24910-84-7

Basic information

• Product Name: 2,3-dichloropropyl acrylate
• Synonyms: 2,3-dichloropropyl acrylate;Acrylic acid 2,3-dichloropropyl ester;2-Propenoic acid, 2,3-dichloropropyl ester;Einecs 246-527-1
• CAS NO: 24910-84-7
• Molecular Formula: C₆H₈Cl₂O₂
• Molecular Weight: 183.03252
• EINECS: 246-527-1
• Mol File: 24910-84-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 247.1°C at 760 mmHg
• Flash Point: 106.1°C
• Appearance: /
• Density: 1.225g/cm³
• Vapor Pressure: 0.0262mmHg at 25°C
• Refractive Index: 1.461
• CAS DataBase Reference: 2,3-dichloropropyl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dichloropropyl acrylate(24910-84-7)
• EPA Substance Registry System: 2,3-dichloropropyl acrylate(24910-84-7)

Safety Data

• Hazardous Substances Data: 24910-84-7(Hazardous Substances Data)

Usage

General Description

2,3-dichloropropyl acrylate is a chemical compound with the molecular formula C6H8Cl2O2. It is a clear, colorless liquid that is commonly used in the production of adhesives, coatings, and resins. 2,3-dichloropropyl acrylate is known for its ability to undergo polymerization, which makes it useful in the creation of various polymers that have applications in a wide range of industries. However, 2,3-dichloropropyl acrylate is also classified as a hazardous substance, as it can cause skin and eye irritation, and can be harmful if inhaled or ingested. Therefore, proper precautions and handling procedures are necessary when working with this chemical.

InChI:InChI=1/C6H8Cl2O2/c1-2-6(9)10-4-5(8)3-7/h2,5H,1,3-4H2

Upstream product

• 616-23-9 2,3-Dichloro-1-propanol 
• 140-88-5 ethyl acrylate 
• 7208-96-0 2-chloro-1-(chloromethyl)ethyl dodecanoate 

Downstream Products

• 616-23-9 2,3-Dichloro-1-propanol 

Relevant articles and documents

Biocatalytic preparation of dichloropropyl acrylates. Application to the synthesis of poly(dichloropropyl acrylates)

The synthesis of dichloropropyl acrylates from dichloropropyl dodecanoates through a transesterification process using diverse commercial lipases and whole cells (fungal resting cells) is presented. The synthesis was carried out in a solvent-free media using a conventional batch system and a packed bed reactor (PBR). The effect of water activity on the process depended on the lipase used. The commercial enzyme CALB (Candida antarctica lipase B immobilized onto a macroporous acrylic resin) showed the best performance as a biocatalyst, achieving a yield of 50% and productivity of 7.2 μmol min-1 g -1 in the batch reactor and 33% and 35.8 μmol min-1 g-1 in the PBR. Finally, polymeric material was prepared by suspension polymerization of the dichloropropyl acrylates synthesized using PBR. Particles with diameters between 170 and 380 μm were obtained with a yield of 85% after 18 h reaction. AbbreviationsPBRpacked bed reactorCALBCandida antarctica lipase B immobilized onto a macroporous acrylic resin.