Chemical Formula | BF3·CH3OH |
Molecular Weight | 104.85 g/mol |
Appearance | Colorless to pale yellow liquid |
Odor | Pungent odor |
Density | 1.276 g/mL at 25 °C |
Boiling Point | 59 - 62 °C |
Melting Point | -42.5 °C |
Solubility | Soluble in methanol, ethanol, and other organic solvents |
Vapor Pressure | 13.3 kPa at 24.5 °C |
Flash Point | Non - flammable |
What are the main uses of Boron Trifluoride Methanol?
Boron (Boron), boron trifluoride (Trifluoride) and methanol (Methanol) are widely used.
In the field of organic synthesis, it is often used as a catalyst. Boron trifluoride-methanol complexes can assist in many reactions, such as esterification reactions. In such reactions, it can effectively increase the reaction rate, so that alcohols and carboxylic acids can be converted into esters more efficiently, which is crucial in the preparation of fine chemicals such as fragrances and pharmaceuticals.
also plays a key role in the etherification reaction. It can promote the dehydration of alcohol molecules to form ethers, or the etherification of alcohols and olefins, providing a variety of ether products for organic synthesis and enriching the types of organic compounds.
In the field of carbohydrate chemistry, boron trifluoride methanol is often used for the methylation analysis of sugars. After this treatment, sugar molecules are methylated at specific locations. Subsequent analysis methods such as mass spectrometry can clarify the structural information of sugars, which is of great significance for the study of sugar compounds.
In addition, in some subsequent processing steps of borohydride reactions, boron, boron trifluoride, and methanol systems may also participate in them, modifying and transforming the reaction products, further expanding the path of organic synthesis, and providing assistance for the acquisition of organic compounds with different structures and properties.
What are the storage conditions for Boron Trifluoride Methanol?
Boron (Boron), boron trifluoride (Trifluoride) and methanol (Methanol), its storage conditions are quite important. Boron is more active and easily reacts with water vapor and oxygen in the air. Boron trifluoride will hydrolyze rapidly in contact with water, and methanol is a volatile and flammable liquid.
Therefore, store the mixture of these three in a dry environment. It should be placed in a closed container to prevent water vapor in the air from invading, causing boron trifluoride to hydrolyze and affecting the properties of the mixture. The material of the container should also be carefully selected, and it should be corrosion-resistant. Because boron trifluoride is corrosive, it can erode some common materials.
Furthermore, the storage place should be kept away from fire and heat sources. Methanol is flammable, and it is very easy to burn and explode in case of open flames and hot topics, and its steam and air can form explosive mixtures. At the same time, the temperature should also be properly controlled and not too high to prevent excessive volatilization of methanol or other chemical reactions.
In addition, the storage place should be well ventilated. If methanol evaporates, it can be discharged in time to reduce the concentration of combustible steam in the air and reduce the risk of explosion. And clear warning signs should be set up to inform the danger of this mixture, so that relevant personnel can treat it with caution. In this way, the mixture of boron, boron trifluoride and methanol must be properly stored to ensure safety.
What safety precautions should be paid attention to when using Boron Trifluoride Methanol
The mixed reagent composed of boron (Boron), boron trifluoride (Trifluoride) and methanol (Methanol), when using, many safety matters must be observed.
First of all, it should be noted that this mixed reagent is corrosive. Boron trifluoride generates highly corrosive hydrofluoric acid in contact with water, which can erode the skin and respiratory tract. Therefore, when operating, it is necessary to wear complete protective equipment, such as acid and alkali-resistant gloves, protective glasses and protective clothing, to prevent the reagent from contacting the body. If you accidentally touch it, you should quickly rinse it with a lot of water and seek medical attention immediately.
Secondly, methanol is toxic. Although it plays a key role in mixed reagents, its volatile gas can enter the body through the respiratory tract, causing dizziness, fatigue, blurred vision and other poisoning symptoms. The operation should be carried out in a well-ventilated place, preferably in a fume hood, to reduce the risk of methanol vapor inhalation.
Furthermore, this mixture of reagents is sensitive to heat. If it is heated or exposed to an open flame, it may react violently or even explode. Therefore, it should be kept away from heat sources and open flames and stored in a cool, dry and well-ventilated place. Avoid using overheated appliances during operation to prevent danger.
In addition, boron trifluoride is a suffocating gas. Use in a limited space, or due to gas accumulation, the oxygen content will be reduced, leading to the risk of suffocation. Therefore, the place of use needs to have a good ventilation system to ensure air circulation. < Br >
Using boron, boron trifluoride and methanol mixed reagents, every step must be carefully followed, and safety procedures must be strictly followed to ensure experimental safety and personnel well-being.
What are the physical and chemical properties of Boron Trifluoride Methanol
Boron (Boron), boron trifluoride (Trifluoride) and methanol (Methanol) constitute a system whose physicochemical properties are particularly important. Boron, hard and brittle, is a black or silver-gray solid with active chemical properties and is often used as a semiconductor material. Boron trifluoride, a highly corrosive colorless gas, reacts violently in contact with water and is a commonly used catalyst in organic synthesis. Methanol, a volatile and flammable colorless liquid, is an important organic raw material and solvent.
When boron, boron trifluoride and methanol coexist, boron trifluoride can react with methanol. The strong Lewis acidity of boron trifluoride can form coordination bonds with the oxygen atoms of methanol to form complexes. In the field of organic synthesis, this complex is often used as a high-efficiency catalyst for esterification and etherification reactions.
From the perspective of physical properties, the boiling point, density and other properties of the system will change due to the reaction of boron trifluoride with methanol. Although boron does not directly react with methanol or boron trifluoride, its presence may affect the physical properties and reactivity of the system. For example, the surface properties of boron can adsorb the reactants and change the reaction rate.
Chemically, this system exhibits unique activity in organic synthesis. In the esterification reaction, it can accelerate the reaction process of alcohol and carboxylic acid and increase the yield of esters. In the etherification reaction, it can also promote the dehydration of alcohol molecules to ether. However, due to the strong corrosiveness and toxicity of boron trifluoride, extra caution must be taken during operation, protective measures must be taken, and the waste after the reaction must be properly disposed of to prevent environmental pollution and human harm.
What is Boron Trifluoride Methanol?
The preparation method of boron trifluoride methanol, although the ancient book "Tiangong Kaiwu" does not contain this substance, it can be described as follows in terms of chemical understanding.
First, to prepare boron trifluoride methanol, prepare boron sources first, such as borax (Na ² B O · 10H ² O). Borax is dissolved in water and treated with sulfuric acid to obtain boric acid (H 🥰 BO 🥰). The reaction formula is as follows: Na ² B O · 10H ² O + H ² SO → 4H 🥰 BO 🥰 + Na ² SO + 5H ² O.
times, boric acid is co-heated with fluorite (CaF ²) and concentrated sulfuric acid to prepare boron trifluoride. This reaction needs to be carried out in a special corrosion-resistant container, because strong corrosive substances are involved in the process. The reaction formula is: H < BO < 3CaF < 3H < SO > → BF < Br > + 3CaSO < 3H < O >. The resulting boron trifluoride gas is dried and removed for later use.
Finally, the obtained dry boron trifluoride gas is passed into anhydrous methanol. The methanol needs to be dehydrated in advance to maintain the purity of the product. Boron trifluoride and methanol can form a stable complex, namely boron trifluoride methanol. This process requires temperature control to prevent overreaction.
When preparing, it is necessary to abide by the chemical operation specifications, because the raw materials used are corrosive, toxic, and the reaction conditions are harsh. Although this detailed method is not covered in Tiangong Kaiwu, a complete preparation method can be obtained according to chemical principles and modern technology.