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181528

Sigma-Aldrich

Poly(butylmethacrylat)

inherent viscosity 0.470-0.560 dL/g 

Synonym(e):

PBMA

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About This Item

CAS-Nummer:
9003-63-8
EG-Nummer:
202-615-1
MDL-Nummer:
MFCD00084402
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24850940
NACRES:
NA.23

Form

powder

Mol-Gew.

200000

Brechungsindex

n20/D 1.483

Inhärente Viskosität

0.470-0.560 dL/g

Dichte

1.07 g/mL at 25 °C (lit.)

SMILES String

CCCCOC(=O)C(C)=C

InChI

1S/C8H14O2/c1-4-5-6-10-8(9)7(2)3/h2,4-6H2,1,3H3

InChIKey

SOGAXMICEFXMKE-UHFFFAOYSA-N

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Allgemeine Beschreibung

Poly(butyl methacrylate) is a highly biocompatible polymer widely usedin drug delivery coatings.

Anwendung

Poly(butyl methacrylate) has been used as a matrix to fabricate NO-releasing polymer films by solvent casting approach.

It can be used to prepare thermoresponsive microfibers with excellent mechanical properties. PBMA-containing microfibers can be used as temperature-modulated cell separation materials.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H317

Gefahreneinstufungen

Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Poly(methylmethacrylat-co-ethylacrylat) ethyl acrylate <5 wt. %, average Mn ~39,500 by GPC, average Mw ~101,000 by GPC, powder

Sigma-Aldrich

182249

Poly(methylmethacrylat-co-ethylacrylat)

Temperature dependent photoluminescence down to 4.2 K in EuTFC.
Haugen and Johansen TH
Journal of Luminescence, 128(9), 1479-1483 (2008)
Birthe V Nielsen et al.
Biomedical materials (Bristol, England), 6(1), 015003-015003 (2011-01-06)
Towards the evaluation of non-permanent dental coatings for their capacity to impart dental-care benefits, thin films of a homologous series of comb-like poly(alkyl methacrylate)s (ethyl to octadecyl) have been deposited, from aqueous latex formulations, onto dentally relevant substrates. AFM studies
Jingguo Shen et al.
Journal of the American Chemical Society, 130(33), 10866-10867 (2008-07-24)
We demonstrate the self-assembly through fluorophilic interactions of a blend of perfluorocarbon (RF) end-functionalized polystyrene and the corresponding RF-polybutylmethacrylate into optically transparent materials that retain domain characteristics typical of the component polymers but show well-defined lamellar nanostructured morphologies that qualitatively
Mariano Licciardi et al.
International journal of pharmaceutics, 433(1-2), 16-24 (2012-05-12)
Polymeric microparticles encapsulating two model hydrophobic drugs, beclomethasone dipropionate (BDP) and flutamide (FLU) were prepared by using the high pressure homogenization-solvent evaporation method starting from a oil-in-water emulsion. For the preparation of polymeric microparticles a α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA) graft copolymer with
Masamichi Nakayama et al.
Macromolecular bioscience, 12(6), 751-760 (2012-04-21)
Thermoresponsive surfaces are prepared via a spin-coating method with a block copolymer consisting of poly(N-isopropylacrylamide) (PIPAAm) and poly(butyl methacrylate) (PBMA) on polystyrene surfaces. The PBMA block suppresses the removal of deposited PIPAAm-based polymers from the surface. The polymer coating affects
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