9003-63-8

Basic information

• Product Name: POLY(N-BUTYL METHACRYLATE)
• Synonyms: 2-Propenoicacid,2-methyl-,butylester,homopolymer;Butyl2-methyl-2-propenoate,homopolymer;butyl2-methyl-2-propenoatehomopolymer;Butylmethacrylatehomopolymer;methacrylicacid,butylester,polymers;Methacrylicacid,butylesterhomopolymer;N-BUTYL METHACRYLATE (POLYMER);N-BUTYL METHACRYLATE RESIN
• CAS NO: 9003-63-8
• Molecular Formula: (C10H20O2)n
• Molecular Weight: 142.2
• EINECS: 202-615-1
• Product Categories: Hydrophobic Polymers;Methacrylate PolymersSelf Assembly&Contact Printing;PMMA-Based Resins;Stamps for Nanoprint Lithography&Microcontact Printing;Poly(butyl methacrylate);Alphabetic;Organic Soluble Polymers;P;POLB - POLYPolymer Standards;Polymers;Acrylics;Methacrylate Polymers;Microcontact Printing;PMMA-Based Resins;Stamps for Nanoprint Lithography &Contact Printing;Hydrophobic Polymers;Materials Science;Micro/NanoElectronics;Polymer Science;Self Assembly &
• Mol File: 9003-63-8.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 160°Cat760mmHg
• Flash Point: 50.6°C
• Appearance: /powder
• Density: 1.07 g/mL at 25 °C(lit.)
• Vapor Pressure: 2.44mmHg at 25°C
• Refractive Index: n20/D 1.483
• CAS DataBase Reference: POLY(N-BUTYL METHACRYLATE)(CAS DataBase Reference)
• NIST Chemistry Reference: POLY(N-BUTYL METHACRYLATE)(9003-63-8)
• EPA Substance Registry System: POLY(N-BUTYL METHACRYLATE)(9003-63-8)

Safety Data

• Hazard Codes: Xi
• Statements: 10-36/37/38-43
• Safety Statements: 24/25
• WGK Germany: 1
• RTECS: UD3399000
• Hazardous Substances Data: 9003-63-8(Hazardous Substances Data)

Usage

Description

Poly(N-butyl methacrylate), also known as PBMA, is a type of polymer that is formed from the polymerization of N-butyl methacrylate monomers. It is a transparent, amorphous polymer with excellent optical properties, making it suitable for various applications in different industries.

Uses

Used in Optical Applications:
PBMA is used as a polymer matrix for embedding photoluminescent materials, such as EuTFC, in polymer films. This allows for the study of photoluminescence properties, which can be useful in various optical applications, including sensors, displays, and lighting.
Used in Research and Development:
PBMA is used as a substrate for studying the properties and behavior of various materials, such as photoluminescent materials, when embedded in a polymer matrix. This can help researchers understand the interactions between the embedded materials and the polymer, as well as optimize the performance of the resulting composite materials.
Used in Coatings and Adhesives:
Due to its excellent optical properties and flexibility, PBMA can be used as a component in coatings and adhesives for various applications, such as automotive, architectural, and electronic industries. It can provide improved adhesion, durability, and optical clarity to the final product.
Used in Biomedical Applications:
PBMA's biocompatibility and optical properties make it a potential candidate for use in biomedical applications, such as drug delivery systems, tissue engineering, and medical imaging. It can be used to encapsulate drugs or other bioactive agents, providing controlled release and improved therapeutic outcomes.

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

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Relevant articles and documents

An efficient, practical and cost-effective polymer-supported catalyst for the transesterification of methyl methacrylate by 1-butanol

A straightforward and cost-effective synthesis of a polymer-supported titanium alkoxide catalyst is reported. The described synthesis involves cheap, readily available and relatively non toxic chemicals, solvents and workup procedures. Efficiency and stability of the catalyst were tested in a laboratory-scale continuous flow reactor under equilibrium conditions over a month period. The average daily titanium leaching was estimated to less than 1% of the total amount of titanium engaged. To our knowledge, this result is the best obtained, to date, concerning the use of heterogeneous titanate for the catalysis of transesterification reactions.

Silica-Supported MnII Sites as Efficient Catalysts for Carbonyl Hydroboration, Hydrosilylation, and Transesterification

Manganese, the third most abundant transition-metal element after iron and titanium, has recently been demonstrated to be an effective homogeneous catalyst in numerous reactions. Herein, the preparation of silica-supported MnII sites is reported using Surface Organometallic Chemistry (SOMC), combined with tailored thermolytic molecular precursors approach based on Mn2[OSi(OtBu)3]4 and Mn{N(SiMe3)2}2?THF. These supported MnII sites, free of organic ligands, efficiently catalyze numerous reactions: hydroboration and hydrosilylation of ketones and aldehydes as well as the transesterification of industrially relevant substrates.

METHOD FOR THE PRODUCTION PROCESS OF BUTYL METHACRYLATE

The present invention relates to a preparation method of butyl methacrylate, which comprises the steps of: a) preparing butyl methacrylate through ester exchange reaction of n-butanol and methyl methacrylate in the presence of titanium tetrabutoxide catalyst; and b) removing the catalyst by adding glycerol to butyl methacrylate after the ester exchange reaction. The preparation method of butyl methacrylate in the present invention improves removal rate of residual solvents remaining after recovering the products after the ester exchange reaction, and has the catalyst removal process at low costs.COPYRIGHT KIPO 2016