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Merck

235865

Butyl methacrylate

99%, contains monomethyl ether hydroquinone as inhibitor

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A propos de cet article

Formule linéaire :
CH2=C(CH3)COO(CH2)3CH3
Numéro CAS:
97-88-1
Poids moléculaire :
142.20
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24854121
EC Number:
202-615-1
Beilstein/REAXYS Number:
773960
MDL number:
MFCD00009444

Principaux documents

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Nom du produit

Butyl methacrylate, 99%, contains monomethyl ether hydroquinone as inhibitor

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

vapor density

4.91 (15 °C, vs air)

vapor pressure

2 mmHg ( 20 °C)

assay

99%

form

liquid

autoignition temp.

562 °F

contains

monomethyl ether hydroquinone as inhibitor

expl. lim.

2-8 %

refractive index

n20/D 1.423 (lit.)

bp

162-165 °C (lit.)

density

0.894 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

200

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Catégories apparentées

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.

General description

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Classe de stockage

3 - Flammable liquids

wgk

WGK 1

flash_point_f

119.3 °F - closed cup

flash_point_c

48.5 °C - closed cup

ppe

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCN6732
MKCW1148
STBL0039
MKCW4417
MKCX0115

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Consulter la Bibliothèque de documents

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
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-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 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
Ke Li et al.
Electrophoresis, 40(16-17), 2142-2148 (2019-04-30)
In this study, an in-tube solid-phase microextraction column packed with mesoporous TiO2 nanoparticles, coupled with MALDI-TOF-MS, was applied to the selective enrichment and detection of phosphopeptides in complex biological samples. The mesoporous TiO2 nanoparticles with high specific surface areas, prepared
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