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76130

Supelco

Ethyl acrylate

analytical standard

Sinonimo/i:

Acrylic acid ethyl ester

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5 ML
111,00 €

111,00 €

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5 ML
111,00 €

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:
85151701
ID PubChem:
329766922
NACRES:
NA.24

111,00 €

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Grado

analytical standard

Livello qualitativo

100

Densità del vapore

3.5 (vs air)

Tensione di vapore

31 mmHg ( 20 °C)

Saggio

≥99.5% (GC)

Temp. autoaccensione

721 °F

Durata

limited shelf life, expiry date on the label

contiene

~0.002% hydroquinone monomethyl ether as stabilizer

Limite di esplosione

12.1 %

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.406 (lit.)
n20/D 1.406

P. ebollizione

99 °C (lit.)

Punto di fusione

−71 °C (lit.)

Densità

0.921 g/mL at 20 °C
0.918 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
petroleum

Formato

neat

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

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Applicazioni

Ethyl acrylate can undergo anionic polymerization upon initiation by tetrabutylammonium azide in the presence of alkylaluminum bisphenoxides in toluene to yield azide-end poly(ethyl acrylate) (PEA).[1]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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
BCCL3948
BCCH5811
BCCF7422
BCCC8184
BCBZ8590

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Supelco

43348

Farnesol

Anionic polymerization of ethyl acrylate initiated by tetrabutylammonium azide: direct synthesis of end-clickable polyacrylate
Kataoka Y, et al.
Polym. Chem. (2017)
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
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
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
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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