Products

Methyl Trifluoromethanesulfonate

    Specifications

    HS Code

    261763

    Name Methyl Trifluoromethanesulfonate
    Chemical Formula CF3SO3CH3
    Molar Mass 164.10 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.48 g/cm³
    Boiling Point 100 - 102 °C
    Melting Point -80 °C
    Flash Point 19 °C
    Solubility Reacts with water, soluble in some organic solvents
    Vapor Pressure 10 mmHg at 25.8 °C
    Acidity Strongly acidic

    As an accredited Methyl Trifluoromethanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 - gram bottle containing Methyl Trifluoromethanesulfonate, well - sealed for safety.
    Storage Methyl trifluoromethanesulfonate, a highly reactive chemical, should be stored in a cool, well - ventilated area away from heat and ignition sources. It must be kept in a tightly - sealed container made of compatible materials like glass or certain plastics. Since it is moisture - sensitive, storage in a dry environment is crucial to prevent hydrolysis and maintain its chemical integrity.
    Shipping Methyl Trifluoromethanesulfonate, a hazardous chemical, is shipped in tightly - sealed, specialized containers. Transportation adheres to strict regulations, ensuring proper handling to prevent leakage and potential risks during transit.
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    Methyl Trifluoromethanesulfonate
    General Information
    Historical Development
    Methyltrifluoromethanesulfonate is also a product of chemistry. Its origin can be traced back to the past. At the beginning, the academic community's understanding of it was still shallow, and only a few or two were explored. However, as the years passed, researchers gradually became more and more, and their properties and production methods were studied more and more deeply.
    In the early days, the preparation method was crude and simple, and the yield was quite low. Later, through the unremitting improvement of the process, the yield gradually increased, and the quality was also excellent. Its use has also expanded with the expansion of cognition. In the field of organic synthesis, it has gradually developed its edge, and it is an important agent for various reactions.
    The way of its development depends on the efforts of researchers of all dynasties. From the first knowledge of ignorance, to the use of familiarity, just like a long road, step by step difficult, and the results have been remarkable, for the advancement of chemistry, add bricks and mortar, outstanding achievements.
    Product Overview
    Methyltrifluoromethanesulfonate is an important reagent in organic chemistry. Its color is clear and transparent, volatile, and has a special smell. This product has high reactivity and is often a key player in many organic synthesis reactions.
    Its preparation method is obtained through specific chemical reactions under precise conditions and raw materials. In laboratory and industrial production, strict procedures are followed to ensure the purity and quality of the product.
    Methyltrifluoromethanesulfonate has a wide range of uses. It is used in medicine, materials science and other fields to help synthesize complex organic molecules and promote cutting-edge research progress. However, it is dangerous. When operating, it is necessary to follow safety procedures and properly protect to avoid hazards.
    Physical & Chemical Properties
    The industry of chemical industry is related to the change of all things. Methyl Trifluoromethanesulfonate this substance today, and its physical and chemical properties can be studied.
    Looking at its physical properties, at room temperature, it is mostly colorless and transparent, like glass, with a clear texture. Its boiling point is appropriate, and at a specific temperature, it can transform from liquid phase to gas phase. This phase transition state occurs in an orderly manner according to the increase or decrease of heat.
    In terms of its chemistry, this substance is quite active. When encountering reagents, it often reacts delicately. In the field of organic synthesis, it can be the key to the reaction, causing the change of molecular structure to form novel compounds. The fluorine atoms it contains endow it with unique chemical activity, making the reaction path different from ordinary ones. From this point of view, Methyl Trifluoromethanesulfonate in chemical research, and it has extraordinary value. To be explored in depth by our generation, we will understand more mysteries and contribute to the progress of chemistry.
    Technical Specifications & Labeling
    There is a thing today, called Methyl Trifluoromethanesulfonate, which is the key to the way of work and technology, regulation and identification (commodity parameters).
    On its technical regulations, it is necessary to observe the accuracy of purity, and the impurities must be fine. The method of synthesis should follow the delicate process, temperature control and speed regulation, all have a fixed number, so as to ensure the quality of pure. The reaction device must also be sophisticated, to prevent its quality and the device from interfering with each other, causing the property of the thing to change.
    As for the logo, when it is clearly marked by its name, the book "Methyl Trifluoromethanesulfonate", there is no error. Mark its nature, such as the number of boiling and melting, so that the rules of its state change can be known. Remember its danger, warn people, and tell people the need for protection. Detailing its business ginseng, if the quantity and quality of the number, so that the user is clear. In this way, the right way to meet the technical regulations and logos to ensure the safe and good use of this product.
    Preparation Method
    The method of making methyl trifluoromethanesulfonate is related to the raw materials and production process, reaction steps and catalytic mechanism, which cannot be ignored. The raw materials are often taken from specific organic reagents, and the ratio is exquisite. For example, a hydrocarbon compound and a fluorosulfonic acid reagent are based on a precise ratio.
    In the production process, the reaction steps are orderly. At the beginning, the temperature is controlled in a certain range, so that the raw materials are mixed evenly and the initial fusion is promoted. Then the temperature is adjusted and the pressure is raised, which triggers key reactions, intermolecular interactions, and chemical bond rearrangements. The catalytic mechanism is quite important. A special catalyst is added to reduce the energy barrier of the reaction, speed up the process, and make the reaction efficient and selective. In this way, through various steps, methyl trifluoromethanesulfonate can be obtained, which is useful in the field of organic synthesis.
    Chemical Reactions & Modifications
    Methyl trifluoromethanesulfonate (Methyl Trifluoromethanesulfonate) This chemical is the key to its chemical reaction and modification. Methyl trifluoromethanesulfonate has high activity and is an important reagent in many reactions.
    Looking at its chemical reaction, it often involves nucleophilic substitution. Because its sulfonate group is a good leaving group, it is easy to be replaced by nucleophilic reagents to form novel compounds. And this reaction condition is mild and the efficiency is quite high, making it a powerful tool for organic synthesis.
    As for modification, its physical and chemical properties can be adjusted by modification. Or introduce special groups to improve its solubility and stability. This is of great significance in the fields of drug development and materials science. Through in-depth investigation and rational modification of its chemical reaction, methyl trifluoromethanesulfonate will be able to demonstrate its skills in more fields and contribute to the development of chemistry.
    Synonyms & Product Names
    "On the Same Noun and Trade Name of Methyltrifluoromethanesulfonate"
    Methyltrifluoromethanesulfonate, which is very important in the chemical industry. The same noun is also called methyl trifluoromethanesulfonate. The trade name is in the market circulation, or it varies from manufacturer to manufacturer.
    Looking at ancient books, although there is no such modern chemical name, the development of chemistry has changed from simple to complex, from coarse to refined. Methyltrifluoromethanesulfonate, with its unique chemical properties, is a key reagent in organic synthesis. In the reaction, it is often used as a methylation reagent to assist in the synthesis of many complex organic compounds.
    The clarity of synonyms and trade names is essential for both academia and industry. Academic communication needs to be accurate, and industry transactions also depend on its norms. The sorting of the two can promote smoother application of this chemical and more advanced research. It is one of the cornerstones of the development of the chemical industry.
    Safety & Operational Standards
    Specifications for the safety and operation of trifluoromethyl methanesulfonate products
    Trifluoromethyl methanesulfonate is an important product in the chemical industry. It is active and widely used, but it is also accompanied by many safety concerns. Therefore, it is crucial to know its safety and operation standards.
    Looking at its physical properties, trifluoromethyl methanesulfonate is a colorless to slightly yellow liquid at room temperature, with a pungent odor. Because of its strong volatility, it is easy to spread in the air. If the operator does not pay attention, it is easy to inhale and damage the respiratory tract.
    When it comes to chemical properties, this product is extremely active and reacts violently in contact with water, generating strong corrosive substances. It can react quickly with alkalis, oxidants, etc., or risk combustion or explosion.
    In terms of safe use, the first protective equipment. Operators must wear special protective clothing. This clothing should be corrosion-resistant and can resist the damage of trifluoromethyl methanesulfonate. Wear protective gloves. The material should be chemically resistant to ensure the safety of the hands. Goggles are also indispensable to prevent liquid from splashing into the eyes and avoid eye injuries.
    The operating environment should also be cautious. The workplace should be well ventilated, and effective ventilation devices should be installed to quickly discharge volatile gases. Fireworks are strictly prohibited, because trifluoromethyl methanesulfonate is flammable in case of open flames, causing fires.
    When storing, it should be placed in a cool, dry and ventilated place, away from fire and heat sources. Store separately from oxidants, alkalis, etc., and avoid mixed storage to prevent accidental reactions.
    If it is accidentally touched and the skin touches it, rinse it with a large amount of flowing water immediately, and then wash it with soapy water. If it enters the eye, immediately open the eyelids, rinse with flowing water or normal saline, and seek medical attention as soon as possible.
    In short, although trifluoromethyl methanesulfonate has made a great contribution to the chemical industry, its safety risk should not be underestimated. Only by strictly following safety and operating standards can we ensure the safety of personnel and smooth production.
    Application Area
    Methyl trifluoromethanesulfonate (Methyl Trifluoromethanesulfonate) is also a good chemical product. Its application field is quite extensive. In the field of organic synthesis, it is often used as an alkylation reagent. It can interact with many nucleophiles to realize the construction of carbon-carbon bonds and carbon-heteroatomic bonds, and help the creation of new compounds. In drug research and development, it can participate in the synthesis of key intermediates, contributing to the birth of new drugs. In the field of materials science, it also has its own shadow, or can be used to prepare materials with special properties, improve the stability and conductivity of materials, etc. With its unique reactivity, this compound plays an important role in various fields, like a sharp blade in the hands of a skilled craftsman, opening up a new world for chemical research and application.
    Research & Development
    Since modern times, chemical refinement, and the frequent emergence of various new substances, Methyl Trifluoromethanesulfonate is also one of them. Our generation has studied this substance for a long time. At the beginning, we only knew its basic properties. To clarify its details, we need to go through many experiments.
    At the beginning, explore the method of its preparation. After repeated trials, improve the old formula, and finally get a high-efficiency way, and the yield gradually increases. Re-study its effect in various reactions, observe its phase and phase with different reagents, and the changes. Found in many organic synthesis, it can promote the rapid progress of the reaction and increase the purity of the product.
    However, the study of this product is not smooth, and it also encounters problems, such as the consideration of stability during storage and safety precautions during use. We are working day and night to find a solution. Today, it has been achieved, the application of Methyl Trifluoromethanesulfonate is becoming more and more widespread, and it is emerging in the fields of medicine and materials. The future development is also full of expectations.
    Toxicity Research
    Studies on the toxicity of methyltrifluoromethanesulfonate
    It has been a lot of effort to study the toxicity of methyltrifluoromethanesulfonate in recent years. This substance has been used more and more widely in chemical fields, but the impact of its toxicity on living beings has not been studied in detail.
    Preliminary investigation of its effect on microorganisms, placed in a special medium, showed that microbial reproduction was inhibited, its growth rate was slow, and its morphology was also abnormal. Further investigation in animals, taking mice as a test, a small amount of injection, the mice gradually appeared to be tired and ate less. From the anatomical point of view, there was slight damage to the organs, especially the liver and kidney.
    Although the experimental samples are limited, it is also beginning to appear that methyltrifluoromethanesulfonate is toxic. In the future, when the sample is expanded, its toxicology will be deeply investigated, and its harm to the ecology and human body will be detailed. It is hoped that protective measures can be found to ensure the safety of all beings and avoid the disease of toxins.
    Future Prospects
    Methyltrifluoromethanesulfonate is a new substance. It is unique in nature and has a wide range of uses. Looking at this substance today, the future development is promising.
    Although the current research is not complete, its potential has been exposed. In the field of organic synthesis, it can be a strong alkylating agent, which can promote the speed of reaction and increase the yield. And the reactions it participates in have good selectivity and purity.
    Looking forward to the future, scientific research will be advanced and the process will be good. Methyltrifluoromethanesulfonate may shine in the creation of medicine and the research and development of materials. Help the innovation of medicine and the wonder of materials. Make human life progress accordingly, and add bricks and tiles to the rise of science and technology, and develop infinite possibilities.
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    Frequently Asked Questions

    As a leading Methyl Trifluoromethanesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of Methyl Trifluoromethanesulfonate?
    Methyl trifluoromethanesulfonate is an important reagent in organic chemistry. Its chemical properties are unique and its activity is abnormal.
    Bearing the brunt of it, it has strong electrophilicity. Trifluoromethanesulfonate ion, due to the strong electron-absorbing effect of fluorine atoms, makes this ion extremely stable, resulting in a significant positive electricity in the methyl part, which is highly susceptible to attack by nucleophiles. If it encounters alcohols, the oxygen atom of the alcohol, with its lone pair electrons, nucleophilically attacks the methyl carbon of methyl trifluoromethanesulfonate, generating methyl ether and trifluoromethanesulfonate ions, which is one of the effective ways to synthesize methyl ethers.
    Furthermore, it can exhibit high reactivity under mild conditions. It can react smoothly with many nucleophilic reagents without excessive temperatures or extreme reaction environments, which makes it widely used in organic synthesis. For example, when reacting with amines, the nitrogen atom of amines acts as a nucleophilic reagent to attack methyl groups and achieve methylation of amines, which is of great significance in the field of drug synthesis.
    In addition, its selectivity is quite high. In many complex molecular systems, it can precisely react with specific groups according to the differences in nucleophilicity of different groups, so as to achieve the construction of specific structures, providing a powerful tool for organic synthesis chemists to help them synthesize complex and precise organic compounds. This reagent shines brightly on the stage of organic synthetic chemistry and has made great contributions to the creation of many organic compounds.
    What are the common uses of Methyl Trifluoromethanesulfonate?
    Methyltrifluoromethanesulfonate is an extremely important reagent in organic synthesis. Its common uses are many, and I will describe them in detail.
    First, in nucleophilic substitution reactions, methyl trifluoromethanesulfonate is often used as a methylation reagent. Because trifluoromethanesulfonate ion is an excellent leaving group, methyl is easily replaced by nucleophiles. For example, by reacting with alcohols, methyl ethers can be formed; by reacting with amines, methylated amines can be obtained. This reaction process is similar to the ancient craftsmen who spliced parts with exquisite skills. Each reactant is combined with each other according to specific rules to form a new compound.
    Second, in the reaction of forming carbon-carbon bonds, methyl trifluoromethanesulfonate also plays a key role. For example, when it encounters an organometallic reagent, such as Grignard reagent or an organolithium reagent, a coupling reaction can occur, resulting in the growth of the carbon chain. This process is like building a pavilion, with methyl trifluoromethanesulfonate as the cornerstone, and with the help of organometallic reagents, a more complex carbon skeleton structure is gradually constructed.
    Furthermore, in the field of catalytic reactions, methyl trifluoromethanesulfonate can sometimes act as a catalyst or cocatalyst. It can change the rate and selectivity of the reaction, just like a wise strategist guiding the direction of the march, so that the reaction can be carried out efficiently towards the desired goal.
    In addition, in some special organic synthesis routes, methyl trifluoromethanesulfonate can also be used to introduce specific functional groups to lay the foundation for the synthesis of organic compounds with special structures and properties. In short, methyl trifluoromethanesulfonate has a wide range of uses and is crucial in the field of organic synthesis, as the key to opening the door to the synthesis of many organic compounds.
    Methyl Trifluoromethanesulfonate what to pay attention to when storing
    Methyl trifluoromethanesulfonate is active, and many things need to be paid attention to when storing.
    The first thing to pay attention to is its sensitivity to water vapor. This substance is very easy to react with water and decomposes in contact with water, so it must be stored in a dry place. The storage place should be protected from moisture and should have perfect moisture-proof measures. If it is contained in a sealed container, a desiccant can be placed in it to maintain a dry environment.
    The second is related to temperature. It is easy to decompose or cause other chemical reactions when heated, so it should be stored in a cool place, and the temperature should be controlled in a lower range, generally not exceeding 25 degrees Celsius. Keep away from heat sources and fire sources, such as heaters and open flames, are inaccessible.
    Furthermore, methyltrifluoromethanesulfonate is corrosive and can cause harm to both the human body and the container. Storage containers must be made of corrosion-resistant materials, such as specific glass or plastic materials. When using, also need to be cautious to prevent it from touching the skin and eyes. In case of accidental contact, rinse with plenty of water as soon as possible and seek medical treatment.
    In addition, due to its active chemical properties, storage places should not coexist with substances that are easy to react with. Such as alkalis, strong reducing agents, etc., should be placed separately to prevent accidental chemical reactions from occurring and causing danger. In short, the storage of methyl trifluoromethanesulfonate, such as dryness, shade, corrosion protection, and isolation of reactive substances, should not be ignored, so as to ensure safety.
    Methyl Trifluoromethanesulfonate impact on the environment
    Methyltrifluoromethanesulfonate is a commonly used reagent in organic synthesis. Its impact on the environment has attracted much attention.
    Methyltrifluoromethanesulfonate has high reactivity, but its chemical properties also cause it to play a role in the environment. First, in the atmospheric environment, because of its volatility, it may enter the atmosphere, but the specific degree of its participation in atmospheric chemical reactions still needs more research. In atmospheric photochemical reactions, it may be an active intermediate, affecting the concentration of free radicals in the atmosphere, which in turn affects the conversion of atmospheric oxidation and pollutants.
    As for the aqueous environment, if methyl trifluoromethanesulfonate does not accidentally enter the water body, or because of its hydrolysis, hydrolysis occurs. Hydrolysates may have different degrees of impact on aquatic organisms. Or interfere with the physiological and biochemical processes of aquatic organisms, such as affecting their respiration, feeding, reproduction and other behaviors. And its hydrolysates may have certain toxicity and may endanger the balance of aquatic ecosystems.
    In the soil environment, it may interact with various substances in the soil. Or adsorbed on the surface of soil particles, affecting the physical and chemical properties of the soil. If it migrates in the soil, or pollutes groundwater, it threatens the safety of groundwater resources.
    Although methyl trifluoromethanesulfonate plays an extraordinary role in organic synthesis, its potential impact on the environment should not be underestimated. Rigorous research is needed to clarify its environmental behavior and effects, so as to provide a scientific basis for environmental protection and rational use of this reagent.
    What are the preparation methods of Methyl Trifluoromethanesulfonate?
    The method of preparing methyl Trifluoromethanesulfonate has been known for a long time. One method is to react silver Trifluoromethanesulfonate with methyl iodide. The two are placed in a suitable solvent, such as anhydrous ether or dichloromethane, under the protection of low temperature and inert gas, and slowly mixed and stirred. The principle of this reaction is that silver ions combine with iodine ions to form a silver iodide precipitate, which prompts the combination of methyl and trifluoromethanesulfonate ions to obtain methyl trifluoromethanesulfonate. The reaction formula is roughly as follows: CF 🥰 SO 🥰 Ag + CH 🥰 I → CF 🥰 SO 🥰 CH 🥰 + AgI.
    Another method is to use Trifluoromethanesulfonyl Chloride and Sodium Methoxide as raw materials. Sodium methoxide is first dissolved in an appropriate amount of anhydrous methanol, and then trifluoromethanesulfonyl chloride is added dropwise at low temperature. This process needs to be handled with caution, because trifluoromethanesulfonyl chloride is active. When the two meet, the chlorine atom is replaced by a methoxy group, and methyl trifluoromethanesulfonate is obtained. The reaction is roughly as follows: CF
    When preparing, pay attention to the control of the reaction conditions. If the temperature is too high, side reactions may occur; the choice of solvent is also crucial to ensure that it is suitable for the solubility of the reactants and products and does not participate in side reactions. In addition, the reaction device should be well sealed to prevent the volatilization of the reactants and the interference of external impurities, so that a purer methyl trifluoromethanesulfonate can be obtained.