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Merck
CN

181528

聚(甲基丙烯酸丁酯)

别名:

PBMA

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化学文摘社编号:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
202-615-1
MDL number:
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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

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General description

聚甲基丙烯酸丁酯是一种高度生物相容性聚合物,广泛应用于药物输送涂层。

Application

聚甲基丙烯酸丁酯可作为基质用于溶剂浇铸方法进行NO释放聚合膜的制造。

它也可用于制备具有良好的机械性质的热响应性微纤维。含PBMA微纤维可用作温度调控型电池隔膜材料。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Sens. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

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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)
Nagu Daraboina et al.
Ultrasonics sonochemistry, 16(2), 273-279 (2008-10-14)
The influence of the alkyl group substituents on the ultrasonic degradation of poly (alkyl methacrylate)s, namely poly (methyl methacrylate) (PMMA), poly (ethyl methacrylate) (PEMA) and poly (butyl methacrylate) (PBMA) was studied. The rate coefficient increased with an increase in the
Shigeto Fujishita et al.
Colloids and surfaces. B, Biointerfaces, 74(1), 45-50 (2009-07-18)
Telechelic poly(n-butyl methacrylate)s (PBMAs) with various end groups were prepared using nonionic, anionic, cationic or zwitterionic azo-type radical initiators and cell adhesion onto the surfaces of the polymers was investigated. The tendency for cell adhesion to the polymers differed with
Boris Obermeier et al.
Biomacromolecules, 12(2), 425-431 (2011-01-05)
Partially quarternized poly(methacrylate) terpolymers (Q-BBMCs) have been synthesized, based on the basic butylated methacrylate copolymer (BBMC/EUDRAGIT E), an excipient approved by the Food and Drug Administration (FDA) and to date mainly applied for tablet coatings. Via straightforward polymer modification reactions
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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Self-assembled monolayers (SAMs) have diverse applications; article compares benefits of alkylthiolates on gold SAM systems.

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