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E9706

Sigma-Aldrich

Ethyl acrylate

contains 10-20 ppm MEHQ as inhibitor, 99%

Sinonimo/i:

Acrylic acid ethyl ester

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About This Item

Formula condensata:
CH2=CHCOOC2H5
Numero CAS:
140-88-5
Peso molecolare:
100.12
Beilstein:
773866
Numero CE:
205-438-8
Numero MDL:
MFCD00009188
Codice UNSPSC:
12162002
ID PubChem:
24894702
NACRES:
NA.23

Densità del vapore

3.5 (vs air)

Livello qualitativo

200

Tensione di vapore

31 mmHg ( 20 °C)

Saggio

99%

Forma fisica

liquid

Temp. autoaccensione

721 °F

contiene

10-20 ppm MEHQ as inhibitor

Limite di esplosione

12.1 %

Indice di rifrazione

n20/D 1.406 (lit.)

P. eboll.

99 °C (lit.)

Punto di fusione

−71 °C (lit.)

Densità

0.918 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

CCOC(=O)C=C

InChI

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

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Descrizione generale

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.

Applicazioni

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.

Pittogrammi

FlameSkull and crossbones
GHS02,GHS06

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

48.2 °F - closed cup

Punto d’infiammabilità (°C)

9 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (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

Acido acrilico anhydrous, contains 200 ppm MEHQ as inhibitor, 99%

Sigma-Aldrich

147230

Acido acrilico

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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