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235865

Sigma-Aldrich

Butyl methacrylate

99%, contains monomethyl ether hydroquinone as inhibitor

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About This Item

Formule linéaire :
CH2=C(CH3)COO(CH2)3CH3
Numéro CAS:
97-88-1
Poids moléculaire :
142.20
Numéro Beilstein :
773960
Numéro CE :
202-615-1
Numéro MDL:
MFCD00009444
Code UNSPSC :
12162002
ID de substance PubChem :
24854121
Nomenclature NACRES :
NA.23

Densité de vapeur

4.91 (15 °C, vs air)

Pression de vapeur

2 mmHg ( 20 °C)

Pureté

99%

Forme

liquid

Température d'inflammation spontanée

562 °F

Contient

monomethyl ether hydroquinone as inhibitor

Limite d'explosivité

2-8 %

Indice de réfraction

n20/D 1.423 (lit.)

Point d'ébullition

162-165 °C (lit.)

Densité

0.894 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

CCCCOC(=O)C(C)=C

InChI

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

Clé InChI

SOGAXMICEFXMKE-UHFFFAOYSA-N

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Description générale

Butyl methacrylate is an organic compound that belongs to the class of methacrylate esters and is commonly used in the production of various polymer materials. It can be copolymerized with other monomers to synthesize copolymers with tailored properties. The resulting copolymers find use in numerous fields, including automotive coatings, textiles, adhesives, contact lenses, and dental resins.

Application

Butyl methacrylate (BMA) can be used as:
  • A Monomer to synthesize waterborne butyl methacrylate (co)polymers latexes via emulsion polymerization for the development of coating materials for slow release-fertilizers.
  • A matrix polymer in the preparation of LDH/poly (butyl methacrylate) nanocomposites, which can improve the mechanical properties and thermal stability of the resulting nanocomposites.
  • A monomer to synthesize styrene and butyl methacrylate copolymers for use in leather finishing. Increasing the BMA content of the copolymer increases the water resistance and decreases the water vapor permeability of the leather.
  • A monomer for the preparation of monolithic columns on microfluidic chips. These columns can be used for a wide range of applications, such as the separation and analysis of complex mixtures of compounds, the preconcentration of samples, and the development of new microfluidic analytical devices.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H226,H315,H317,H319,H335

Classification des risques

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

119.3 °F - closed cup

Point d'éclair (°C)

48.5 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

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R-G Li et al.
European review for medical and pharmacological sciences, 19(12), 2213-2220 (2015-07-15)
The recent PLATINUM trial has demonstrated that the use of the new generation platinum chromium everolimus-eluting stents (PtCr-EES) yield clinical outcomes similar to those obtained by the use of cobalt chromium everolimus-eluting stents (CoCr-EES) in selected patients with 1 or
K Ishihara et al.
Journal of biomaterials applications, 13(2), 111-127 (1998-10-20)
We have synthesized phospholipid polymers containing 2-methacryloyloxyethyl phosphorylcholine (MPC) units as novel blood compatible polymers and have evaluated their interactions with blood components. It was found that in the absence of anticoagulants, blood clotting was delayed and blood cell adhesion
R Yoshida et al.
Journal of biomaterials science. Polymer edition, 3(2), 155-162 (1991-01-01)
Thermosensitive co-polymers of isopropyl acrylamide (IPAAm) with butyl methacrylate (BMA) are capable of 'on-off' regulation of drug release in response to external temperature changes due to skin formation with increasing temperature. To clarify the role of the surface-modulated skin and
Mitsuyoshi Yamane et al.
Macromolecular rapid communications, 41(18), e2000141-e2000141 (2021-01-20)
Poly(n-butyl methacrylate) (PnBMA)/reduced graphene oxide (rGO) nanocomposite films are prepared using two different routes. The first route involves preparation of PnBMA nanoparticles containing homogeneously dispersed rGO nanosheets by miniemulsion polymerization using a block copolymer of ionic liquid (IL) monomer and
K M Ahlberg et al.
International endodontic journal, 31(1), 15-21 (1998-11-21)
In this study, a methacrylate-based orthopaedic bone cement was modified for use as a root canal sealer by changing the monomer from n-butyl methacrylate to tetrahydrofurfuryl methacrylate. The sealing and bonding capabilities, solubility and handling properties of the resin were
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