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09-0750

Sigma-Aldrich

Ethyl acrylate

SAJ first grade, ≥99.0%

Sinónimos:

Acrylic acid ethyl ester

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About This Item

Fórmula lineal:
CH2=CHCOOC2H5
Número de CAS:
140-88-5
Peso molecular:
100.12
Beilstein/REAXYS Number:
773866
EC Number:
205-438-8
MDL number:
MFCD00009188
UNSPSC Code:
12352108
PubChem Substance ID:
329748675

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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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

48.2 °F - closed cup

flash_point_c

9 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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.
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
Aaron Mark Drucker et al.
Dermatitis : contact, atopic, occupational, drug, 22(2), 98-101 (2011-04-21)
Acrylates are present in a wide variety of products and cause occupational and non-occupational allergic contact dermatitis. There is no clear guidance from the literature as to which allergens should be used for patch-test screening for acrylates. To characterize patients
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
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