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Merck
CN

181528

Poly(butyl methacrylate)

Synonym(s):

PBMA

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About This Item

CAS Number:
9003-63-8
NACRES:
NA.23
PubChem Substance ID:
24850940
UNSPSC Code:
12162002
EC Number:
202-615-1
MDL number:
MFCD00084402

Key Documents

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InChI key

SOGAXMICEFXMKE-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCOC(=O)C(C)=C

form

powder

mol wt

200000

refractive index

n20/D 1.483

density

1.07 g/mL at 25 °C (lit.)

Quality Level

100

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General description

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

Application

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX0732
MKCL4348
MKCK8008
MKCJ4721
MKCH9103

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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
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
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
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
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