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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)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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)
Kadhiravan Shanmuganathan et al.
ACS applied materials & interfaces, 2(1), 165-174 (2010-03-23)
A new series of biomimetic stimuli-responsive nanocomposites, which change their mechanical properties upon exposure to physiological conditions, was prepared and investigated. The materials were produced by introducing percolating networks of cellulose nanofibers or "whiskers" derived from tunicates into poly(vinyl acetate)
Zhen Jiao et al.
Pharmaceutical development and technology, 17(2), 164-169 (2010-10-28)
Amphiphilic block copolymer micelle is one of the most important drug delivery systems to improve the water-solubility of lipophilic drugs. Blank micelles were prepared by solvent evaporation method in order to choose the suitable solvents for PBMA-b-PMPC (poly(n-butyl methacrylate)-b-poly(2-methacryloyloxyethyl phosphorylcholine))
Joanna Pietrasik et al.
Macromolecular rapid communications, 32(3), 295-301 (2011-03-25)
Hybrid nanoparticles with a silica core and grafted poly(methyl methacrylate) (PMMA) or poly(n-butyl methacrylate) (PBMA) chains were prepared via activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP) at room temperature under high pressure. Due to enhanced
Wei Li et al.
International journal of nanomedicine, 7, 4661-4677 (2012-09-15)
The main obstacles for cationic polyplexes in gene delivery are in vivo instability and low solid-tumor accumulation. Safe vectors with high transfection efficiency and in vivo tumor accumulation are therefore highly desirable. In this study, the amphiphilic block copolymer poly(n-butyl
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Artikel

Micro and Nanometer Scale Photopatterning of Self-Assembled Monolayers

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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