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17348

Sigma-Aldrich

2-Hydroxyethyl methacrylate

embedding medium (for microscopy)

Sinônimo(s):

1,2-Ethanediol mono(2-methylpropenoate), Glycol methacrylate, HEMA

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About This Item

Fórmula linear:
CH2=C(CH3)COOCH2CH2OH
Número CAS:
868-77-9
Peso molecular:
130.14
Beilstein:
1071583
Número CE:
212-782-2
Número MDL:
MFCD00002863
Código UNSPSC:
12162002
ID de substância PubChem:
57647639
NACRES:
NA.25

grau

embedding medium (for microscopy)

densidade de vapor

5 (vs air)

pressão de vapor

0.01 mmHg ( 25 °C)

Ensaio

≥99%

forma

liquid

contém

~0.001% hydroquinone monomethyl ether as stabilizer

Impurezas

<250 mg/kg free acid (as methycrylic acid) (T)

índice de refração

n20/D 1.453 (lit.)
n20/D 1.453

pb

67 °C/3.5 mmHg (lit.)

densidade

1.071 g/mL at 20 °C
1.073 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CC(=C)C(=O)OCCO

InChI

1S/C6H10O3/c1-5(2)6(8)9-4-3-7/h7H,1,3-4H2,2H3

chave InChI

WOBHKFSMXKNTIM-UHFFFAOYSA-N

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Aplicação

2-Hydroxyethyl methacrylate has been used in a study to describe a novel methodology for grafting polymers via radical photopolymerization initiated on gold surfaces by aryl layers from diazonium salt precursors. 2-Hydroxyethyl methacrylate has also been used in a study to provide insight into the induction of apoptosis and the differential expression of antioxidant enzymes depending on the availability of glutathione.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H317,H319

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

222.8 °F - closed cup

Ponto de fulgor (°C)

106 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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Sarra Gam-Derouich et al.
Langmuir : the ACS journal of surfaces and colloids, 28(21), 8035-8045 (2012-05-03)
In this paper we describe a novel methodology for grafting polymers via radical photopolymerization initiated on gold surfaces by aryl layers from diazonium salt precursors. The parent 4-(dimethylamino)benzenediazonium salt was electroreduced on a gold surface to provide 4-(dimethylamino)phenyl (DMA) hydrogen
Stephanie Krifka et al.
Biomaterials, 33(21), 5177-5186 (2012-04-27)
Resin monomers like 2-hydroxyethyl methacrylate (HEMA) disturb cell functions including responses of the innate immune system, mineralization and differentiation, or induce cell death via apoptosis. These phenomena are associated with oxidative stress and a reduction in the concentration of the
Brendan P Purcell et al.
Biomaterials, 33(31), 7849-7857 (2012-07-28)
Poor cell engraftment in the myocardium is a limiting factor towards the use of bone marrow derived cells (BMCs) to treat myocardial infarction (MI). In order to enhance the engraftment of circulating BMCs in the myocardium following MI, we have
Duncan Chege et al.
Journal of acquired immune deficiency syndromes (1999), 65(5), 517-525 (2013-11-22)
To evaluate if systemic murine malarial infection enhances HIV susceptibility through parasite-induced mucosal immune alterations at sites of HIV sexual exposure. Malaria and HIV have a high degree of geographical overlap and interact substantially within coinfected individuals. We used a
M Bourbia et al.
Journal of dental research, 92(11), 989-994 (2013-09-13)
A major reason for dental resin composite restoration replacement is related to secondary caries promoted by acid production from bacteria including Streptococcus mutans (S. mutans). We hypothesized that S. mutans has esterase activities that degrade dental resin composites and adhesives.
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