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Merck

E9706

Ethyl acrylate

contains 10-20 ppm MEHQ as inhibitor, 99%

Sinónimos:

Acrylic acid ethyl ester

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Fórmula lineal:
CH2=CHCOOC2H5
Número CAS:
140-88-5
Peso molecular:
100.12
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24894702
EC Number:
205-438-8
Beilstein/REAXYS Number:
773866
MDL number:
MFCD00009188

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Nombre del producto

Ethyl acrylate, contains 10-20 ppm MEHQ as inhibitor, 99%

form

liquid

InChI

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

InChI key

JIGUQPWFLRLWPJ-UHFFFAOYSA-N

SMILES string

CCOC(=O)C=C

vapor density

3.5 (vs air)

vapor pressure

31 mmHg ( 20 °C)

assay

99%

autoignition temp.

721 °F

contains

10-20 ppm MEHQ as inhibitor

expl. lim.

12.1 %

refractive index

n20/D 1.406 (lit.)

bp

99 °C (lit.)

mp

−71 °C (lit.)

density

0.918 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

200

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Application

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.

General description

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.

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

Clase de almacenamiento

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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Certificados de análisis (COA)

Lot/Batch Number
SDBB5111
SDBB5110
SDBB0748
SDBB1927
SDBB1928

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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
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
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
Jiaan Shao et al.
Organic letters, 14(21), 5452-5455 (2012-10-26)
Palladium-catalyzed C-H functionalization using guanidine as the directing group was achieved under mild reaction conditions. Various guanidine derivatives were produced in moderate to good yields by using simple unactivated arenes or ethyl acrylate as the source of arylation or olefination
Marilene S Oliveira et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 10(10), 1546-1555 (2011-07-08)
Singlet molecular oxygen O(2)((1)Δ(g)) is a potent oxidant that can react with different biomolecules, including DNA, lipids and proteins. Many polycyclic aromatic hydrocarbons have been studied as O(2)((1)Δ(g)) chemical traps. Nevertheless, a suitable modification in the polycyclic aromatic ring must
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