99% White Powder Dicyclopentanyl methacrylate CAS NO (34759-34-7) At Cheap Price

1. Chemical Structure and Identity:

Dicyclopentanyl methacrylate, with the chemical formula C14H20O2, is an organic compound belonging to the class of methacrylate esters. It is characterized by the presence of a methacrylate functional group (-C=C-COOCH3) attached to a cyclopentyl group.

2. Synthesis and Production:

Dicyclopentanyl methacrylate can be synthesized through the esterification reaction between methacrylic acid and cyclopentanol, followed by purification steps to isolate the desired product. Alternatively, it can be prepared by reacting methacryloyl chloride with cyclopentanol in the presence of a base.

3. Physical Properties:

• Appearance: Dicyclopentanyl methacrylate is commonly found as a clear, colorless liquid.
• Boiling Point: It has a boiling point typically between 180°C to 185°C.
• Solubility: It is soluble in common organic solvents such as ethanol, methanol, acetone, and dichloromethane.

4. Applications and Uses:

Dicyclopentanyl methacrylate finds application in various fields, including polymer chemistry, coatings, adhesives, and biomedical research. Some of its uses include:

• Copolymerization: It serves as a monomer in copolymerization reactions with other methacrylate monomers to produce polymers with desired properties, such as flexibility, toughness, and chemical resistance.
• Coatings and Adhesives: Dicyclopentanyl methacrylate is utilized in the formulation of coatings, adhesives, and sealants for applications requiring enhanced adhesion, flexibility, and durability.
• Biomedical Research: It is used as a functional monomer in the synthesis of hydrogels and biomaterials for drug delivery, tissue engineering, and biomedical diagnostics applications due to its biocompatibility and versatility.

5. Polymerization Mechanism:

Dicyclopentanyl methacrylate undergoes radical polymerization reactions, where initiator molecules initiate the formation of polymer chains by reacting with the double bond (-C=C-) present in the methacrylate functional group. This results in the formation of polymers with pendant cyclopentyl groups, which impart specific properties to the polymer.

6. Safety and Handling:

While specific safety data may vary, dicyclopentanyl methacrylate should be handled with care due to its potential irritant and sensitizing properties. It is recommended to use appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Additionally, proper ventilation should be ensured to minimize exposure to airborne vapors.

7. Environmental Impact:

The environmental impact of dicyclopentanyl methacrylate may depend on factors such as its use, disposal, and potential for release into the environment. As with any chemical compound, it is important to handle and dispose of dicyclopentanyl methacrylate in accordance with relevant regulations to minimize adverse effects on the environment.

8. Regulatory Considerations:

Dicyclopentanyl methacrylate may be subject to regulations and guidelines governing its production, handling, transportation, and use, particularly in biomedical research and industrial applications. Compliance with these regulations is essential to ensure safety, environmental protection, and regulatory compliance.

In summary, dicyclopentanyl methacrylate is an organic compound with diverse applications in polymer chemistry, coatings, adhesives, and biomedical research. Its synthesis, physical properties, uses, polymerization mechanism, safety considerations, environmental impact, and regulatory aspects are important factors to consider in its production, handling, and utilization.