181528
Poly(butyl methacrylate)
Synonym(s):
PBMA
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
CAS Number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
202-615-1
MDL number:
form
powder
Quality Level
mol wt
200000
refractive index
n20/D 1.483
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
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.
It can be used to prepare thermoresponsive microfibers with excellent mechanical properties. PBMA-containing microfibers can be used as temperature-modulated cell separation materials.
Still not finding the right product?
Explore all of our products under Poly(butyl methacrylate)
signalword
Warning
hcodes
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)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Self-assembled monolayers (SAMs) have diverse applications; article compares benefits of alkylthiolates on gold SAM systems.
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 181528-5G | 04061838755322 |
| 181528-250G | 04061838755315 |