81475
聚(甲基丙烯酸丁酯)
analytical standard, suitable for gel permeation chromatography (GPC), 800,000
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
InChI key
SOGAXMICEFXMKE-UHFFFAOYSA-N
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
mol wt
Mn ~682000, Mp ~772000, Mw ~723000
technique(s)
gel permeation chromatography (GPC): suitable
density
1.07 g/mL at 25 °C (lit.)
Mw/Mn
~1.06
format
neat
Quality Level
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存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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
Monica Bertoldo et al.
Biomacromolecules, 12(2), 388-398 (2011-01-05)
Periodate oxidation and subsequent reductive amination with propargylamine was adopted for the controlled functionalization of amylose with alkyne groups, whereas ATRP polymerization was exploited to obtain end-(α)- or end-(ω)-azide functionalized poly(meth)acrylates to be used as "click" reagents in Cu(I) catalyzed
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