metyl acrylat

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Methyl acrylate
Skeletal formula of methyl Acrylate
Ball-and-stick model of the methyl acrylate molecule
Preferred IUPAC name

Methyl prop-2-enoate[1]

Other names

Methyl acrylate
Methyl propenoate
Curithane 103[1]


CAS Number

  • 96-33-3 check

3D model (JSmol)

  • Interactive image
  • ChEMBL9019 check
  • 7022 check
ECHA InfoCard 100.002.274 Edit this at Wikidata
  • C19443 ☒

PubChem CID

  • 7294
  • WC487PR91H check

CompTox Dashboard (EPA)

  • DTXSID0024183 Edit this at Wikidata


  • InChI=1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3 check



  • C=CC(OC)=O


Chemical formula

Molar mass 86.090 g·mol−1
Appearance Colorless liquid
Odor Acrid[2]
Density 0.95 g/cm3[3]
Melting point −74 °C (−101 °F; 199 K)[3]
Boiling point 80 °C (176 °F; 353 K)[3]

Solubility in water

5 g/100 mL
Vapor pressure 65 mmHg (20°C)[2]
  • 0.391 mPa·s at 35 °C[4]
  • 0.333 mPa·s at 45 °C[4]
Occupational safety and health (OHS/OSH):

Main hazards

Harmful (Xn); Highly flammable (F+)
Flash point −3 °C (27 °F; 270 K)[3]
Explosive limits 2.8–25%[2]
Lethal dose or concentration (LD, LC):

LC50 (median concentration)

3575 ppm (mouse)
1350 ppm (rat, 4 hr)
1000 ppm (rat, 4 hr)
2522 ppm (rabbit, 1 hr)[5]
NIOSH (US health exposure limits):

PEL (Permissible)

TWA 10 ppm (35 mg/m3) [skin][2]

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REL (Recommended)

TWA 10 ppm (35 mg/m3) [skin][2]

IDLH (Immediate danger)

250 ppm[2]
Safety data sheet (SDS) Oxford MSDS

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Infobox references

Methyl acrylate is an organic compound, more accurately the methyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced to tướng make acrylate fiber, which is used to tướng weave synthetic carpets.[6] It is also a reagent in the synthesis of various pharmaceutical intermediates. Owing to tướng the tendency of methyl acrylate to tướng polymerize, samples typically contain an inhibitor such as hydroquinone.


The standard industrial reaction for producing methyl acrylate is esterification with methanol under acid catalysis (sulfuric acid, p-toluenesulfonic acid or acidic ion exchangers.[7]). The transesterification is facilitated because methanol and methyl acrylate size a low boiling azeotrope (boiling point 62–63 °C).[8]

The patent literature[9] describes a one-pot route involving vapor-phase oxidation of propene or 2-propenal with oxygen in the presence of methanol.

Other methods[edit]

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.

The nickel tetracarbonyl-catalyzed hydrocarboxylation of acetylene with carbon monoxide in the presence of methanol also yields methyl acrylate.[13] The reaction of methyl formate with acetylene in the presence of transition metal catalysts also leads to tướng methyl acrylate.[14] Both, the alcoholysis of propiolactone with methanol as well as the methanolysis of acrylonitrile via intermediately formed acrylamide sulfate[15] are also proven but obsolete processes.


Methyl acrylate is after butyl acrylate and ethyl acrylate the third most important acrylic ester with a worldwide annual production of about 200,000 tons in 2007.[16] Poly(methyl acrylate) is a tacky material near room temperature, and as such it is not particularly useful as a structural material. Commonly, methyl acrylate (and other acrylate esters) are copolymerized with other alkenes to tướng give useful engineering plastics.[17] A variety of vinyl monomers are used, including styrene and other acrylates.[18] The resulting copolymers give acrylic paints that are harder and more brittle kêu ca those with the homologous acrylates. Copolymerizing methyl acrylate with acrylonitrile improves their melt processability to tướng fibers, which could be used as precursors for carbon fibers.[19] Methyl acrylate is the precursor to tướng fibers that are woven to tướng make carpets.

Amino derivatives[edit]

Methyl acrylate reacts catalysed by Lewis bases in a Michael addition with amines in high yields to tướng β-alanine derivatives which provide amphoteric surfactants when long-chain amines are used and the ester function is hydrolysed subsequently.

Acrylates are also used in the preparation of poly(amidoamine) (PAMAM) dendrimers typically by Michael addition with a primary amine.

Amphotere beta-alanine

Methyl acrylate is used for the preparation of 2-dimethylaminoethyl acrylate by transesterification with dimethylaminoethanol in significant quantities of over 50,000 tons / year.[20]


Methyl acrylate is a classic Michael acceptor, which means that it adds nucleophiles at its terminus. For example, in the presence of a base catalyst, it adds hydrogen sulfide to tướng give the thioether:[21]

2 CH2CHCO2CH3 + H2S → S(CH2CH2CO2CH3)2

It is also a good dienophile.


It is an acute toxin with an LD50 (rats, oral) of 300 mg/kg and a TLV of 10 ppm.

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  1. ^ a b "methyl acrylate - Compound Summary". PubChem. Retrieved June 30, 2012.
  2. ^ a b c d e f NIOSH Pocket Guide to tướng Chemical Hazards. "#0394". National Institute for Occupational Safety and Health (NIOSH).
  3. ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  4. ^ a b George, John; Sastry, Nandhibatla V.; Patel, Sunil R.; Valand, Mahendra K. (2002). "Densities, Viscosities, Speeds of Sound, and Relative Permittivities for Methyl Acrylate + 1-Alcohols (C1−C6) atT= (308.15 and 318.15) K". Journal of Chemical & Engineering Data. American Chemical Society (ACS). 47 (2): 262–269. doi:10.1021/je010268l. ISSN 0021-9568.
  5. ^ "Methyl acrylate". Immediately Dangerous to tướng Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  6. ^ 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.pub2. ISBN 3527306730.{{cite encyclopedia}}: CS1 maint: uses authors parameter (link)
  7. ^ "Esterification: Acrylate esters (MA, EA, BA, MMA, 2-EHA)". Retrieved 2013-02-21.
  8. ^ Chessie E. Rehberg (1955). "n-Butyl acrylate". Organic Syntheses. 26: 18.; Collective Volume, vol. 3, p. 146
  9. ^ US 3925463, Ferlazzo, Natale; Buzzi, Gian Fausto & Ghirga, Marcello, "Process for the production of methyl acrylate", published 1975-12-09, assigned to tướng Societa' Italiana Resine S.I.R., S.p.A.
  10. ^ F. Beilstein: Handbuch der organischen Chemie, 3. Auflage, 1. Band. Verlag Leopold Voss, 1893, S. 501. Volltext.
  11. ^ US 2417748, Hagemeyer, Hugh J., "Preparation of methyl acrylate", published 1947-03-18, assigned to tướng Eastman Kodak Company
  12. ^ US 5250729, Abe, Takafumi & Hieda, Shinichi, "Process for preparing unsaturated carboxylic acid or ester thereof", published 1993-10-05, assigned to tướng Tập đoàn Mitsubishi Gas Chemical Company
  13. ^ W. Reppe, J. Liebigs Ann. Chem., 582 (1), 116-132 (1953)
  14. ^ US 6022990, Liu, Zhao-Tie; Zhang, Jia-Qi & Yang, Xian-Gui, "Method for synthesizing methyl acrylate", published 2000-02-08, assigned to tướng Chengdu Institute of Organic Chemistry and National Research and Engineering Centre for Coal Slurry Gasification and Coal Chemical Industry
  15. ^ H.-J. Arpe, Industrielle Organische Chemie, 6. Aufl., Wiley-VCH Verlag, Weinheim, 2007, ISBN 978-3-527-31540-6.
  16. ^ CEH Marketing Research Report Acrylic Acid and Esters, SRI Consulting, July 2007.
  17. ^ Penzel, Erich; Ballard, Nicholas; Asua, José M. (2018). "Polyacrylates". Ullmann's Encyclopedia of Industrial Chemistry. pp. 1–20. doi:10.1002/14356007.a21_157.pub2. ISBN 9783527306732.
  18. ^ DOW Methyl acrylate, Product Safety Assessment
  19. ^ V. A. Bhanu; et al. (2002), "Synthesis and characterization of acrylonitrile methyl acrylate statistical copolymers as melt processable carbon fiber precursors" (PDF), Polymer (in German), vol. 43, no. 18, pp. 4841–4850, doi:10.1016/S0032-3861(02)00330-0
  20. ^ WO 2010136696, Paul, Jean-Michel; Tonnelier, Boris & Augustin, Francis, "Composition including dialkyl tin cậy oxide and use thereof as a transesterification catalyst for the synthesis of (meth)acrylic esters", published 2010-12-02, assigned to tướng Arkema
  21. ^ Edward A. Fehnel and Marvin Carmack (1950). "Methyl-β-dipropionate". Organic Syntheses. 30: 65.; Collective Volume, vol. 4, p. 669