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Methacrylic Acid 2,2,3,3,4,4,5,5-octafluoropentyl Ester~1h,1h,5h-perfluoro-1-pentyl Methacrylate


Properties
Product Name Methacrylic acid 2,2,3,3,4,4,5,5-octafluoropentyl ester
Cas Number 355-93-1
Formula C9H8F8O2
Molar Mass 322.15 g/mol
Boiling Point 149-150°C
Density 1.532 g/cm3
Refractive Index 1.338
Flash Point >100°C
Viscosity Not available
Vapor Pressure 1.5 mmHg at 25°C
Pka Not available
Solubility In Water Insoluble
Appearance Clear liquid
Odor Mild
Autoignition Temperature Not available
FAQ

What is the CAS number of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5-octafluoropentyl ester~1H,1H,5H-Perfluoro-1-pentyl methacrylate?

The CAS number for Methacrylic acid 2,2,3,3,4,4,5,5 - octafluoropentyl ester or 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate is 1996 - 88 - 9.The CAS number of Methacrylic Acid 2,2,3,3,4,4,5 - octafluoropentyl ester or 1H1,1H5H – Perfluoro-1 - pentylmethacrylate is 1997 - 88-9.
This compound is an ester formed from methacrylic acid and a perfluorinated alcohol.This compound is an ester formed from methacrylic and perfluorinated alcohol. Esters are important in various industries.Esters are used in many industries. In the case of this particular perfluoroalkyl - containing ester, it has properties influenced by both the methacrylic acid moiety and the perfluorinated pentyl group.This particular perfluoroalkyl-containing ester has properties that are influenced by the methacrylic and perfluorinated pentyl groups.

The methacrylic acid part provides the potential for polymerization due to the presence of the carbon - carbon double bond.The double carbon-carbon bond in the methacrylic part of the acid provides the potential for polymerization. This allows it to be incorporated into polymers, which can be used in applications such as coatings, adhesives, and dental materials.This allows it be incorporated into polymers that can be used for applications such as dental materials, adhesives and coatings. The perfluorinated pentyl group imparts unique characteristics.The perfluorinated group confers unique properties. Perfluorinated groups are known for their hydrophobic and oleophobic properties, meaning they repel both water and oils.The hydrophobic and oil-repelling properties of perfluorinated groups make them a popular choice.

This combination of properties makes the 2,2,3,3,4,4,5,5 - octafluoropentyl methacrylate useful in applications where a polymer needs to have both good mechanical properties from the methacrylic backbone and the surface - active properties from the perfluorinated side - chain.This combination of properties makes 2,2,3,3,4,4,5 - octafluoropentyl - methacrylate useful for applications where a material needs to have good mechanical properties due to the methacrylic side-chain and surface-active properties due the perfluorinated chain. For example, in fabric coatings, it can help make the fabric resistant to stains and water penetration.In fabric coatings, for example, it can make the fabric resistant against stains and water. In the dental field, it may be used in composites to improve their resistance to moisture and enhance their durability.In the dental industry, it can be used to improve composites' resistance to moisture and durability. Overall, its CAS number is a crucial identifier for researchers, manufacturers, and regulatory bodies when dealing with this specific chemical compound in various scientific and industrial contexts.Its CAS number is an important identifier when it comes to dealing with this chemical compound in different scientific and industrial contexts.

What are the applications of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5-octafluoropentyl ester~1H,1H,5H-Perfluoro-1-pentyl methacrylate?

Methacrylic acid 2,2,3,3,4,4,5,5 - octafluoropentyl ester or 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate has several important applications.There are many important applications for methacrylic acid 2,2,3,3,4,4,5 - octafluoropentyl ester or 1H1,1H,5H-Perfluoro- 1- pentylmethacrylate.
In the field of coatings, it is highly valued.It is highly valued in the field of coatings. The presence of the fluorinated alkyl chain in this compound imparts unique surface - modifying properties.This compound has unique surface-modifying properties due to the presence of fluorinated alkyl chains. Coatings formulated with this ester can have enhanced water - repellency, oil - repellency, and stain - resistance.Coatings formulated using this ester have improved water - and oil-repellency, as well as stain-resistance. For example, in architectural coatings, it can help protect building exteriors from environmental factors such as rain, dirt, and oil splashes.In architectural coatings it can protect the exteriors of buildings from environmental factors like rain, dirt and oil splashes. The fluorinated groups reduce the surface energy of the coating, causing water and oil to bead up and roll off easily.The fluorinated groups decrease the surface energy of coatings, causing oil and water to bead and roll off easily.

In the production of specialty polymers, this methacrylate ester is a key monomer.This methacrylate ester plays a major role in the production of specialty plastics. When polymerized, it can form polymers with excellent chemical resistance.It can be polymerized to form polymers that are highly resistant to chemicals. These polymers are suitable for applications where exposure to harsh chemicals is a concern, such as in chemical storage tanks or industrial pipelines.These polymers can be used in applications where harsh chemicals are present, such as chemical storage tanks and industrial pipelines. The fluorinated side chains act as a shield, preventing the penetration of various chemical substances into the polymer matrix.The fluorinated chains act as a barrier, preventing chemical substances from penetrating the polymer matrix.

It also has applications in the electronics industry.It is also used in the electronics industry. In the manufacturing of printed circuit boards (PCBs), the low - surface - energy polymers derived from this ester can be used for coating components.The low-surface-energy polymers derived by this ester are used to coat components in the manufacture of printed circuit boards. This helps to prevent the adhesion of dust, moisture, and other contaminants, which could potentially disrupt the electrical performance of the PCB.This helps prevent the adhesion and contamination of dust, moisture and other contaminants that could disrupt the electrical performance. Additionally, in the production of liquid crystal displays (LCDs), it can be used in the synthesis of polymers for alignment layers.In addition, it can also be used to synthesize polymers for the alignment layers in liquid crystal displays. The unique properties of the fluorinated polymer can assist in controlling the orientation of liquid crystal molecules, improving the display quality.The fluorinated polymer's unique properties can help control the orientation of liquid-crystal molecules, improving display quality.

In the biomedical field, it has potential uses.It has potential applications in the biomedical sector. For instance, in the development of medical device coatings.In the development of medical devices coatings, for example. The water - and protein - resistant properties of polymers made from this ester can prevent the adhesion of biological substances like proteins and cells to the surface of medical devices.Polymers made from this ester have water- and protein-resistant properties that can prevent biological substances such as proteins and cells from adhering to the surface of medical device. This can reduce the risk of biofouling and subsequent infections, making it useful for applications such as catheters and implantable devices.This reduces the risk of biofouling, and subsequent infections. It is therefore useful for applications like catheters and implantable medical devices.

Overall, methacrylic acid 2,2,3,3,4,4,5,5 - octafluoropentyl ester plays a significant role in a wide range of industries, leveraging its fluorine - related properties to provide enhanced performance and functionality.Overall, methacrylic acids 2,2,3,3,4,4,5 - octafluoropentyl esters play a significant role across a range of industries. They leverage their fluorine-related properties to enhance performance and functionality.

What is the purity of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5-octafluoropentyl ester~1H,1H,5H-Perfluoro-1-pentyl methacrylate?

The question asks about the purity of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5 - octafluoropentyl ester or 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate. However, the provided information does not directly give the purity value.The information provided does not directly provide the purity value.
Typically, the purity of a chemical compound can be determined through various analytical methods.Analytical methods can usually be used to determine the purity of a chemistry compound. One common approach is gas chromatography (GC).Gas chromatography is a common method. In GC, the sample is vaporized and carried by an inert gas through a column.In GC, a sample is vaporized by an inert and carried through a column using an inert gas. Different components in the sample will interact differently with the column's stationary phase, leading to separation based on their physical and chemical properties.The stationary phase of the column will react differently with different components in the sample, resulting in separation based on physical and chemical properties. The detector at the end of the column then measures the amount of each component, and the purity can be calculated as the percentage of the target compound relative to all the detected components.The detector at each end of the column measures the amount of every component. The purity can then be calculated by dividing the target compound by all detected components.

Another method is high - performance liquid chromatography (HPLC).HPLC is another method. Similar to GC, HPLC separates components in a liquid sample.HPLC is similar to GC in that it separates components from a liquid sample. It is especially useful for compounds that are not volatile or are thermally unstable.It is particularly useful for compounds that do not have a volatile nature or are thermally instabile. By comparing the peak area of the target compound with the total peak area of all peaks in the chromatogram, the purity can be estimated.Purity can be estimated by comparing the peak areas of the target compound and the total peak areas of all peaks on the chromatogram.

Nuclear magnetic resonance (NMR) spectroscopy can also provide information about purity.NMR spectroscopy is also a way to determine purity. Impurities can sometimes be detected as additional signals in the NMR spectrum.Sometimes, impurities are detected as additional signals within the NMR spectrum. By analyzing the intensities of the signals corresponding to the target compound and any potential impurities, an estimate of purity can be made.Purity can be estimated by analyzing the intensities and frequencies of the signals that correspond to the target compound, as well as any potential impurities.

Without any experimental data or a stated value from the source where this compound was obtained, it's impossible to accurately state the purity.It is impossible to accurately determine the purity of a compound without any experimental data, or a value stated by the source from which it was obtained. If this compound was purchased from a chemical supplier, the purity should be specified on the product label or in the accompanying documentation.If the compound was purchased from an approved chemical supplier, it should be stated on the label or accompanying documentation. If it was synthesized in - house, the purity would need to be determined using one of the above - mentioned analytical techniques.If the compound was synthesized at home, the purity should be determined by using one of the analytical techniques mentioned above.

In conclusion, based on the information given in the question, the purity of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5 - octafluoropentyl ester or 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate cannot be determined. Appropriate analytical methods need to be employed to measure its purity accurately.To accurately measure its purity, it is necessary to use appropriate analytical methods.

What is the stability of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5-octafluoropentyl ester~1H,1H,5H-Perfluoro-1-pentyl methacrylate?

The stability of Methacrylic acid 2,2,3,3,4,4,5,5 - octafluoropentyl ester (also known as 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate) can be considered from several aspects.You can consider the stability of Methacrylic Acid 2,2,3,3,4,4,5 - octafluoropentyl ester (also known as Perfluoro- 1 - pentyl - methacrylate 1H,1H and 5H) from different angles.
Thermal stability: This compound generally has a relatively good thermal stability.Thermal stability: This compound has a good thermal stability. The presence of the fluorinated alkyl chain and the methacrylate group contributes to its ability to withstand higher temperatures to a certain extent.The presence of a fluorinated chain and a methacrylate group helps it to withstand higher temperature to some extent. The fluorine atoms in the octafluoropentyl group have strong carbon - fluorine bonds.The fluorine in the octafluoropentyl has strong carbon-fluorine bonds. These bonds are relatively short and have high bond dissociation energies.These bonds are short and have high dissociation energies. This makes it more difficult for the molecule to break apart under thermal stress compared to non - fluorinated analogs.This makes it harder for the molecule under thermal stress to break apart compared to its non-fluorinated analogues. However, like most organic esters, at extremely high temperatures, decomposition can still occur.Decomposition is possible at high temperatures. Decomposition might involve processes such as the cleavage of the ester bond, which could lead to the formation of methacrylic acid and the fluorinated alcohol corresponding to the octafluoropentyl moiety.Decomposition can involve processes like the cleavage or ester bond which can lead to the formation methacrylic and fluorinated alcohols corresponding to octafluoropentyl.

Chemical stability: In terms of chemical reactivity, it is stable in many common non - reactive solvents.Chemical stability: It is stable in many non-reactive solvents. But it can react with strong acids, bases, and some reactive nucleophiles.It can also react with strong bases, acids and nucleophiles. For example, in the presence of strong bases, hydrolysis of the ester bond can take place.In the presence of strong base, the ester bond may be hydrolyzed. Bases can catalyze the reaction where water attacks the carbonyl carbon of the ester, ultimately leading to the formation of the carboxylate salt of methacrylic acid and the fluorinated alcohol.Bases can catalyze a reaction in which water attacks the carbonyl atom of the ester. This leads to the formation of carboxylate salts of methacrylic acids and fluorinated alcohol. With strong acids, protonation of the carbonyl oxygen of the ester can occur, which may also initiate further reactions such as esterification - type reverse reactions or other acid - catalyzed decomposition pathways.Strong acids can cause protonation of carbonyl oxygen in the ester, which can lead to further reactions, such as esterification-type reverse reactions or other acid-catalyzed pathways of decomposition.

It also has a certain degree of stability towards oxidation.It also has some stability against oxidation. The fluorinated chain provides some protection against oxidation, as fluorine is electronegative and can influence the electron density distribution in the molecule.Fluorine, which is electronegative, can affect the electron density distribution of the molecule. This provides some protection from oxidation. However, in the presence of strong oxidizing agents, such as potassium permanganate in acidic media, oxidation of the double bond in the methacrylate group or other parts of the molecule might be possible, which could lead to the formation of oxidized products like carboxylic acids or ketones.In the presence of strong oxygenating agents, such potassium permanganate, oxidation of double bonds in the methacrylate groups or other parts of a molecule may be possible. This could lead to oxidized products, like carboxylic acid or ketones.

In storage, if kept away from heat, moisture, strong acids, bases, and oxidizing agents, it can maintain its stability for an extended period.It can be stored for a long time if it is kept away from heat and moisture, strong bases, acids, and oxidizing agents. Overall, while it has good stability under normal conditions, care must be taken when handling it in environments where reactive chemicals are present.While it is stable under normal conditions, it must be handled with care in environments that contain reactive chemicals.

What is the toxicity of Methacrylic acid 2%,2%,3%,3%,4%,4%,5%,5-octafluoropentyl ester~1H,1H,5H-Perfluoro-1-pentyl methacrylate?

Methacrylic acid 2,2,3,3,4,4,5,5 - octafluoropentyl ester (also known as 1H,1H,5H - Perfluoro - 1 - pentyl methacrylate) is a fluorinated monomer.Methacrylic Acid 2,2,3,3,4,4,5 - octafluoropentyl ester (also known as Perfluoro- 1 - pentyl - methacrylate 1H,1H and 5H) is a monomer fluorinated.
Regarding its toxicity, information might be somewhat limited as it is a relatively specialized chemical.Information on its toxicity may be limited due to the fact that it is a chemical of a very specific nature. However, fluorinated organic compounds often have certain characteristics related to toxicity.Fluorinated organic chemicals often have certain characteristics that are related to their toxicity.

In general, when evaluating the toxicity of such a compound, aspects like acute toxicity need to be considered.When evaluating the toxicity, it is important to consider aspects such as acute toxicity. Acute toxicity refers to the adverse effects that occur shortly after a single exposure.Acute toxicity is the adverse effects that appear shortly after an exposure. For this ester, if it were to come into contact with the skin, it might potentially cause irritation.If this ester were to come in contact with the skin it could potentially cause irritation. The fluorinated chain could interact with the skin's lipid layers in an abnormal way, leading to redness, itching, or even more severe damage in high - dose or long - term contact scenarios.The fluorinated chains could interact abnormally with the skin's layers of lipids, causing redness, itchiness, or even more serious damage in high-dose or long-term contact scenarios.

Inhalation of its vapors could be a concern.Inhalation of the vapors is a possible concern. If the compound is in a volatile state and its vapors are inhaled, it may affect the respiratory system.Inhaling the vapors of a volatile compound could affect the respiratory system. It could potentially cause irritation to the nasal passages, throat, and lungs.It could cause irritation of the nasal passages and throat. There might be a risk of coughing, shortness of breath, or more serious respiratory problems depending on the concentration and duration of exposure.There is a risk that you might experience coughing, shortness in breath, or other respiratory problems, depending on the concentration of the substance and duration of exposure.

Oral ingestion is also a possible route of exposure.Oral exposure is another possible route. Ingesting this ester could lead to damage in the gastrointestinal tract.Ingestion of this ester may cause damage to the gastrointestinal tract. The fluorinated structure might resist normal digestion processes, and the chemical could interact with the lining of the stomach and intestines, potentially causing nausea, vomiting, abdominal pain, or more severe internal damage.The fluorinated structure could resist digestion and interact with the linings of the stomach and intestines. This could cause nausea, vomiting, abdominal discomfort, or more serious internal damage.

Long - term or chronic toxicity is another important consideration.Another important consideration is the long-term or chronic toxicity. Repeated exposure over time could potentially have cumulative effects.Repeated exposure could have cumulative effects. There is a possibility that the compound could bioaccumulate in the body, especially in fatty tissues due to its lipophilic nature.A compound's lipophilic nature could lead to bioaccumulation in the body. This is especially true in fatty tissue. This bioaccumulation might then lead to more systemic effects, such as disruption of hormonal systems or damage to vital organs like the liver and kidneys.This bioaccumulation could then lead to systemic effects such as disruptions of hormonal systems, or damage to vital organs such as the liver and kidneys. However, more research would be needed to fully understand and quantify these potential long - term toxic effects.More research is needed to fully quantify and understand these potential long-term toxic effects. Overall, while specific toxicity data may be scarce, it is reasonable to approach this compound with caution due to its fluorinated nature and potential for adverse health effects via different exposure routes.While specific toxicity data is scarce, it's reasonable to approach this compound cautiously due to its fluorinated properties and potential for adverse effects via different exposure pathways.