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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)
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
Petr Kubán et al.
Journal of separation science, 31(15), 2745-2753 (2008-07-31)
We describe ion chromatography (IC) on open tubular cation exchange columns with a controllable capacity multilayered stationary phase architecture. The columns of relatively large bore (75 microm id) are fabricated by coating fused-silica capillaries with multiple layers of poly(butadiene-maleic acid)
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
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