 °F; 414 K)|
|Vapor pressure||3 mmHg|
|Acidity (pKa)||4.25 (H2O)|
|Viscosity||1.3 cP at 20 °C (68 °F)|
|Main hazards||Corrosive (C),|
Dangerous for the
|Safety data sheet||MSDS|
|R-phrases (outdated)||R10 R20/21/22 R35 R50|
|S-phrases (outdated)||S26 S36/37/39 S45 S61|
|Flash point||68 °C (154 °F; 341 K)|
|429 °C (804 °F; 702 K)|
|US health exposure limits (NIOSH):|
|TWA 2 ppm (6 mg/m3) [skin]|
IDLH (Immediate danger)
Related carboxylic acids
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Acrylic acid (IUPAC: propenoic acid) is an organic compound with the formula CH2=CHCOOH. It is the simplest unsaturated carboxylic acid, consisting of a vinyl group connected directly to a carboxylic acid terminus. This colorless liquid has a characteristic acrid or tart smell. It is miscible with water, alcohols, ethers, and chloroform. More than a million tons are produced annually.
- CH2=CHCH3 + 3⁄2 O2 → CH2=CHCO2H + H2O
Because acrylic acid and its esters have long been valued commercially, many other methods have been developed, but most have been abandoned for economic or environmental reasons. An early method was the hydrocarboxylation of acetylene ("Reppe chemistry"):
Acrylic acid was once manufactured by the hydrolysis of acrylonitrile, a material derived from propene by ammoxidation, but this route was abandoned because ir cogenerates ammonium side products, which must be disposed of. Other now abandoned precursors to acrylic acid include ethenone and ethylene cyanohydrin.
Dow Chemical Company and its partner OPX Biotechnologies are investigating using fermented sugar to produce 3-hydroxypropionic acid (3HP), an acrylic-acid precursor. The goal is to reduce greenhouse-gas emissions.
Reactions and uses
Acrylic acid undergoes the typical reactions of a carboxylic acid. When reacted with an alcohol, it forms the corresponding ester. The esters and salts of acrylic acid are collectively known as acrylates (or propenoates). The most common alkyl esters of acrylic acid are methyl, butyl, ethyl, and 2-ethylhexyl acrylate.
Acrylic acid and its esters readily combine with themselves (to form polyacrylic acid) or other monomers (e.g. acrylamides, acrylonitrile, vinyl compounds, styrene, and butadiene) by reacting at their double bond, forming homopolymers or copolymers, which are used in the manufacture of various plastics, coatings, adhesives, elastomers, as well as floor polishes and paints.
Acrylic acid is a compound, which is used in many industries like the diaper industry, the water treatment industry or the textiles industry. On a worldwide scale the consumption rate of acrylic acid is projected to reach more than an estimated 8,000 kilo tons, by 2020. This increase is expected to occur as a result of using this product in new applications, including personal care products, detergents and products that are used for adult incontinence.
As a substituent acrylic acid can be found as an acyl group or a carboxyalkyl group, depending on the removal of the group from the molecule. More specifically, these are:
- The acryloyl group, with the removal of the −OH from carbon-1.
- The 2-carboxyethenyl group, with the removal of a −H from carbon-3. This substituent group is found in chlorophyll.
Acrylic acid is severely irritating and corrosive to the skin and the respiratory tract. Eye contact can result in severe and irreversible injury. Low exposure will cause minimal or no health effects, while high exposure could result in pulmonary edema. The LD50 is 340 mg/kg (rat, oral).
- Merck Index, 11th Edition, 124.
- NIOSH Pocket Guide to Chemical Hazards. "#0013". National Institute for Occupational Safety and Health (NIOSH).
- "Acrylic acid_msds".
- Dippy, J. F. J.; Hughes, S. R. C.; Rozanski, A. (1959). "The dissociation constants of some symmetrically disubstituted succinic acids". Journal of the Chemical Society: 2492–2498. doi:10.1039/JR9590002492.
- Takashi Ohara, Takahisa Sato, Noboru Shimizu, Günter Prescher Helmut Schwind, Otto Weiberg, Klaus Marten, Helmut Greim (2003), "Acrylic Acid and Derivatives", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a01_161.pub2CS1 maint: Multiple names: authors list (link)
- Naumann d'Alnoncourt, Raoul; Csepei, Lénárd-István; Hävecker, Michael; Girgsdies, Frank; Schuster, Manfred E.; Schlögl, Robert; Trunschke, Annette (2014). "The reaction network in propane oxidation over phase-pure MoVTeNb M1 oxide catalysts" (PDF). Journal of Catalysis. 311: 369–385. doi:10.1016/j.jcat.2013.12.008. hdl:11858/00-001M-0000-0014-F434-5. Archived from the original (PDF) on 2016-02-15. Retrieved 2017-07-15.
- Sakakura, Toshiyasu; Choi, Jun-Chul; Yasuda, Hiroyuki (13 June 2007). "Transformation of Carbon dioxide". Chemical Reviews. 107 (6): 2365–2387. doi:10.1021/cr068357u. PMID 17564481.
- Sweet Deal: Dow and Partner Cook up Sugar-to-Acrylic Plan. Durabilityanddesign.com. Retrieved on 2012-05-24.
- Better Bugs to Make Plastics, Technology Review, September 20, 2010, retrieved January 9, 2012. Technologyreview.com (2010-09-20). Retrieved on 2012-05-24.
- "Acrylic acid market". Retrieved 2018-05-30.
- Talhout, Reinskje; Schulz, Thomas; Florek, Ewa; Van Benthem, Jan; Wester, Piet; Opperhuizen, Antoon (2011). "Hazardous Compounds in Tobacco Smoke". International Journal of Environmental Research and Public Health. 8 (12): 613–628. doi:10.3390/ijerph8020613. ISSN 1660-4601. PMC 3084482. PMID 21556207.