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Merck
CN

181528

Sigma-Aldrich

聚(甲基丙烯酸丁酯)

别名:

PBMA

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化学文摘社编号:
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:
NACRES:
NA.23
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表单

powder

分子量

200000

折射率

n20/D 1.483

密度

1.07 g/mL at 25 °C (lit.)

SMILES字符串

CCCCOC(=O)C(C)=C

InChI

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

InChI key

SOGAXMICEFXMKE-UHFFFAOYSA-N

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一般描述

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。

应用

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。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
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
Monique van Hulst et al.
Journal of separation science, 33(10), 1414-1420 (2010-03-24)
A comprehensive 2-D separation method was developed for the characterization of methacrylate copolymers. In both dimensions conditions were employed that give a critical separation for the homopolymer of one of the monomers in the copolymer, and exclusion behaviour for the
Bolong Yao et al.
Bioprocess and biosystems engineering, 33(4), 457-463 (2009-07-07)
Sodium alginate was hydrophobically modified by coupling of polybutyl methacrylate onto the alginate. The polybutyl methacrylate was previously prepared through polymerization of butyl methacrylate in the presence of 2-amino-ethanethiol as a chain transfer agent. The structure of the product was

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Self-assembled monolayers (SAMs) have diverse applications; article compares benefits of alkylthiolates on gold SAM systems.

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