Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

181528

Sigma-Aldrich

Poly(butyl methacrylate)

inherent viscosity 0.470-0.560 dL/g 

Synonym(s):

PBMA

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

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

form

powder

Quality Level

100

mol wt

200000

refractive index

n20/D 1.483

inherent viscosity

0.470-0.560 dL/g

density

1.07 g/mL at 25 °C (lit.)

SMILES string

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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Warning

Hazard Statements

H317

Hazard Classifications

Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCL4348
MKCK8008
MKCJ4721
MKCH9103
MKCH8978

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Poly(methyl methacrylate-co-ethyl acrylate) ethyl acrylate <5 wt. %, average Mn ~39,500 by GPC, average Mw ~101,000 by GPC, powder

Sigma-Aldrich

182249

Poly(methyl methacrylate-co-ethyl acrylate)

Temperature dependent photoluminescence down to 4.2 K in EuTFC.
Haugen and Johansen TH
Journal of Luminescence, 128(9), 1479-1483 (2008)
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)
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
View All Related Papers

Articles

Photopatterning Self-Assembled Monolayers

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

Photopatterning Self-Assembled Monolayers

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

Photopatterning Self-Assembled Monolayers

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

Photopatterning Self-Assembled Monolayers

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service