Butyl methacrylate (BMA) - ≥99%, Containing MEHQ stabilizer , CAS No.97-88-1

CAS: 97-88-1 Cat. No.: B110902 Formula: C₈H₁₄O₂ Molecular Weight: 142.2 Beilstein Registry Number: 773960 EC Number: 202-615-1

GRADE & PURITY ≥99%, Containing MEHQ stabilizer

Synonyms

N-Butyl methacrylate | Methacrylic Acid Butyl Ester | Butylmethacrylate | butyl 2-methylprop-2-enoate

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Overview

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.

Specifications

Synonyms

N-Butyl methacrylate | Methacrylic Acid Butyl Ester | Butylmethacrylate | butyl 2-methylprop-2-enoate

Specifications & Purity

≥99%, Containing MEHQ stabilizer

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥99%

Names and Identifiers

Pubchem Sid

508814850

Canonical Smiles

CCCCOC(=O)C(=C)C

IUPAC Name

butyl 2-methylprop-2-enoate

InChIKey

SOGAXMICEFXMKE-UHFFFAOYSA-N

INCHI

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

Isomeric SMILES

CCCCOC(=O)C(=C)C

WGK Germany

1

RTECS

OZ3675000

UN Number

2227

Packing Group

III

Molecular Weight

142.2

Beilstein

773960

Reaxy-Rn

773960

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773960&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid esters
          • Level6 Alpha,beta-unsaturated carboxylic esters
            • Level7 Enoate esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters
• Direct Parent: Enoate esters
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Miscible with ethyl ether and ethanol. Immiscible with water.
• Refractive Index: 1.4229
• Flash Point(°F): 129.2 °F
• Flash Point(°C): 41℃
• Boil Point(°C): 160-163°C
• Melt Point(°C): -75°C
• Molecular Weight: 142.200 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 142.099 Da
• Monoisotopic Mass: 142.099 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 127.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1