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19-2380

Sigma-Aldrich

Methyl acrylate

SAJ first grade, ≥99.0%

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About This Item

Linear Formula:
CH2=CHCOOCH3
CAS Number:
96-33-3
Molecular Weight:
86.09
Beilstein/REAXYS Number:
605396
EC Number:
202-500-6
MDL number:
MFCD00008627
UNSPSC Code:
12352108
PubChem Substance ID:
329751696
grade:
SAJ first grade
assay:
≥99.0%
bp:
80 °C (lit.)
vapor pressure:
67.5 mmHg ( 20 °C)
Pricing and availability is not currently available.

grade

SAJ first grade

vapor density

3 (vs air)

vapor pressure

67.5 mmHg ( 20 °C)

assay

≥99.0%

form

liquid

autoignition temp.

874 °F

expl. lim.

14.5 %

availability

available only in Japan

dilution

(for analytical testing)

refractive index

n20/D 1.402 (lit.)

bp

80 °C (lit.)

mp

−75 °C (lit.)

density

0.956 g/mL at 25 °C (lit.)

SMILES string

COC(=O)C=C

InChI

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

InChI key

BAPJBEWLBFYGME-UHFFFAOYSA-N

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pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

27.0 °F - closed cup

flash_point_c

-2.8 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
A5141
A8761
A5638
A3547
A1481

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Jens Voepel et al.
Biomacromolecules, 12(1), 253-259 (2010-12-21)
A multifunctional macroinitiator for single-electron-transfer mediated living radical polymerization (SET-LRP) was designed from acetylated galactoglucomannan (AcGGM) by α-bromoisobutyric acid functionalization of the anomeric hydroxyl groups on the heteropolysaccharide backbone. This macroinitiator, with a degree of substitution of 0.15, was used
Xin Liu et al.
Journal of hazardous materials, 175(1-3), 1014-1021 (2009-11-27)
Porous acrylonitrile (AN)/methyl acrylate (MA) copolymer beads were prepared by suspended emulsion polymerization. The cyano groups in AN/MA copolymer beads were converted to amidoxime (AO) groups by reaction with hydroxylamine hydrochloride (NH(2)OH.HCl) to remove metal ions in aqueous solution. The
Nicky Chan et al.
Macromolecular rapid communications, 32(7), 604-609 (2011-03-26)
The use of copper tubing as both the reactor and as a catalyst source is demonstrated for continuous controlled radical polymerization of methyl acrylate at ambient temperature and at low solvent content of 30%. The high surface area provided by
Transformation of nickelalactones to methyl acrylate: on the way to a catalytic conversion of carbon dioxide.
S Y Tina Lee et al.
ChemSusChem, 4(9), 1275-1279 (2011-09-17)
Boris Neuwald et al.
Journal of the American Chemical Society, 135(3), 1026-1036 (2012-12-22)
Various phosphinesulfonato ligands and the corresponding palladium complexes [{((P^O)PdMeCl)-μ-M}(n)] ([{((X)1-Cl)-μ-M}(n)], (P^O) = κ(2)-P,O-Ar(2)PC(6)H(4)SO(2)O) with symmetric (Ar = 2-MeOC(6)H(4), 2-CF(3)C(6)H(4), 2,6-(MeO)(2)C(6)H(3), 2,6-(iPrO)(2)C(6)H(3), 2-(2',6'-(MeO)(2)C(6)H(3))C(6)H(4)) and asymmetric substituted phosphorus atoms (Ar(1) = 2,6-(MeO)(2)C(6)H(3), Ar(2) = 2'-(2,6-(MeO)(2)C(6)H(3))C(6)H(4); Ar(1) = 2,6-(MeO)(2)C(6)H(3), Ar(2) = 2-cHexOC(6)H(4)) were
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