POLY(ISOBUTYL METHACRYLATE)

Product Information

Molecular Formula:
[C8H14O2]n
Description
Firm. water-insensitive. polymer.
[η] = 0.60
Synonyms
ISOBUTYL METHACRYLATE POLYMER; ISO-BUTYL METHACRYLATE RESIN; METHACRYLIC ACID ISOBUTYL ESTER POLYMER; 2-Propenoicacid,2-methyl-,2-methylpropylester,homopolymer; Isobutylmethacrylate,homopolymer; Isobutylmethacrylatehomopolymer; POLY(ISOBUTYL METHACRYLATE); POLY
IUPAC Name
2-methylpropyl 2-methylprop-2-enoate
Canonical SMILES
CC(C)COC(=O)C(=C)C
InChI
InChI=1S/C8H14O2/c1-6(2)5-10-8(9)7(3)4/h6H,3,5H2,1-2,4H3
InChI Key
RUMACXVDVNRZJZ-UHFFFAOYSA-N
Boiling Point
160°C at 760mmHg
Flash Point
120 °F
Purity
high molecular weight
Density
1.09 g/mL at 25 °C
Solubility
Insoluble (<1mg/ml)
Appearance
Liquid
Application
Used as a monomer for acrylic resins, in hydrogel contact lenses, and as a water repellant for concrete.
Storage
Store at room temperature
Refractive Index
n20/D 1.477
Tg
53°
LogP
log Kow = 2.66
Vapor Pressure
3.63 [mmHg]
Henry's Law Constant
5.2X10-4 atm-cu m/mole at 25 °C (est)
Decomposition
When heated to decomposition it emits acrid smoke and fumes.

Safety Information

Hazards
Harmless-use normal precautions
Handling
Exercise normal care

Computed Properties

XLogP3
2.7
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
4
Exact Mass
142.099379685 g/mol
Monoisotopic Mass
142.099379685 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
136
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2021123196-A1 Seeded resin-stabilized high-solids emulsion polymers 2019-12-20
WO-2021123309-A1 Composition comprising a dispersion of polymer particles in a non-aqueous medium, a cationic polymer and an anionic polymer 2019-12-20
WO-2021124043-A1 Adhesive article comprising polymer and polymerizable cyclic olefins, adhesive compositions and methods 2019-12-20
WO-2021125292-A1 Methacrylic copolymer, production method therefor, methacrylic copolymer composition, and molded body 2019-12-20
WO-2021126780-A1 Combination of crosslinkers to improve coating properties 2019-12-20
WO-2021121795-A1 Polyacrylate-based graft copolymer 2019-12-19
WO-2021123116-A1 Adhesive photoprotective compounds and uses thereof 2019-12-19
US-2021189034-A1 Polymer particles, rubber composition and tire 2019-12-18
WO-2021122692-A1 Textile coated with malodor reducing polymers 2019-12-18
WO-2021123691-A1 Composition comprising a hemiperoxyacetal, method for polymerizing same, use thereof, and composition material obtained upon polymerization of the composition 2019-12-18

Literatures

PMID Publication Date Title Journal
22489207 2012-01-01 Separation of poly(styrene-block-t-butyl methacrylate) copolymers by various liquid chromatography techniques TheScientificWorldJournal
21711747 2011-03-22 Temperature- and thickness-dependent elastic moduli of polymer thin films Nanoscale research letters
20650509 2010-10-01 Cytotoxicity of monomers, plasticizer and degradation by-products released from dental hard chairside reline resins Dental materials : official publication of the Academy of Dental Materials
20121228 2010-02-23 Direct patterning of intrinsically electron beam sensitive polymer brushes ACS nano
20157935 2009-11-01 Effect of microwave postpolymerization treatment and of storage time in water on the cytotoxicity of denture base and reline acrylic resins Quintessence international (Berlin, Germany : 1985)
19366199 2009-05-19 Fibrinogen adsorption and conformational change on model polymers: novel aspects of mutual molecular rearrangement Langmuir : the ACS journal of surfaces and colloids
17635028 2008-03-01 Effect of molecular mobility of polymeric implants on soft tissue reactions: an in vivo study in rats Journal of biomedical materials research. Part A
17880031 2007-11-01 Single-step preparation and characterization of polymeric monolith for pressurized capillary electrochromatography of typical homologs Journal of separation science
17242998 2007-06-01 Fabrication of hydroxyapatite-poly(epsilon-caprolactone) scaffolds by a combination of the extrusion and bi-axial lamination processes Journal of materials science. Materials in medicine
16875795 2007-01-04 Rapid separation and determination of structurally related anthraquinones in Rhubarb by pressurized capillary electrochromatography Journal of pharmaceutical and biomedical analysis
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International: 1-631-504-6093
  • US & Canada (Toll free): 1-844-BOC(262)-0123
  • 45-16 Ramsey Road, Shirley, NY 11967, USA
  • Email: info@bocsci.com
  • Fax: 1-631-614-7828
UK
  • 44-20-3286-1088
  • 85 Great Portland Street, London, W1W 7LT
  • Email: info@bocsci.com
Copyright © 2025 BOC Sciences. All rights reserved.
Top
0
Inquiry Basket

No data available, please add!

Delete selectedGo to checkout

We use cookies to understand how you use our site and to improve the overall user experience. This includes personalizing content and advertising. Read our Privacy Policy

Accept Cookies
x