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E9706

Sigma-Aldrich

Ethyl acrylate

contains 10-20 ppm MEHQ as inhibitor, 99%

Sinônimo(s):

Acrylic acid ethyl ester

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About This Item

Fórmula linear:
CH2=CHCOOC2H5
Número CAS:
140-88-5
Peso molecular:
100.12
Beilstein:
773866
Número CE:
205-438-8
Número MDL:
MFCD00009188
Código UNSPSC:
12162002
ID de substância PubChem:
24894702
NACRES:
NA.23

densidade de vapor

3.5 (vs air)

Nível de qualidade

200

pressão de vapor

31 mmHg ( 20 °C)

Ensaio

99%

forma

liquid

temperatura de autoignição

721 °F

contém

10-20 ppm MEHQ as inhibitor

Lim. expl.

12.1 %

índice de refração

n20/D 1.406 (lit.)

pb

99 °C (lit.)

pf

−71 °C (lit.)

densidade

0.918 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CCOC(=O)C=C

InChI

1S/C5H8O2/c1-3-5(6)7-4-2/h3H,1,4H2,2H3

chave InChI

JIGUQPWFLRLWPJ-UHFFFAOYSA-N

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Descrição geral

It is an acrylic monomer. It may be prepared either by reacting acetylene with carbon monoxide and ethyl alcohol in the presence of nickel carbonyl and hydrogen chloride as catalysts, or by catalyzed esterification of acrylic acid with alcohol. It polymerizes readily under the influence of heat, light or other initiators.

Aplicação

Used in the manufacture of a variety of polymers and copolymers. It is also used as an ingredient in latex paints., binders , caulks, lubricating oils, polishes, adhesives, fibers, plastics and other products.

Pictogramas

FlameSkull and crossbones
GHS02,GHS06

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

48.2 °F - closed cup

Ponto de fulgor (°C)

9 °C - closed cup

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
STBK8871
MKCQ6014
STBK3673
STBK3541
MKCN6983

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Methyl acrylate analytical standard

Supelco

76778

Methyl acrylate

Isobutyl acrylate ≥99%, contains 10-20 ppm monomethyl ether hydroquinone as inhibitor

Sigma-Aldrich

436305

Isobutyl acrylate

2-Ethylhexyl acrylate 98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

Sigma-Aldrich

290815

2-Ethylhexyl acrylate

Ácido acrílico anhydrous, contains 200 ppm MEHQ as inhibitor, 99%

Sigma-Aldrich

147230

Ácido acrílico

Butyl acrylate analytical standard

Supelco

06958

Butyl acrylate

Ethyl methacrylate (stabilised) for synthesis

Sigma-Aldrich

8.00579

Ethyl methacrylate

Zahra Bazrafshan et al.
Nanomaterials (Basel, Switzerland), 8(9) (2018-09-13)
A collagen-based copolymer, ASC-g-Poly(methyl methacrylate-co-Ethyl Acrylate), was synthesized in the presence of Graphene Oxide (GO) via an in-situ polymerization. The presence of GO that increased the accessible surface area for initiated collagen chains allowed for an accelerated polymerization with highly
Zahra Bazrafshan et al.
Journal of the mechanical behavior of biomedical materials, 87, 19-29 (2018-07-22)
In this study, Acid Soluble Collagen-g-P(methyl methacrylate-co-ethyl acrylate) (CME) was synthesized to take advantage of the flexibility of the resulted branched polymer chains and the high density of their chain entanglement. The coaxial electrospinning technique was applied to study the
Hui Yang et al.
Polymers, 11(11) (2019-11-21)
A novel elastomer poly(diethyl itaconate-co-butyl acrylate-co-ethyl acrylate-co-glycidyl methacrylate) (PDEBEG) was designed and synthesized by redox emulsion polymerization based on bio-based diethyl itaconate, butyl acrylate, ethyl acrylate, and glycidyl methacrylate. The PDEBEG has a number average molecular weight of more than
Andrea Venturato et al.
Macromolecular bioscience, 16(12), 1864-1872 (2016-10-26)
The development of polymeric materials with cell adhesion abilities requires an understanding of cell-surface interactions which vary with cell type. To investigate the correlation between cell attachment and the nature of the polymer, a series of random and block copolymers
Junliang Wu et al.
Journal of the American Chemical Society, 131(39), 13888-13889 (2009-09-15)
The direct cross-coupling of quinoline-N-oxides with olefin derivatives has been realized using palladium acetate as the catalyst in the absence of external ligand and oxidant to give the corresponding 2-alkenylated quinolines and 1-alkenylated isoquinolines chemo- and regioselectively in 27-95% yield.
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