Reative Monomers

Company Profile

Suzhou Senfeida Chemical Co., Ltd. was established in 2013 and is an enterprise dedicated to the production and research and development of various chemical raw materials. In order to improve production efficiency and meet customer needs, the company established a warehousing and processing plant in Changzhou, Jiangsu in 2014. Subsequently, in order to better expand the market and serve customers, the company established a contract factory in Yueyang, Hunan in 2015.In addition, in order to meet the needs of customers in different regions, the company has also established multiple contract factories in Guangdong, Shandong and other places. Through these measures, Suzhou Senfeida Chemical Co., Ltd. can better provide customers with high-quality chemical raw material products.

Why Choose Us

High quality

Our products are manufactured or executed to very high standards, using the finest materials and manufacturing processes.

Competitive Price

We offering a higher-quality product or service at an equivalent price. As a result we have a growing and loyal customer base.

Rich experience

Our company has many years of production work experience. The concept of customer-oriented and win-win cooperation makes the company more mature and stronger.

Global shipping

Our products support global shipping and the logistics system is complete, so our customers are all over the world.

After-sale service

Professional and thoughtful after -sales team, let you worry about us after -sales Intimate service, strong after -sales team support.

Advanced equipment

A machine, tool or instrument designed with advanced technology and functionality to perform highly specific tasks with greater precision, efficiency and reliability.

First 12 3 4 5 6 Last 1/6

Reative Monomers Include

What Is 2-(2-Ethoxyethoxy)Ethylacrylate

2-(2-ethoxyethoxy)ethyl acrylate is an acrylate with the chemical formula C9H16O4. It is a clear, colorless liquid with a faint odor. This compound is commonly used as a monomer in polymer synthesis, especially in the production of acrylic resins and adhesives.The acrylate group (-CH2=CHCO2-) in 2-(2-ethoxyethoxy)ethyl acrylate makes it reactive toward free radicals, enabling polymerization reactions. When polymerized, it forms polymers with acrylate functional groups that provide adhesion, hardness, and durability to the resulting material.2-(2-ethoxyethoxy)ethyl acrylate is also used as a reactive diluent in coatings, inks, and adhesive formulations. It improves the flow and rheological properties of these systems while assisting in their cross-linking and curing.

Advantages of 2-(2-Ethoxyethoxy)Ethylacrylate

Reactivity

The acrylate group (-CH2=CHCO2-) in 2-(2-ethoxyethoxy)ethyl acrylate makes it highly reactive towards free radicals, enabling polymerization reactions. This reactivity is beneficial in a variety of applications requiring polymers or cross-linked materials.

Adhesion properties

The presence of acrylate functionality in 2-(2-ethoxyethoxy)ethyl acrylate contributes to its adhesive properties. After polymerization, the resulting material has good adhesion to a variety of substrates, including metals, plastics, ceramics and wood.

Hardness and durability

Polymers formed from 2-(2-ethoxyethoxy)ethyl acrylate can exhibit desirable hardness and durability properties. This makes them suitable for applications requiring materials with mechanical strength and wear resistance.

Solubility

2-(2-ethoxyethoxy)ethyl acrylate has good solubility in a variety of organic solvents. This solubility helps it be easily incorporated into different formulations such as coatings, adhesives and resins, allowing for uniform mixing and processing.

Flexibility

Polymeric materials derived from 2-(2-ethoxyethoxy)ethyl acrylate can provide a certain degree of flexibility. This flexibility is useful for applications where elasticity and impact resistance are important, such as sealants or flexible coatings.

Cross-linking ability

The acrylate functional groups in 2-(2-ethoxyethoxy)ethyl acrylate are capable of cross-linking reactions to form a network or matrix. This cross-linking enhances the mechanical properties, durability and solvent resistance of the resulting polymer.

Types of 2-(2-Ethoxyethoxy)Ethylacrylate

Pure 2-(2-ethoxyethoxy)ethyl acrylate

This is the basic form of the compound, which contains only 2-(2-ethoxyethoxy)ethyl acrylate without any additional modifiers or functional groups. It is often used as a raw material in polymer synthesis or as a reactive diluent to adjust the viscosity and reactivity of the system.

Functionalized 2-(2-ethoxyethoxy)ethyl acrylate

This type of 2-(2-ethoxyethoxy)ethyl acrylate contains additional functional groups that can enhance its reactivity, adhesion, or other specific properties. Examples of functionalized 2-(2-ethoxyethoxy)ethyl acrylate include carboxyl-, hydroxyl-, amino-, or epoxy-functionalized versions. These modified compounds can be used in applications requiring enhanced chemical interactions or cross-linking.

Cured 2-(2-ethoxyethoxy)ethyl acrylate

After polymerization, 2-(2-ethoxyethoxy)ethyl acrylate can form a cured polymer. The cured 2-(2-ethoxyethoxy)ethyl acrylate exhibits different properties than the such as increased hardness, strength, and durability. Cured 2-(2-ethoxyethoxy)ethyl acrylate can be in the form of films, coatings, adhesives, or molded parts, depending on the application and processing method.

Copolymerized 2-(2-ethoxyethoxy)ethyl acrylate

2-(2-ethoxyethoxy)ethyl acrylate can be copolymerized with other monomers to form copolymers with desired properties. By copolymerizing with different monomers, the properties of the resulting polymer can be tailored to specific requirements, such as increased flexibility, stiffness, or adhesion.

Application of 2-(2-Ethoxyethoxy)Ethylacrylate

Polymer synthesis

2-(2-ethoxyethoxy)ethyl acrylate can be polymerized to form polymers with acrylate functionality. These polymers have excellent adhesion properties and can be used in various applications, such as coatings, adhesives, sealants, and composites.

Adhesive formulation

Due to its high reactivity and adhesion properties, 2-(2-ethoxyethoxy)ethyl acrylate is widely used in the formulation of adhesives. It can be used alone or in combination with other adhesives to bond various materials, including metals, plastics, ceramics, and woods.

Coatings and paints

2-(2-ethoxyethoxy)ethyl acrylate can be used as a reactive diluent or crosslinking agent in coatings and paints. It improves the adhesion, hardness, and durability of the coating, making it suitable for applications in automotive, industrial, and architectural coatings.

Dental materials

2-(2-ethoxyethoxy)ethyl acrylate is used in dental composites and adhesives due to its good adhesion to tooth tissue. It helps bond dental restorations and provides long-lasting adhesion.

Ink and printing

2-(2-ethoxyethoxy)ethyl acrylate can be incorporated into ink formulations to improve adhesion and printability. It is used in gravure, flexographic, and screen printing applications.

How Should 2-(2-Ethoxyethoxy)ethyl Acrylate Be Stored

2-(2-Ethoxyethoxy)ethyl acrylate should be stored in a cool, dry, and well-ventilated area, away from sources of heat, sparks, and flames. It is recommended to store it in a tightly sealed container to prevent leakage and exposure to air. The storage area should have appropriate fire protection equipment and safety measures. Additionally, it is important to follow the storage instructions provided by the manufacturer or supplier, as they may have specific recommendations based on the product's characteristics and any associated regulations or guidelines.

What Is 2-Phenoxyethyl Acrylate

2-Phenoxyethyl acrylate is an acrylate ester with the chemical formula C10H10O3. It is a colorless liquid with a faint odor. This compound is commonly used as a monomer in the synthesis of polymers, especially acrylic resins and adhesives.The acrylate group (-CH2=CHCO2-) in 2-phenoxyethyl acrylate makes it highly reactive towards free radicals, allowing it to undergo polymerization reactions. When polymerized, it forms a polymer with acrylate functionality, which can contribute to adhesion, hardness, and durability.

Advantages of 2-Phenoxyethyl Acrylate

Reactive functional group

The acrylate group (-CH2=CHCO2-) in 2-phenoxyethyl acrylate makes it highly reactive towards free radicals. This reactivity facilitates a variety of applications such as the synthesis of polymers, adhesives, and coatings. It allows cross-linking reactions to occur, resulting in the formation of a network or matrix with desired properties.

Adhesion properties

2-phenoxyethyl acrylate contributes to the adhesion properties of polymers and adhesives. When added to these materials, it can enhance bond strength between different substrates, thereby improving bonding performance. This makes it suitable for applications requiring strong adhesion, such as the automotive, construction and packaging industries.

Hardness and durability

Polymeric materials derived from 2-phenoxyethyl acrylate can exhibit desirable hardness and durability properties. This makes it useful in applications where mechanical strength and wear resistance are required of the material, such as coatings for floors, furniture or automotive parts.

Solubility

2-phenoxyethyl acrylate has good solubility in a variety of organic solvents. This solubility helps it be easily incorporated into different formulations such as coatings, adhesives and resins, allowing for uniform mixing and processing.

Flexibility

Polymeric materials derived from 2-phenoxyethyl acrylate can provide a certain degree of flexibility. This flexibility is useful for applications where elasticity and impact resistance are important, such as sealants or flexible coatings.

Types of 2-Phenoxyethyl Acrylate

Pure 2-phenoxyethyl acrylate

This is the basic form of the compound, which contains only 2-phenoxyethyl acrylate without any additional modifiers or functional groups. It is often used as a raw material in polymer synthesis or as a reactive diluent to adjust the viscosity and reactivity of the system.

Functionalized 2-phenoxyethyl acrylate

This type of 2-phenoxyethyl acrylate contains additional functional groups that can enhance its reactivity, adhesion, or other specific properties. Examples of functionalized 2-phenoxyethyl acrylate include carboxyl-, hydroxyl-, amino-, or epoxy-functionalized versions. These modified compounds can be used in applications requiring enhanced chemical interactions or cross-linking.

Cured 2-phenoxyethyl acrylate

After polymerization, 2-phenoxyethylene acrylate forms a cured polymer. Cured 2-phenoxyethyl acrylates exhibit different properties than monomers, such as increased hardness, strength, and durability. Cured 2-phenoxyethyl acrylates can be in the form of films, coatings, adhesives, or molded parts, depending on the application and processing method..

Copolymerized 2-phenoxyethyl acrylate

2-Phenoxyethyl acrylate can be copolymerized with other monomers to form copolymers with desired properties. By copolymerizing with different monomers, the properties of the resulting polymer can be tailored to specific requirements, such as increased flexibility, stiffness, or adhesion.

Application of 2-Phenoxyethyl Acrylate

Polymer synthesis: 2-Phenoxyethyl acrylate can be used as a monomer in the synthesis of polymers. When polymerized, it forms a polymer with acrylate functionality, which can contribute to adhesion, hardness, and durability. These polymers find applications in coatings, adhesives, sealants, and resins.

Adhesives and sealants: 2-Phenoxyethyl acrylate is used in the formulation of adhesives and sealants due to its reactivity towards free radicals. It can enhance the adhesion properties of these materials, making them suitable for bonding various substrates, including metals, plastics, and ceramics.

Coatings: The polymerized materials derived from 2-phenoxyethyl acrylate can be used as coatings. These coatings offer properties such as good adhesion, hardness, and chemical resistance. They can be applied to surfaces to provide protection against corrosion, abrasion, and weathering.

Ink and printing: 2-Phenoxyethyl acrylate can be incorporated into ink formulations. It can improve the adhesion of inks to substrates, enhance print quality, and increase durability. This makes it useful in printing applications, including flexographic and gravure printing.

Resin modification: 2-Phenoxyethyl acrylate can be used as a reactive diluent or modifier in resin systems. By incorporating it, the viscosity and reactivity of the resin can be adjusted, improving processing characteristics and performance.

What Is Isobornyl Acrylate

Isobornyl acrylate is a chemical compound that belongs to the class of acrylate esters. It is derived from isobornyl alcohol and acrylic acid. It is a clear liquid with a characteristic odor. Isobornyl acrylate is primarily used as a monomer in the production of various polymers and resins, particularly in the manufacturing of adhesives, coatings, and inks. It offers good adhesion, flexibility, and resistance to chemicals and weathering. Isobornyl acrylate is also used in the production of UV-curable coatings and as a reactive diluent in radiation-curable systems.

Advantages of Isobornyl Acrylate

Excellent adhesion

Isobornyl acrylate has excellent adhesive properties, making it a first choice for adhesive formulations. Materials need to withstand bending, stretching or impact without cracking or losing adhesion. It is particularly suitable for flexible packaging, automotive coatings and elastomeric materials.

Chemical resistance

Isobornyl acrylate has good resistance to a variety of chemicals, including sols, and it bonds well to a variety of substrates, including metal, plastic, glass and wood. This property ensures strong and long-lasting adhesion and is resistant to acids and alkalis. This property makes it suitable for applications where materials need to withstand corrosive chemicals, such as industrial coatings, chemical-resistant adhesives and protective coatings on metal surfaces.

Weather resistance

Isobornyl acrylate has excellent resistance to weathering, including UV radiation, moisture and temperature fluctuations. This property makes it ideal for outdoor applications such as architectural coatings, automotive finishes and protective coatings for outdoor equipment. It helps maintain appearance and performance in challenging environments.

Compatibility

Isobornyl acrylate is used as a protective coating in architectural coatings, automotive finishes and outdoor equipment. It helps maintain appearance and performance that is compatible with a variety of other monomers, polymers and additives. This compatibility enables easy formulation and blending with other materials, enabling the development of customized products with specific properties. It provides the versatility to formulate adhesives, coatings and inks to meet specific application requirements.

Low volatility

Isobornyl acrylate is less volatile, which means it evaporates slowly. This property is advantageous when the material needs to withstand bending, stretching, or impact without cracking or losing adhesion. It is particularly useful in flexible packaging applications where materials need to have longer open times, allowing for better processability and reduced waste. It is particularly useful in adhesive and coating formulations that require extended application or cure times.

Chemical resistance

During the Isob polymerization process, ac whichry islate is beneficial in providing resistance in good applications where it is critical to a variety of stabilizing chemicals, including. sol It helps prevent materials from warping, deforming or cracking, ensuring that the desired shape and size is maintained. This property is particularly important in 3D printing, casting and molding applications (venting, acids and alkalis). This property makes it suitable for applications where the material needs to withstand corrosive chemicals, for example.

Types of Isobornyl Acrylate

Isobornyl acrylate (IBOA)

This is the most common type of IBOA and is used in various applications, including adhesives, coatings, and inks. It offers excellent adhesion, flexibility, and chemical resistance.

Hydroxyethyl isobornyl acrylate (HEIBOA)

This type of IBOA contains a hydroxyethyl group, which makes it more hydrophilic than IBOA. It is used in water-based coatings and adhesives, where it offers good adhesion and water resistance.

Methoxyethyl isobornyl acrylate (MEIBOA)

This type of IBOA contains a methoxyethyl group, which makes it more hydrophobic than IBOA. It is used in solvent-based coatings and adhesives, where it offers good adhesion and solvent resistance.

Isobornyl methacrylate (IBOMA)

This is a related compound to IBOA, but it contains a methacrylate group instead of an acrylate group. It is used in various applications, including adhesives, coatings, and dental materials.

Isobornyl acrylate glycidyl ether (IBOAGE)

This type of IBOA contains a glycidyl ether group, which makes it more reactive than IBOA. It is used in UV-curable coatings and adhesives, where it offers fast curing and good adhesion.

Isobornyl acrylate urethane (IBOA-U)

This type of IBOA contains a urethane group, which makes it more flexible and durable than IBOA. It is used in various applications, including coatings, adhesives, and sealants.

Application of Isobornyl Acrylate

Polymer synthesis

Isobornyl acrylate can be used as a monomer in polymer synthesis. When polymerized, it forms polymers with acrylate functional groups that help improve adhesion, hardness, and durability. These polymers are used in coatings, adhesives, sealants and resins.

Adhesives and sealants

Due to its reactivity towards free radicals, isobornyl acrylate is used in the formulation of adhesives and sealants. It enhances the bonding properties of these materials, making them suitable for bonding to a variety of substrates, including metals, plastics and ceramics.

Paint

Polymeric materials derived from isobornyl acrylate can be used as coatings. These coatings have properties such as good adhesion, hardness and chemical resistance. They can be applied to surfaces to provide protection against corrosion, abrasion and weathering.

Ink and printing

Isobornyl acrylate can be added to ink formulations. It improves ink adhesion to the substrate, improves print quality and increases durability. This makes it very useful in printing applications, including flexographic and gravure printing.

How Should Isobornyl Acrylate Be Stored

Temperature

IBOA should be stored in a cool, dry place away from direct sunlight and heat sources. Recommended storage temperature is below 25°C (77°F). High temperatures can accelerate the polymerization process and cause product degradation.

Container

IBOA should be stored in airtight containers made of acrylate-compatible materials, such as glass or high-density polyethylene (HDPE). Make sure containers are properly labeled with product name, batch number and safety information.

Ventilation

Storage areas should be well ventilated to prevent vapor accumulation. Adequate ventilation helps maintain product quality and reduces the risk of exposure to potentially harmful fumes.

Fire Safety

IBOA is flammable and should be kept away from sources of ignition such as open flames, sparks and electrical equipment. Smoking is strictly prohibited in storage areas.

Deal with

When handling IBOA, always wear appropriate personal protective equipment (PPE), including gloves, goggles, and lab coats. Avoid direct contact with skin, eyes and clothing. In case of accidental contact, rinse the affected area with plenty of water and seek medical advice if necessary.

Compatibility

IBOA should be stored separately from incompatible materials such as oxidizers, strong acids, and alkalis. These substances can react with IBOA and cause hazardous conditions.

Our Factory

product-1-1

FAQ

Q: What is isobornyl acrylate?

A: Isobornyl acrylate, also known as 2-methyl-2-butyl acrylate, is an acrylate ester with the chemical formula C9H14O2. It is a colorless liquid with a faint odor at room temperature.

Q: What are the applications of isobornyl acrylate?

A: Isobornyl acrylate has applications in various fields, including polymer synthesis, adhesives, coatings, and inks. It can be used as a monomer to produce polymers with acrylate functionality, contributing to adhesion, hardness, and durability.

Q: What are the properties of isobornyl acrylate?

A: Isobornyl acrylate has good reactivity towards free radicals, which makes it useful in polymerization reactions. It can enhance the adhesion properties of adhesives and sealants, and provide protection and durability in coatings.

Q: How should isobornyl acrylate be stored?

A: Isobornyl acrylate should be stored in a cool, dry, and well-ventilated area, away from sources of heat, sparks, and flames. It should be kept in tightly sealed containers to prevent leakage and exposure to air.

Q: Are there any safety considerations when handling isobornyl acrylate?

A: Yes, isobornyl acrylate has certain safety considerations. It should be handled with care to avoid contact with skin and eyes. In case of contact, immediate washing with plenty of water is recommended. Proper ventilation should be ensured during handling.

Q: Can isobornyl acrylate be used in food contact applications?

A: Isobornyl acrylate is not suitable for direct food contact applications. It is used in industrial and commercial settings where it does not come into contact with food.

Q: What are the environmental impacts of isobornyl acrylate?

A: Isobornyl acrylate may have some environmental impacts. Proper disposal and handling procedures should be followed to minimize its release into the environment.

Q: Are there any regulations or restrictions on the use of isobornyl acrylate?

A: The use of isobornyl acrylate may be subject to regulations and restrictions depending on the region and application. It is important to comply with local, national, and international regulations regarding its handling, storage, and use.

Q: What is 2-(2-ethoxyethoxy)ethyl acrylate?

A: 2-(2-Ethoxyethoxy)ethyl acrylate is an acrylate ester with the chemical formula C9H16O4. It is a colorless liquid at room temperature.

Q: What are the applications of 2-(2-ethoxyethoxy)ethyl acrylate?

A: 2-(2-Ethoxyethoxy)ethyl acrylate has applications in various fields, including polymer synthesis, adhesives, coatings, and inks. It can be used as a monomer to produce polymers with acrylate functionality, contributing to adhesion, hardness, and durability.

Q: What are the properties of 2-(2-ethoxyethoxy)ethyl acrylate?

A: 2-(2-Ethoxyethoxy)ethyl acrylate has good reactivity towards free radicals, which makes it useful in polymerization reactions. It can enhance the adhesion properties of adhesives and sealants, and provide protection and durability in coatings.

Q: How should 2-(2-ethoxyethoxy)ethyl acrylate be stored?

A: 2-(2-Ethoxyethoxy)ethyl acrylate should be stored in a cool, dry, and well-ventilated area, away from sources of heat, sparks, and flames. It should be kept in tightly sealed containers to prevent leakage and exposure to air.

Q: Are there any safety considerations when handling 2-(2-ethoxyethoxy)ethyl acrylate?

A: Yes, 2-(2-ethoxyethoxy)ethyl acrylate has certain safety considerations. It should be handled with care to avoid contact with skin and eyes. In case of contact, immediate washing with plenty of water is recommended. Proper ventilation should be ensured during handling.

Q: Can 2-(2-ethoxyethoxy)ethyl acrylate be used in food contact applications?

A: 2-(2-Ethoxyethoxy)ethyl acrylate is not suitable for direct food contact applications. It is used in industrial and commercial settings where it does not come into contact with food.

Q: What are the environmental impacts of 2-(2-ethoxyethoxy)ethyl acrylate?

A: 2-(2-Ethoxyethoxy)ethyl acrylate may have some environmental impacts. Proper disposal and handling procedures should be followed to minimize its release into the environment.

Q: Are there any regulations or restrictions on the use of 2-(2-ethoxyethoxy)ethyl acrylate?

A: The use of 2-(2-ethoxyethoxy)ethyl acrylate may be subject to regulations and restrictions depending on the region and application. It is important to comply with local, national, and international regulations regarding its handling, storage, and use.

Q: What is 2-phenoxyethyl acrylate?

A: 2-Phenoxyethyl acrylate is an acrylate ester with the chemical formula C11H12O3. It is a colorless liquid at room temperature.

Q: What are the applications of 2-phenoxyethyl acrylate?

A: 2-Phenoxyethyl acrylate has applications in various fields, including polymer synthesis, adhesives, coatings, and inks. It can be used as a monomer to produce polymers with acrylate functionality, contributing to adhesion, hardness, and durability.

Q: What are the properties of 2-phenoxyethyl acrylate?

A: 2-Phenoxyethyl acrylate has good reactivity towards free radicals, which makes it useful in polymerization reactions. It can enhance the adhesion properties of adhesives and sealants, and provide protection and durability in coatings.

Q: How should 2-phenoxyethyl acrylate be stored?

A: 2-Phenoxyethyl acrylate should be stored in a cool, dry, and well-ventilated area, away from sources of heat, sparks, and flames. It should be kept in tightly sealed containers to prevent leakage and exposure to air.

As one of the leading reative monomers manufacturers and suppliers in China, we warmly welcome you to buy high-grade reative monomers made in China here from our factory. All chemicals are with high quality and low price.

Octadecyl Acrylate, Isobornyl Acrylate, CAS 32360 05 7