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292818

Sigma-Aldrich

2-Hydroxyethyl acrylate

96%, contains 200-650 ppm monomethyl ether hydroquinone as inhibitor

Synonyme(s) :

Ethylene glycol monoacrylate

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About This Item

Formule linéaire :
CH2=CHCOOCH2CH2OH
Numéro CAS:
818-61-1
Poids moléculaire :
116.12
Numéro Beilstein :
969853
Numéro CE :
212-454-9
Numéro MDL:
MFCD00002865
Code UNSPSC :
12162002
ID de substance PubChem :
24857612
Nomenclature NACRES :
NA.23

Densité de vapeur

>1 (vs air)

Niveau de qualité

100

Pression de vapeur

<0.1 mmHg ( 20 °C)

Pureté

96%

Forme

solid

Contient

200-650 ppm monomethyl ether hydroquinone as inhibitor

Indice de réfraction

n20/D 1.45 (lit.)

Point d'ébullition

90-92 °C/12 mmHg (lit.)

Densité

1.011 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

OCCOC(=O)C=C

InChI

1S/C5H8O3/c1-2-5(7)8-4-3-6/h2,6H,1,3-4H2

Clé InChI

OMIGHNLMNHATMP-UHFFFAOYSA-N

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Description générale

2-Hydroxyethyl acrylate (HEA) is a monomer that is widely used in the field of material synthesis for the production of various types of polymers, such as hydrogels, coatings, adhesives, and thermosets. Its versatility lies in its ability to copolymerize with a variety of monomers, resulting in a wide range of polymer properties and applications. Its main use is in the production of hydrogels, which are highly absorbent and can be used in wound dressings, contact lenses, drug delivery systems, and other biomedical applications. Additionally, 2-hydroxyethyl acrylate-based coatings and adhesives are used in various surface modification and bonding applications, owing to their excellent adhesion, flexibility, and chemical resistance properties.

Application

Porous hydrogels can be prepared by copolymerization of 2-hydroxyethyl acrylate and a cross linking agent. 2-hydroxyethyl acrylate may be used in the synthesis of amphilic block copolymers by nitroxide mediated living radical polymeration. Also, it may be used to prepare tuned poly(hydroxyethyl acrylate) by atom transfer radical polymerization.

Pictogrammes

Skull and crossbonesCorrosionEnvironment
GHS06,GHS05,GHS09

Mention d'avertissement

Danger

Mentions de danger

H302,H311,H314,H317,H410

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

213.8 °F - closed cup

Point d'éclair (°C)

101 °C - closed cup

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
STBK7418
STBK3755
STBK1308
STBJ3891
STBJ0983

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

J M Boothby et al.
Soft matter, 13(24), 4349-4356 (2017-05-04)
Materials that change shape are attractive candidates to replace traditional actuators for applications with power or size restrictions. In this work, we design a polymeric bilayer that changes shape in response to both heat and water by the incorporation of
Tugba Ozdemir et al.
ACS biomaterials science & engineering, 2(12), 2217-2230 (2016-12-19)
Current treatments for chronic xerostomia, or "dry mouth", do not offer long-term therapeutic benefits for head and neck cancer survivors previously treated with curative radiation. Towards the goal of creating tissue-engineered constructs for the restoration of salivary gland functions, we
Atom transfer radical polymerization of tert-butyl acrylate and preparation of block copolymers.
Davis KA and Matyjaszewski K
Macromolecules, 33(11), 4039-4047 (2000)
J C Tiller et al.
Journal of controlled release : official journal of the Controlled Release Society, 103(2), 355-367 (2005-03-15)
Bitelechelic polydimethylsiloxanes (PDMS) and 2-hydroxyethylacrylate (HEA)/acrylic acid(AA) were photopolymerized to give nanophase separated amphiphilic 20-mum-thin coatings covalently attached to glass. The coatings quickly take up the antimicrobial surfactant cetyltrimethylammonium chloride (CTAC). After a 30 min loading period the release of
Richard Hoogenboom et al.
Macromolecular rapid communications, 30(23), 2042-2048 (2009-12-01)
Poly(2-hydroxyethyl acrylate) (PHEA) is an interesting biomaterial with similar biocompatibility as the widespread used poly(2-hydroxyethyl methacrylate). Poly(2-hydroxypropyl acrylate) (PHPA) is a less frequently studied polymer that exhibits thermoresponsive behavior in water. Therefore, copolymers of HEA and HPA are interesting thermoresponsive
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