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2,2,3,3-tetrafluoropropyl Methacrylate


Properties
Product Name 2,2,3,3-Tetrafluoropropyl methacrylate
Cas Number 45115-41-3
Formula C7H8F4O2
Molar Mass 200.13
Boiling Point 95-98°C
Density 1.286 g/cm³
Refractive Index 1.37
Flash Point 107°F
Appearance Clear liquid
Odor Characteristic
Viscosity 2-3 cP
Solubility Insoluble in water
Stability Stable under recommended conditions
Storage Temperature Keep container tightly closed in a dry and well-ventilated place.
Hazard Statements Use personal protective equipment as required; Avoid contact with skin and eyes.
FAQ

What are the main applications of 2,2,3,3-tetrafluoropropyl methacrylate?

2,2,3,3 - tetrafluoropropyl methacrylate is a fluorinated monomer with several important applications.The 2,2,3,3-tetrafluoropropylmethacrylate monomer has several important applications.
One of the main applications is in the coatings industry.Coatings is one of the most common applications. Fluorinated coatings offer unique properties such as excellent chemical resistance, weather resistance, and low surface energy.Fluorinated paints have unique properties, such as chemical resistance, weather resistance and low surface energy. Coatings formulated with 2,2,3,3 - tetrafluoropropyl methacrylate can be used on a variety of substrates, including metals, plastics, and glass.Coatings formulated using 2,2,3,3-tetrafluoropropylmethacrylate are suitable for a wide range of substrates including metals and plastics. For example, in the automotive industry, these coatings can be applied to car bodies to protect against corrosion, scratches, and environmental factors like UV radiation and acid rain.In the automotive industry, for example, these coatings are applied to car body panels to protect them from corrosion, scratches and environmental factors such as UV radiation and acid rainfall. The low surface energy of the fluorinated coatings also makes them dirt - and water - repellent, keeping the vehicle's surface clean for longer periods.The fluorinated coatings have a low surface energy, which makes them dirt- and water-repellent. This helps to keep the vehicle's surface cleaner for longer.

In the field of adhesives, this monomer can enhance the performance of adhesive formulations.This monomer can improve the performance of adhesive formulations. It can improve the adhesion to a wide range of materials while also providing chemical and heat resistance.It can enhance adhesion with a variety of materials, while also providing chemical resistance and heat resistance. In electronics manufacturing, adhesives with 2,2,3,3 - tetrafluoropropyl methacrylate can be used to bond components.In electronics manufacturing adhesives containing 2,2,3,3-tetrafluoropropylmethacrylate are used to bond components. They can withstand the harsh conditions inside electronic devices, such as temperature variations during operation, and maintain a strong bond over time.They can withstand harsh conditions in electronic devices, including temperature fluctuations during operation, and still maintain a strong adhesive over time.

Another application area is in the production of polymers for optical devices.Polymers for optical devices is another application area. Polymers containing 2,2,3,3 - tetrafluoropropyl methacrylate can have good optical transparency, low refractive index, and excellent thermal stability.Polymers containing 2,2,3,3-tetrafluoropropylmethacrylate have excellent thermal stability, a low refractive indices, and good optical transparency. These properties make them suitable for use in optical fibers, lenses, and waveguides.These properties make these polymers suitable for use in optical fibres, lenses, or waveguides. For instance, in optical fibers, the fluorinated polymer can help reduce signal loss and improve the overall performance of the communication system.In optical fibers, for example, the fluorinated material can reduce signal loss, and improve the performance of the communication system.

It is also used in the synthesis of specialty polymers for biomedical applications.It is also used to synthesize specialty polymers for biomedical purposes. The chemical resistance and biocompatibility of polymers derived from this monomer make them potentially useful for medical devices.Polymers derived from monomer are biocompatible and chemically resistant, making them useful for medical devices. They can be used to coat implants to prevent the adhesion of bacteria and reduce the risk of infections.They can be used as a coating on implants to reduce the risk of infection and prevent bacteria adhesion. Additionally, these polymers may be used in drug delivery systems, where their unique properties can help control the release of drugs over time.These polymers can also be used to control the release of drugs in drug delivery systems.

Overall, 2,2,3,3 - tetrafluoropropyl methacrylate plays a significant role in various industries, enabling the development of high - performance materials with enhanced properties.Overall, 2,2,3,3-tetrafluoropropylmethacrylate is a key component in the development of high-performance materials with enhanced properties.

What are the physical and chemical properties of 2,2,3,3-tetrafluoropropyl methacrylate?

2,2,3,3 - tetrafluoropropyl methacrylate is an important fluorinated monomer with distinct physical and chemical properties.The 2,2,3,3-tetrafluoropropylmethacrylate is a fluorinated monomer that has distinct physical and chemical characteristics.
Physical properties:Physical Properties
1. Appearance: It is typically a colorless to light - yellow liquid under normal conditions.Appearance: Under normal conditions, it is a colorless or light-yellow liquid. This clear - liquid state makes it easy to handle and mix with other substances in various applications, such as in the formulation of coatings or polymers.This clear liquid state makes it easier to handle and mix in different applications, like the formulation of polymers or coatings.
2. Boiling point: Its boiling point is influenced by the fluorine - containing groups.Boiling point - Its boiling point can be affected by the presence of fluorine groups. Fluorine atoms increase the intermolecular forces due to their high electronegativity.Fluorine atoms are known for their high electronegativity, which increases the intermolecular force. Generally, it has a boiling point that allows it to be processed within a certain temperature range suitable for industrial operations.It has a boiling temperature that allows it be processed within a range of temperatures suitable for industrial applications. For example, it may boil at a temperature that enables it to be vaporized and condensed in distillation processes for purification.It may boil at a certain temperature, allowing it to be vaporized in distillation processes and then condensed.
3. Density: The density of 2,2,3,3 - tetrafluoropropyl methacrylate is relatively higher than that of many non - fluorinated analogs.Density: The 2,2,3,3-tetrafluoropropylmethacrylate density is higher than many of its non-fluorinated analogues. The presence of fluorine atoms, which are heavier than hydrogen atoms, contributes to this increase in density.This increase in density is due to the presence of heavier fluorine atoms than hydrogen atoms. This property can be significant in applications where the mass - volume relationship is crucial, like in the preparation of formulations with specific weight - volume ratios.This property is important in applications where the mass-volume relationship is critical, such as in the preparation formulas with specific weight-volume ratios.
4. Viscosity: It usually has a relatively low viscosity.It has a low viscosity. This low viscosity allows for good flowability, which is beneficial when it is used as a monomer in polymerization reactions.This low viscosity makes it easy to flow, which is useful when used as a polymerization monomer. It can easily spread and penetrate into substrates, facilitating the formation of uniform coatings or polymers.It can easily spread out and penetrate substrates, facilitating uniform coatings or polymers.

Chemical properties:Chemical properties
1. Polymerizability: As a methacrylate monomer, 2,2,3,3 - tetrafluoropropyl methacrylate has a reactive double bond.Polymerizability - As a monomer of 2,2,3,3-tetrafluoropropylmethacrylate, it has a reactive double link. This double bond can participate in polymerization reactions, such as free - radical polymerization.This double bond is capable of participating in polymerization reactions such as free radical polymerization. When initiated, it can form polymers or copolymers.It can be initiated to form polymers or copolymers. For instance, it can be copolymerized with other methacrylate monomers to introduce fluorine - containing segments into the polymer chain, thereby imparting unique properties like water and oil repellency to the resulting copolymer.It can be copolymerized to introduce fluorine-containing segments into the polymer chains, giving the resulting copolymer unique properties such as water and oil repellency.
2. Chemical stability: The fluorine - carbon bonds in 2,2,3,3 - tetrafluoropropyl methacrylate are very strong.Chemical stability: The bonds between fluorine and carbon in 2,2,3,3- tetrafluoropropylmethacrylate are very stable. This gives the compound good chemical stability.This gives the compound a good chemical stability. It is resistant to many common chemicals, including acids, bases, and oxidizing agents to a certain extent.It is resistant to a number of common chemicals including acids, bases and oxidizing agents. This property makes it suitable for use in environments where chemical resistance is required, such as in coatings for chemical storage tanks or in industrial applications exposed to harsh chemical conditions.This property makes it ideal for environments that require chemical resistance, such as coatings for chemical storage tank or industrial applications exposed harsh chemical conditions.
3. Surface - active properties: The fluorine - containing groups in the molecule confer surface - active properties.Surface-active properties: The fluorine-containing groups in the molecules confer surface-active properties. It has a tendency to migrate to the surface of polymers or coatings during the formation process.During the formation process, it has a tendency for the fluorine to migrate to surfaces of polymers or coatings. This results in materials with low surface energy, which can lead to improved wetting, anti - adhesion, and self - cleaning properties.This can result in materials that have low surface energy. This can lead to better wetting, anti-adhesion, and self-cleaning properties. For example, coatings made from polymers containing 2,2,3,3 - tetrafluoropropyl methacrylate may prevent dirt and water from adhering easily.For example, coatings containing 2,2,3,3-tetrafluoropropylmethacrylate can prevent dirt and moisture from adhering.

How is 2,2,3,3-tetrafluoropropyl methacrylate synthesized?

The synthesis of 2,2,3,3 - tetrafluoropropyl methacrylate can be achieved through the following general approach.The following general approach can be used to synthesize 2,2,3,3-tetrafluoropropylmethacrylate.
Starting Materials Preparation
Typically, 2,2,3,3 - tetrafluoropropanol is one of the key starting materials.2,2,3,3-tetrafluoropropanol, is usually one of the main starting materials. This alcohol can be obtained through various fluorination reactions.This alcohol can be produced by various fluorination processes. For example, it may be synthesized from appropriate halogen - containing propanol precursors via fluorination using fluorinating agents such as hydrogen fluoride in the presence of catalysts.It can be made from halogen-containing propanols by fluorination, using fluorinating substances such as hydrogen fluoride and catalysts.

Esterification Reaction
The main step in the synthesis of 2,2,3,3 - tetrafluoropropyl methacrylate is the esterification reaction between 2,2,3,3 - tetrafluoropropanol and methacrylic acid.The esterification between 2,2,3,3-tetrafluoropropanol, and methacrylic acids is the main step in the synthesizing of 2,2,3,3-tetrafluoropropylmethacrylate. This reaction is usually catalyzed.This reaction is normally catalyzed. A common catalyst for this type of esterification is a strong acid, such as sulfuric acid or p - toluenesulfonic acid.This type of esterification can be catalyzed by a strong acid such as sulfuric or p-toluenesulfonic acids.

In a typical procedure, 2,2,3,3 - tetrafluoropropanol and methacrylic acid are mixed in an appropriate molar ratio, often with a slight excess of one of the reactants to drive the reaction forward according to Le Chatelier's principle.In a typical procedure 2,2,3,3-tetrafluoropropanol, and methacrylic are mixed in a molar proportion, sometimes with a slight overabundance of one of them to drive the reaction along according to Le Chatelier’s principle. The catalyst is added in a small amount, usually a few mole percent relative to the reactants.The catalyst is usually added in small amounts, usually a few mol% relative to the reactants.

The reaction mixture is then heated to an appropriate temperature, usually in the range of 80 - 120 degC, under reflux conditions.Under reflux conditions, the reaction mixture is heated to a temperature that is suitable, usually between 80 and 120 degC. A reflux condenser is used to prevent the loss of volatile components.To prevent volatile components from being lost, a reflux condenser can be used. As the reaction proceeds, water is produced as a by - product.Water is produced by the reaction. To shift the equilibrium towards the formation of the ester, water can be removed from the reaction system.Water can be removed from the system to shift the equilibrium in favor of the ester. This can be achieved by using azeotropic distillation with an appropriate solvent, such as toluene or benzene, which forms an azeotrope with water and can be distilled out of the reaction mixture.This can be achieved using azeotropic distillation with a suitable solvent, such a toluene.

Purification
After the reaction is complete, as determined by techniques such as gas chromatography or nuclear magnetic resonance spectroscopy, the reaction mixture needs to be purified.Purification is required after the reaction has been completed, as determined using techniques such as nuclear magnetic resonance spectroscopy or gas chromatography. First, the catalyst is neutralized, for example, by adding a base such as sodium carbonate or sodium hydroxide solution.The catalyst is neutralized first, for instance, by adding a base, such as sodium hydroxide or sodium carbonate solution. This will form a salt that can be separated from the organic layer.This will produce a salt which can be separated from organic layer.
The organic layer containing the 2,2,3,3 - tetrafluoropropyl methacrylate is then washed several times with water to remove any remaining salts and unreacted polar components.The organic layer containing 2,2,3,3-tetrafluoropropylmethacrylate must be washed with water several times to remove any salts or unreacted polar component. Finally, the product can be further purified by distillation under reduced pressure to obtain pure 2,2,3,3 - tetrafluoropropyl methacrylate.The product can then be further purified using reduced pressure distillation to obtain pure 2,2,3,3-tetrafluoropropylmethacrylate. This distillation step helps to separate the product from any remaining unreacted starting materials and high - boiling impurities.This step helps separate the product from unreacted starting materials, high-boiling impurities and any remaining unreacted starter materials.

What are the safety precautions when handling 2,2,3,3-tetrafluoropropyl methacrylate?

2,2,3,3 - tetrafluoropropyl methacrylate is a chemical compound that requires certain safety precautions during handling.Tetrafluoropropyl Methacrylate, also known as 2,2,3,3, is a chemical that requires special precautions when handling.
First, in terms of personal protective equipment.Personal protective equipment is the first thing to consider. Wear appropriate chemical - resistant gloves.Wear gloves that are resistant to chemicals. Nitrile or neoprene gloves are often good choices as they can resist the potential chemical contact from this substance.These gloves can resist chemical contact. This helps prevent skin absorption, which could lead to various health issues such as skin irritation or more serious systemic effects.This prevents skin absorption that could lead to skin irritation and other serious systemic effects. Additionally, wear safety goggles or a face shield.Wear safety goggles, or a face shield. This protects the eyes from any splashes that might occur during handling.This will protect your eyes from any splashes you may encounter during handling. If the chemical gets into the eyes, it can cause severe irritation, damage to the cornea, and potential vision impairment.If the chemical gets in the eyes, it may cause severe irritation, corneal damage, and even vision impairment.

Ventilation is crucial.Ventilation is essential. Ensure that the area where the 2,2,3,3 - tetrafluoropropyl methacrylate is being handled has adequate ventilation.Make sure that the area in which the 2,2,3,3-tetrafluoropropylmethacrylate is handled has adequate ventilation. This can be achieved through natural ventilation if possible, but in most industrial or laboratory settings, mechanical ventilation systems like exhaust hoods are necessary.If possible, this can be achieved by using natural ventilation, but in industrial or laboratory settings mechanical ventilation systems such as exhaust hoods may be necessary. Good ventilation helps to prevent the build - up of vapors.A good ventilation system can prevent the accumulation of vapors. Inhalation of the vapors can irritate the respiratory tract, causing coughing, shortness of breath, and may even lead to more serious lung problems over time.Inhaling the vapors may cause irritation to the respiratory tract. This can lead to coughing and shortness of breathe, or even more serious lung conditions over time.

When storing this compound, keep it in a cool, dry place away from sources of ignition.Store this compound in a dry, cool place, away from ignition sources. It is flammable, so any potential heat sources, open flames, or electrical sparks should be avoided.It is flammable so avoid any heat sources, open fires or electrical sparks. Store it in a container that is tightly sealed to prevent leakage and evaporation.Store it in a tightly sealed container to prevent leaking and evaporation. Label the storage container clearly with the name of the chemical, its concentration, and any relevant hazard warnings.Label the container with the name of chemical, its concentration and any relevant warnings. This ensures that anyone who comes across the container is aware of the potential dangers.This will ensure that anyone who comes into contact with the container is aware of any potential dangers.

During handling operations, avoid creating aerosols or dusts.Avoid creating aerosols and dusts during handling operations. When transferring the chemical from one container to another, do it carefully to prevent splashing.Transferring the chemical from one container into another should be done carefully to avoid splashing. If a spill occurs, immediately take appropriate measures.Take immediate action if a spill happens. First, evacuate the area if the spill is large enough to pose a significant vapor or inhalation risk.If the spill is large and poses a significant inhalation or vapor risk, you should evacuate the area. Then, use absorbent materials like sand or vermiculite to contain the spill.Use absorbent materials such as sand or Vermiculite to contain spills. Do not use water to clean up the spill unless it is specifically recommended for this chemical, as water may not be effective and could potentially spread the chemical.Water may not be an effective way to clean up a spill, and it could spread the chemical. After cleaning up the spill, dispose of the contaminated absorbent materials properly according to local regulations.After cleaning the spill, dispose the contaminated absorbent material according to local regulations.

Finally, be aware of the potential reactivity of 2,2,3,3 - tetrafluoropropyl methacrylate.Be aware of the potential for reactivity when using 2,2,3,3- tetrafluoropropylmethacrylate. It may react with certain substances, so keep it away from strong oxidizing agents, acids, and bases.Keep it away from strong acids, bases, and oxidizing agents. Understanding its chemical reactivity helps prevent unexpected and potentially dangerous chemical reactions.Understanding its chemical reactivity can help prevent unexpected and potentially hazardous chemical reactions.

What are the storage requirements for 2,2,3,3-tetrafluoropropyl methacrylate?

2,2,3,3 - tetrafluoropropyl methacrylate is a chemical compound that has specific storage requirements to ensure its stability, safety, and integrity.Tetrafluoropropyl Methacrylate, also known as 2,2,3,3, is a chemical compound with specific storage requirements. These are designed to ensure stability, safety and integrity.
Firstly, storage should be in a cool and well - ventilated area.First, the storage area should be cool and well-ventilated. High temperatures can accelerate chemical reactions, such as polymerization.High temperatures can speed up chemical reactions such as polymerization. If the compound is exposed to heat for an extended period, it may start to polymerize spontaneously, which can change its chemical properties and render it unusable for its intended applications.If the compound is exposed for a long time to heat, it can start to polymerize, which can change chemical properties, making it unusable. A temperature range of around 2 - 8 degC is often ideal for storage, similar to the conditions in a common refrigerator used for chemical storage.The ideal temperature range for storage is usually between 2 and 8 degC, which is similar to the conditions found in a refrigerator that's used for chemical storage.

Secondly, it must be stored away from sources of ignition.Second, it should be stored away from ignition sources. 2,2,3,3 - tetrafluoropropyl methacrylate is likely to be flammable.It is likely that 2,2,3,3-tetrafluoropropylmethacrylate will be flammable. This means that any open flames, sparks from electrical equipment, or other potential ignition sources in the storage area can pose a significant fire hazard.This means that open flames, sparks generated by electrical equipment, and other ignition sources within the storage area could pose a serious fire risk. Storage areas should be equipped with appropriate fire - suppression systems, and access to such areas should be restricted to trained personnel only.Storage areas should have appropriate fire-suppression systems and only trained personnel should be allowed access.

Thirdly, the container used for storage is crucial.Thirdly, it is important to have a container that can be used for storage. It should be made of a material that is compatible with 2,2,3,3 - tetrafluoropropyl methacrylate.It should be made from a material compatible with 2,2,3,3-tetrafluoropropylmethacrylate. Glass or certain types of high - density plastics are often good choices.Glass or certain types high-density plastics are good choices. The container should be tightly sealed to prevent evaporation of the compound, as well as to avoid contact with air and moisture.The container must be tightly sealed in order to prevent evaporation and to avoid contact with moisture and air. Exposure to air can lead to oxidation, while moisture can initiate hydrolysis reactions, both of which can degrade the quality of the chemical.Moisture and air exposure can cause oxidation. Both can affect the quality of a chemical.

Fourthly, it is important to store this compound away from reactive substances.It is important to keep this compound away form reactive substances. It may react with strong acids, bases, or oxidizing agents.It can react with strong bases, acids, or oxidizing agents. For example, an oxidizing agent could cause an oxidation reaction that changes the chemical structure of 2,2,3,3 - tetrafluoropropyl methacrylate.An oxidizing agent, for example, could cause an oxidation that changes the chemical composition of 2,2,3,3-tetrafluoropropylmethacrylate. When storing in a shared storage area, ensure proper segregation based on the reactivity of different chemicals.If you are storing chemicals in a shared area, make sure to segregate them according to their reactivity.

Finally, proper labeling of the storage container is essential.Labeling the container properly is also essential. The label should clearly indicate the name of the compound, its chemical formula, any hazard warnings such as flammability or reactivity, and the date of storage.Labels should clearly state the name of the chemical, its chemical formula and any warnings about hazards such as flammability, reactivity or reactivity. They should also include the date of storage. This helps in easy identification, traceability, and safe handling of the chemical during its storage period.This allows for easy identification, traceability and safe handling during the storage period.