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CAS:19660-16-3 | 2,3-DIBROMOPROPYL ACRYLATE

CAS:19660-16-3 | 2,3-DIBROMOPROPYL ACRYLATE

Molecular Formula:C6H8Br2O2
Molecular Weight:271.93
EINECS:243-208-9
Package:25g 100g 500g
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Made in China

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Product Introduction

Introduction of CAS:19660-16-3 | 2,3-DIBROMOPROPYL ACRYLATE

 

Molecular Structure Analysis

Molecular structure analysis of 2,3-Dibromopropyl acrylate and its polymers can be conducted using techniques like NMR and infrared spectroscopy. These techniques help in understanding the microstructure of the monomer and its polymers, providing insights into the arrangement of bromine atoms and the acrylate group within the molecule (M. Coşlkun et al., 1996).

 

Chemical Reactions and Properties

2,3-Dibromopropyl acrylate participates in various chemical reactions, especially in the formation of polymers. Its incorporation into polymers introduces bromine atoms into the polymer chains, affecting their thermal degradation behavior. The thermal degradation of such bromine-containing polymers results in the formation of monomers, HBr, CO2, and other degradation products, indicating a complex degradation mechanism that involves side chain decomposition and other reactions (N. Grassie et al., 1986).

 

Physical Properties Analysis

The physical properties of 2,3-Dibromopropyl acrylate, such as its reactivity and thermal stability, are crucial for its application in polymer synthesis. The presence of bromine significantly influences the thermal degradation and stability of the resulting polymers, with specific degradation pathways leading to various products, including brominated monomers and CO2 (N. Grassie et al., 1986).

 

Specification of CAS:19660-16-3 | 2,3-DIBROMOPROPYL ACRYLATE

 

ITEMS

SPECIFICATION

Refractive index

1.5230-1.5260

Boiling point

112/1.2mm

Density

1,77 g/cm3

Form

clear liquid

Color

Colorless to Light yellow to Light orange

 

Research Application of CAS:19660-16-3 | 2,3-DIBROMOPROPYL ACRYLATE

 

Thermal Degradation of Polymers: The thermal degradation of copolymers of methyl acrylate with 2,3-dibromopropyl acrylate is studied to understand the production of monomers and chain fragments. This research is significant in the polymer degradation field (Grassie, Diab, & Scotney, 1987).

 

Dual-Curing Acrylate Systems: 2,3-Dibromopropyl acrylate is used in dual-curing acrylate systems, which have diverse applications in shape memory polymers, optical materials, photolithography, protective coatings, and holographic materials (Konuray, Fernández‐Francos, Ramis, & Serra, 2018).

 

Copolymers for Thermal Stability and Flammability: Research on copolymers of acrylonitrile with brominated acrylates, including 2,3-dibromopropyl acrylate, shows promising thermal stability and flammability properties, making them suitable for various applications (Janović, Sarić, & Voglt, 1983).

 

Organic-Inorganic Nanocomposite Materials: The polymerization of acrylic acid in novel two-dimensional molecular spaces, such as layered aminopropylsilica, leads to the formation of organic-inorganic nanocomposite materials (Yu et al., 2007).

 

Thermoresponsive Biomaterials: The copolymerization of 2-hydroxyethyl acrylate and 2-hydroxypropyl acrylate, along with research into other acrylates, suggests potential in creating biomaterials with biocompatibility and thermoresponsive properties (Hoogenboom et al., 2009).

 

Flame-Retardant Properties in Polymers: Studies on styrene copolymers with 2,3-dibromopropyl acrylate have shown enhanced flame-retardant properties. This research is crucial for developing safer materials (Sarić, Janović, & Vogl, 1983).

 

Improvements in Flame Retardance and Mechanical Properties: Graft copolymerization of acrylic acid enhances flame retardance and mechanical properties in certain polymer blends, demonstrating the multifunctional application of acrylates (Chiang & Hu, 1996).

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