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Key Documents

182079

Sigma-Aldrich

Poly(2-ethylhexyl methacrylate) solution

average Mw ~100,000 by GPC, in toluene

Synonym(s):

2-Ethylhexyl methacrylate homopolymer, Poly(ethylhexyl methacrylate)

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About This Item

Linear Formula:
(C12H22O2)n
CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

1.2 (37 °C, vs air)

form

liquid

mol wt

average Mw ~100,000 by GPC

concentration

in toluene

weight

Unit weight does not include weight of solvent.

transition temp

Tg −10 °C

density

0.908 g/mL at 25 °C

SMILES string

CCCCC(CC)COC(=O)C(C)=C

InChI

1S/C12H22O2/c1-5-7-8-11(6-2)9-14-12(13)10(3)4/h11H,3,5-9H2,1-2,4H3

InChI key

WDQMWEYDKDCEHT-UHFFFAOYSA-N

General description

PEHMA exhibits biomimetic properties. It finds potential application as a flexible hydrogel for ophthalmologic applications.

Application

Poly(2-ethylhexyl methacrylate) (PEHMA) may be used to synthesize binary polymeric blends with poly(butyl methacrylate). PEHMA may be utilized in the preparation of PEHMA /carbon black composites for gas sensing. PHEMA-antioxidant conjugate (Quercetin (Q) ) may be prepared for ophthalmologic uses.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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An energy tranfer study of the interface thickness in blends of poly (butyl methacrylate) and poly (2-ethylhexyl methacrylate).
Farinha J P S, et al.
Macromolecules, 33(16), 5863-5873 (2000)
Poly (2-hydroxyethyl methacrylate)-quercetin Conjugate as Biomaterial in Ophthalmology: An ?ab initio? Study.
Curcio M, et al.
Journal of Functional Biomaterials, 2(1), 1-17 (2011)
Carbon black filled poly (2-ethylhexyl methacrylate) as a candidate for gas sensing material.
Dong X M, et al.
Journal of Materials Science Letters, 22(15), 1057-1059 (2003)

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Self-assembled monolayers (SAMs) have attracted enormous interest for a wide variety of applications in micro- and nano-technology. In this article, we compare the benefits of three different classes of SAM systems (alkylthiolates on gold).

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