- Product Name:
- Methyl acrylate
- Acrylate de methyle
- ACRYLIC ACID METHYL ESTER
- AKOS BBS-00004387
- METHYL PROPENOATE
- METHYL ACRYLATE
- METHYL 2-PROPENOATE
- 2-PROPENOIC ACID METHYL ESTER
- Product Categories:
- ester series
- Alpha Sort
- Analytical Standards
- Chemical Class
- EstersOther Lipid Related Products
- Fatty AcidsVolatiles/ Semivolatiles
- Lipid Analytical Standards
- META - METHGasoline, Diesel,&Petroleum
- Substance classes
- AcrylateCarbonyl Compounds
- Acrylic Monomers
- C2 to C5
- Carbonyl Compounds
- Mol File:
Methyl acrylate Chemical Properties
- Melting point:
- -75 °C
- Boiling point:
- 80 °C(lit.)
- 0.956 g/mL at 25 °C(lit.)
- vapor density
- 3 (vs air)
- vapor pressure
- 67.5 mm Hg ( 20 °C)
- refractive index
- n20/D 1.402(lit.)
- Flash point:
- 26.6 °F
- storage temp.
- Refrigerator (+4°C) + Flammables area
- explosive limit
- Odor Threshold
- Water Solubility
- 60 g/L (20 ºC)
- Light Sensitive
- Henry's Law Constant
- (x 10-4 atm?m3/mol): 1.3 at 20 °C (approximate - calculated from water solubility and vapor pressure)
- Exposure limits
- TLV-TWA 10 ppm (～35 mg/m3) (ACGIH and MSHA), TLV-TWA skin 10 ppm (～35 mg/m3) (OSHA); IDLH 1000 ppm (NIOSH).
- Stable. Incompatible with bases, acids, oxidizing agents, peroxides. May polymerize on exposure to light. Highly flammable. Commercial product may be inhibited by the presence of hydroquinone monomethyl ether.
- CAS DataBase Reference
- 96-33-3(CAS DataBase Reference)
- 2B (Vol. 39, Sup 7, 71, 122) 2019
- NIST Chemistry Reference
- 2-Propenoic acid, methyl ester(96-33-3)
- EPA Substance Registry System
- Methyl acrylate (96-33-3)
- Hazard Codes
- Risk Statements
- Safety Statements
- UN 1919 3/PG 2
- WGK Germany
- Autoignition Temperature
- 874 °F
- HS Code
- 2916 12 00
- Hazardous Substances Data
- 96-33-3(Hazardous Substances Data)
- LD50 orally in rats: 0.3 g/kg (Smyth, Carpenter)
Methyl acrylate Usage And Synthesis
Methyl acrylate is an organic compound with the formula CH2CHCO2CH3. It is the methyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced to make acrylate fiber, which is used to weave synthetic carpets. It is also a reagent in the synthesis of various pharmaceutical intermediates.
Methyl acrylate is a clear, colorless, corrosive liquid with a sharp, fruity odor. It is soluble in water and completely miscible with most organic solvents.
Methyl acrylate has a variety of industrial uses. the more important commercial uses of methyl acrylate include the preparation of thermoplastic coatings, use in the manufacture of acrylic and modacrylic fibers. In the fiber application, methyl acrylate is used as a comonomer with acrylonitrile. These acrylic fibers usually contain about 85% acrylonitrile and are used to fabricate clothing, blankets, carpets, and curtains. Other uses of methyl acrylate include coatings, adhesives, textile backcoatings, elastomers, plastics, and it is also found in ionic exchange resins, barrier film resins, antioxidant intermediates and acrylic fibers.
Clear, colorless, flammable liquid with a heavy, sweet, pungent odor. An odor threshold concentration of 3.5 ppbv was reported by Nagata and Takeuchi (1990).
Methyl acrylate is contained in some nail lacquers.
Acrylic polymers, amphoteric surfactants, vitamin B 1, chemical intermediate.
Methyl acrylate is a monomer used in themanufacture of plastic films, textiles, papercoatings, and other acrylate ester resins. It isalso used in amphoteric surfactants.
methacrylate: A salt or ester ofmethacrylic acid (2-methylpropenoicacid).
Acrylate esters can be produced in a number of ways. The most commonly used method, developed in 1970, involves a propylene oxidation process. The reaction occurs initially with the oxidation of propylene to acrolein, which in turn is oxidized to acrylic acid. Once the acrylic acid is formed, it is reacted with methanol which causes the formation of the methyl acrylate. This reaction is shown as follows:
An older method, the Reppe process, involves reacting acetylene with nickel carbonyl and methyl alcohol in the presence of an acid to produce methyl acrylate.
More recent methods for producing acrylate esters involve the use of organic carbonates as esterifying agents or isolating 2-halo- 1-alkenes from hydrocarbon feedstocks to produce the acrylate esters (Haggin, 1985).
Methyl acrylate is manufactured via a reaction of nickel carbonyl and acetylene with methanol in the presence of an acid; more commonly, however, it is manufactured via oxidation of propylene to acrolein and then to acrylic acid. The acid is reacted with methanol to yield the ester.
Colorless volatile liquid with an acrid odor. Flash point 27°F. Vapors may irritate the eyes and respiratory system. Highly toxic by inhalation, ingestion and skin absorption. Less dense than water (0.957 gm / cm3) and slightly soluble in water, hence floats on water. Vapors heavier than air.
Air & Water Reactions
Highly flammable. Forms peroxides when exposed to air that may initiate spontaneous, exothermic polymerization. Peroxide formation usually proceeds slowly. Slightly soluble in water.
METHYL ACRYLATE ignites readily when exposed to heat, flame or sparks. Offers a dangerous fire and explosion hazard. Reacts vigorously with strong oxidizing materials. Forms peroxides when exposed to air that may initiate spontaneous exothermic polymerization. Peroxide formation usually proceeds slowly. Added inhibitor retards polymerization. If the inhibitor is consumed during long storage, explosive polymerization may occur [MCA Case History No. 2033]. Also subject to strongly exothermic polymerization if heated for prolonged periods or contaminated.
Flammable, dangerous fire and explosion risk. Toxic by inhalation, ingestion, and skin absorption; irritant to skin, eyes and upper respiratory tract irritant; eye damage. Questionable carcinogen.
The liquid is a strong irritant, and prolongedcontact with the eyes or skin may causesevere damage. Inhalation of its vapors cancause lacrimation, irritation of respiratorytract, lethargy, and at high concentrations,convulsions. One-hour exposure to a concen tration of 700–750 ppm in air caused deathto rabbits. The oral toxicity of methyl acry late in animals varied from low to moderate,depending on species, the LD50 values ranging between 250 and 850 mg/kg. The liquidmay be absorbed through the skin, producingmild toxic effects.
Flammable liquid; flash point (closed cup)
-4°C (25°F), (open cup) -3°C (27°F); vapor
pressure 68 torr at 20°C (68°F); vapor density
3.0 (air = 1); the vapor is heavier than air and
can travel a considerable distance to a source
of ignition and flashback; autoignition tem perature not established; fire-extinguishing
agent: dry chemical, CO2, or “alcohol” foam;
use water to keep the fire-exposed containers
cool and to flush or dilute any spill; the vapors
may polymerize and block the vents.
The vapors of methyl acrylate form explo sive mixtures with air, over a relatively wide range; the LEL and UEL values are 2.8 and 25.0% by volume in air, respectively. Methyl acrylate undergoes self-polymerization at 25°C (77°F). The polymerization reaction proceeds with evolution of heat and the increased pressure can cause rupture of closed containers. The reaction rate is accelerated by heat, light, or peroxides. Vigorous to violent reaction may occur when mixed with strong oxidizers (especially nitrates and peroxides) and strong alkalie.
Poison by ingestion and intraperitoneal routes. Moderately toxic by skin contact. Mddly toxic by inhalation. Human systemic effects by inhalation: olfaction effects, eye effects, and respiratory effects. A skin and eye irritant. Mutation data reported. Chronic exposure has produced injury to lungs, liver, and kidneys in experimental animals. Questionable carcinogen. Dangerously flammable when exposed to heat, flame, or oxidzers. Dangerous explosion hazard in the form of vapor when exposed to heat, sparks, or flame. Can react vigorously with oxidzing materials. A storage hazard; it forms peroxides, which may initiate exothermic polymerization. To fight fire, use foam, COa, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.
It is an acute toxin with an LD50 (rats, oral) of 300 mg/kg and a TLV of 10 ppm.
Methyl acrylate is used in production of acrylates, copolymers, barrier resins; and surfactants for shampoos; as a monomer in the manufacture of polymers for plastic films, textiles, paper, and leather coating resins. It is also used as a pesticide intermediate and in pharmaceutical manufacture.
Methyl acrylate was not shown to be carcinogenic in male and female rats in a lifetime inhalation study .
Not listed by ACGIH, California Proposition 65, IARC, NTP, or OSHA.
Photolytic. Polymerizes on standing and is accelerated by heat, light, and peroxides (Windholz
et al., 1983). Methyl acrylate reacts with OH radicals in the atmosphere (296 K) and aqueous
solution at rates of 3.04 x 10-12 and 2.80 x 10-12 cm3/molecule?sec, respectively (Wallington et al.,
Chemical/Physical. Begins to polymerize at 80.2 °C (Weast, 1986). Slowly hydrolyzes in water forming methyl alcohol and acrylic acid (Morrison and Boyd, 1971). Based on a hydrolysis rate constant of 0.0779/M?h at pH 9 at 25 °C, an estimated half-life of 2.8 yr at pH 7 was reported (Roy, 1972). The reported rate constant for the reaction of methacrylonitrile with ozone in the gas phase is 2.91 x 10-18 cm3 mol/sec (Munshi et al., 1989a).
Methyl acrylate is stored in a flammable materials storage room or cabinet below 20°C (68°F), separated from oxidizing substances. It is inhibited with 200 ppm ofhydroquinone monomethyl ether to preventself-polymerization. It is shipped in bottles,cans, drums, or tank cars.
UN1919 Methyl acrylate, stabilized, Hazard Class: 3; Labels: 3-Flammable liquid.
Wash the ester repeatedly with aqueous NaOH until free from inhibitors (such as hydroquinone), then wash it with distilled water, dry (CaCl2) and fractionally distil it under reduced pressure in an all-glass apparatus. Seal it under nitrogen and store it at 0o in the dark. [Bamford & Han J Chem Soc, Faraday Trans 1 78 855 1982, Beilstein 2 IV 1457.]
Methyl acrylate (MA) is moderately toxic to fish (LC50 1.1 - 7.5 mg/l), crustaceans (LC50/EC50 0.31 - 2.6 mg/l) and algae(EC50 6.9 - 15.0 mg/l). In Selenastrum capricornutum, MA is algistatic at a concentration of 19 mg/l.It is of low acute toxicity to bacteria and protozoa.
Forms explosive mixture in air. Incompatible with nitrates, oxidizers, such as peroxides, strong alkalis. Polymerizes easily from heat, light, peroxides; usually contains an inhibitor, such as hydroquinone.
Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal
Methyl acrylate Preparation Products And Raw materials
- 010-82848833- ;010-82848833-
- Methyl acetate
- Tetramethyl Ibandronate
- methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate
- [1-Hydroxy-3-(methylpentylamino)-propylidene]bisphosphonic acid sodium salt
- Trisodium phosphate
- Acryloyl chloride
- b-Alanine, N-methyl-N-pentyl-
- Phosphonic acid, disodium salt
- N-Methyl-N-pentyl-beta-alanine methyl ester
- Ibandronate Impurity 1(Ibandronate EP Impurity B)
- Pamidronic acid
- Ibandronate Impurity 3(Ibandronate EP Impurity C)
- Methyl acrylate
- Octadecyl acrylate