33795-49-2

Basic information

• Product Name: 11-bromoundecyl methacrylate
• Synonyms: 11-bromoundecyl methacrylate
• CAS NO: 33795-49-2
• Molecular Formula: C15H27 Br O2
• Molecular Weight: 319.28
• Mol File: 33795-49-2.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 360.3°Cat760mmHg
• Flash Point: 171.7°C
• Appearance: /
• Density: 1.109g/cm³
• Vapor Pressure: 2.25E-05mmHg at 25°C
• Refractive Index: 1.472
• CAS DataBase Reference: 11-bromoundecyl methacrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 11-bromoundecyl methacrylate(33795-49-2)
• EPA Substance Registry System: 11-bromoundecyl methacrylate(33795-49-2)

Safety Data

• Hazardous Substances Data: 33795-49-2(Hazardous Substances Data)

Usage

General Description

11-bromoundecyl methacrylate is a chemical compound with the molecular formula C15H27BrO2. It is a methacrylate monomer that is commonly used in the production of polymers and copolymers for various industrial applications. 11-bromoundecyl methacrylate is a highly reactive and versatile monomer that can undergo free radical polymerization to form polymers with desirable properties such as flexibility, chemical resistance, and adhesion. It is often used in the production of adhesives, coatings, and functional materials. Additionally, the bromine group in its structure allows for further chemical modifications and functionalization, making it a valuable building block in the synthesis of advanced materials.

InChI:InChI=1/C15H27BrO2/c1-14(2)15(17)18-13-11-9-7-5-3-4-6-8-10-12-16/h1,3-13H2,2H3

Upstream product

• 1611-56-9 1-Bromo-11-hydroxyundecane 
• 80-62-6 methacrylic acid methyl ester 
• 2834-05-1 11-bromoundecanoic acid 
• 1122-58-3 dmap 
• 546-68-9 titanium(IV) isopropylate 
• 4245-37-8 vinyl methacrylate 
• 920-46-7 Methacryloyl chloride 

Relevant articles and documents

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A highly efficient preparation of methacrylate esters using novel solid phase titanium-based transesterification catalysts

Highly active transesterification catalysts for the synthesis of sensitive methacrylate monomers can be conveniently prepared by reacting chlorotriisopropoxy titanium with cross-linked polystyrene beads functionalised with acetyl acetone or polyethylene glycol ligands.

Polymerization of wormlike micelles induced by hydrotropic salt

Addition of the hydrotropic salt sodium tosylate (TSNa) to solutions of a polymerizable cationic surfactant, methacryloyloxyundecyltrimethylammonium bromide (MUTB), leads to a transition from spherical to wormlike micelles about 40 nm in length. The wormlike micelles were successfully polymerized to yield stable, single-phase solutions of polymerized micelles. The polymerized wormlike micelles were several hundred nanometers long, although their cross-sectional radius remained unchanged (～2 nm). The spherical to wormlike micelle transition, and the wormlike micelles polymerized at different molar ratios of TSNa to MUTB, were characterized using quasi-elastic and static light scattering, small-angle neutron scattering, NMR, and cryogenic transmission electron microscopy.

POLYMERIZABLE COMPOUNDS WITH ONE OR MORE SURFACTANT-LIKE PROPERTIES

Some embodiments of the present disclosure relate to polymerizable compounds that comprise biocidal activity and/or the potential for increased biocidal activity and that comprise at least one hydrophobic portion and at least one hydrophilic portion. Together the hydrophobic portion and the hydrophilic portion of the compounds may provide the polymerizable compounds with one or more surfactant-like properties. The polymerizable compounds can be incorporated into polymer coating formulations. The polymer coating formulations can be used to coat one or more surfaces of a substrate. The coating formulation can provide biocidal activity and/or the potential for increased biocidal activity to the coated substrate-surface.