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About This Item
Linear Formula:
CH2=CHCOOC2H5
CAS Number:
Molecular Weight:
100.12
EC Number:
205-438-8
UNSPSC Code:
12352108
PubChem Substance ID:
Beilstein/REAXYS Number:
773866
MDL number:
Assay:
≥99.0%
Form:
liquid
Grade:
SAJ first grade
Pricing and availability is not currently available.
grade
SAJ first grade
vapor density
3.5 (vs air)
vapor pressure
31 mmHg ( 20 °C)
assay
≥99.0%
form
liquid
autoignition temp.
721 °F
expl. lim.
12.1 %
availability
available only in Japan
refractive index
n20/D 1.406 (lit.)
bp
99 °C (lit.)
mp
−71 °C (lit.)
density
0.918 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)C=C
InChI
1S/C5H8O2/c1-3-5(6)7-4-2/h3H,1,4H2,2H3
InChI key
JIGUQPWFLRLWPJ-UHFFFAOYSA-N
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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
WGK 2
flash_point_f
48.2 °F - closed cup
flash_point_c
9 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Anna E V Hagström et al.
Biotechnology and bioengineering, 102(3), 693-699 (2008-09-30)
An OH-functional polyester has been acrylated via transesterification of ethyl acrylate, catalyzed by Candida antarctica lipase B (CalB) in two different preparations: Novozym 435 and immobilized on Accurel MP1000. The batch process resulted in incomplete acrylation as well as severe
M Monier et al.
Journal of hazardous materials, 176(1-3), 348-355 (2009-12-08)
The graft copolymerization of ethyl acrylate (EA) onto natural wool fibers initiated by potassium persulphate and Mohr's salt redox initiator system in limited aqueous medium was carried out in heterogeneous media. Ester groups of the grafted copolymers were partially converted
M Shahjahan Kabir et al.
The Journal of organic chemistry, 77(1), 300-310 (2011-11-15)
The stereospecific synthesis of aryloxy and amino substituted E- and Z-ethyl-3-acrylates is of interest because of their potential in the polymer industry and in medicinal chemistry. During work on a copper-catalyzed cross-coupling reaction of ethyl (E)- and (Z)-3-iodoacrylates with phenols

