Skip to Content
Merck
CN

235865

Butyl methacrylate

99%, contains monomethyl ether hydroquinone as inhibitor

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
CH2=C(CH3)COO(CH2)3CH3
CAS Number:
Molecular Weight:
142.20
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-615-1
Beilstein/REAXYS Number:
773960
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


vapor density

4.91 (15 °C, vs air)

Quality Level

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

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

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.


Still not finding the right product?

Explore all of our products under Butyl methacrylate


pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

Regulatory Information

危险化学品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library


Articles

组织工程已成为治疗受损或患病的器官和组织(例如血管和尿囊)的关键治疗工具。

Tissue engineering has become a key therapeutic tool in the treatment of damaged or diseased organs and tissues, such as blood vessels and urinary bladders.


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
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



Global Trade Item Number

SKUGTIN
235865-100ML04061837399510
235865-18L04061837399527
235865-1L04061838785282