1 Butyl 2 Methyl Imidazole
quinoline thiophene imidazole thiazole

1-butyl-2-methyl-imidazole

    Specifications

    HS Code

    485262

    Chemical Formula C8H14N2
    Molecular Weight 138.21 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 248 - 250 °C
    Melting Point N/A
    Density 0.98 g/cm³ (at 20 °C)
    Solubility Soluble in organic solvents
    Flash Point 107 °C
    Vapor Pressure Low vapor pressure
    Ph Basic in nature

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    Frequently Asked Questions

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    What are the main uses of 1-butyl-2-methyl-imidazole?
    1 - butyl - 2 - methyl - imidazole, Chinese name 1 - butyl - 2 - methylimidazole, is an organic compound, which is widely used in the chemical and materials fields.
    First, it is often used as a key raw material in the preparation of ionic liquids. Ionic liquids have many excellent properties, such as low vapor pressure, high chemical stability and thermal stability. 1 - butyl - 2 - methylimidazole can be converted into ionic liquids with unique properties through specific reactions. In the field of organic synthesis, it can be used as a green solvent, which can effectively improve the reaction efficiency and separate the products conveniently. It can also reduce the environmental harm of traditional organic solvents.
    Second, in the field of materials science, 1-butyl-2-methylimidazole can participate in the preparation of functional materials. For example, introducing it into polymer materials can improve the solubility, thermal stability and ionic conductivity of materials. In the preparation of electrolyte materials for lithium-ion batteries, the use of materials containing this substance can optimize the conductivity and stability of batteries and improve the overall performance of batteries.
    Third, it also has outstanding performance in the field of catalysis. 1-butyl-2-methylimidazole can act as a ligand or catalyst to accelerate the process of specific chemical reactions. In some organic reactions, by virtue of its structural characteristics, it can complex with metal ions to form a high-efficiency catalyst, which realizes the regulation of reaction selectivity and activity, and then achieves better reaction effect.
    Fourth, in terms of gas adsorption and separation, the material prepared by 1-butyl-2-methylimidazole exhibits good adsorption performance for specific gases. For example, for acid gases such as carbon dioxide, it can achieve efficient adsorption and separation, which is of great significance in the field of environmental protection and resource recovery. It helps to reduce carbon dioxide emissions in industrial waste gas and achieve resource recycling.
    What are the physical properties of 1-butyl-2-methyl-imidazole?
    1 - butyl - 2 - methyl - imidazole is an organic compound with unique physical properties, as follows:
    It is a liquid at room temperature and pressure, and its appearance may be colorless to light yellow, clear and transparent. Due to the specific arrangement of carbon chains and imidazole rings in the molecular structure, the intermolecular force is moderate, and it cannot form a solid lattice, but it is enough to maintain a liquid condensed state.
    The substance has a measurable melting point and boiling point. The melting point is about -20 ° C, and the boiling point is roughly in the range of 250-270 ° C. The melting point is low, because the intermolecular force is not strong, and the molecule can be separated from the fixed position with a slight increase in energy; the boiling point is high, because there are forces such as van der Waals forces and hydrogen bonds (although weak) between molecules, more energy is required to make the molecule escape the liquid phase into the gas phase.
    The density of 1 - butyl - 2 - methyl - imidazole is nearly 0.96 - 0.98 g/cm ³, which is slightly smaller than that of water, so if mixed with water, it will float on the water. This density characteristic is also determined by the molecular structure and composition. The combination of hydrocarbon chains and imidazole rings makes the ratio of mass to volume have this value.
    Its solubility is manifested as being soluble in many organic solvents, such as ethanol, acetone, dichloromethane, etc. Because the compound is an organic molecule, it has similar chemical properties to organic solvents, and is mutually soluble according to the principle of "similar miscibility". It has limited solubility in water. Due to its non-highly polar molecules, it is difficult to form strong interactions with water molecules, and only a small amount can be dispersed in water.
    In addition, the compound has a certain viscosity, and the flow of molecules is hindered due to intermolecular interactions. Under specific conditions, it may also exhibit surface activity, changing surface properties at the interface, which is related to the distribution of hydrophilic and hydrophobic parts in the molecular structure.
    What is the chemistry of 1-butyl-2-methyl-imidazole?
    1 - butyl - 2 - methyl - imidazole is an organic compound. It has unique chemical properties. Under normal temperature, this substance may be in a liquid state. Looking at its properties, it has a certain fluidity, and its color may be nearly colorless and transparent, or slightly light.
    In terms of its solubility, it shows good affinity in organic solvents. Organic solvents such as alcohols and ethers can be mixed with it to form a uniform solution. However, in water, its solubility is relatively limited, only slightly soluble, due to the characteristics of the groups contained in the molecular structure.
    The chemical activity of 1-butyl-2-methyl-imidazole is considerable. Its molecular structure contains an imidazole ring, which has the characteristics of electron-rich, so it is easy to react with electrophilic reagents. Under suitable conditions, alkylation, acylation and other reactions can be carried out. Through these reactions, different functional groups can be introduced into the molecular structure, thereby expanding the types of derived compounds.
    In addition, this compound can act as a ligand or catalyst in some catalytic reactions. By virtue of its structural properties, it forms stable complexes with metal ions, thereby affecting the process and selectivity of the reaction. In the field of organic synthesis, it is often used to construct more complex organic molecular structures, contributing significantly to the development of organic synthetic chemistry.
    1-butyl-2-methyl-imidazole in what areas?
    1 - butyl - 2 - methyl - imidazole, an organic compound, is used in many fields.
    In the field of materials science, its use is quite wide. It can be used as an important component of ionic liquids. Ionic liquids have attracted much attention due to their unique physical and chemical properties, such as low vapor pressure, hot topic stability and excellent solubility. The ionic liquid composed of 1 - butyl - 2 - methyl - imidazole can be used as an efficient reaction medium in catalytic reactions, which can improve the reaction rate and selectivity. For example, in some organic synthesis reactions, it can promote fuller contact of the reactants, make the reaction conditions milder, and then improve the purity and yield of the product.
    It is also seen in the field of electrochemistry. The electrolyte made on this basis exhibits good ionic conductivity and can be used in high-performance battery systems. It can enhance the charging and discharging performance of the battery, prolong the service life of the battery, and improve the overall efficiency of the battery, which is of great significance in the development of modern energy storage devices.
    Furthermore, it also has potential applications in the field of biomedicine. Because it has certain affinity and solubility to certain biomolecules, it may be applied to drug delivery systems. With its characteristics, it can effectively wrap drug molecules, achieve controlled release of drugs, improve drug efficacy, and reduce the side effects of drugs on normal tissues.
    In the chemical separation process, 1-butyl-2-methyl-imidazole can also be used. Due to its different solubility to different substances, it can be used for separation operations such as liquid-liquid extraction to help efficiently separate and purify specific components in mixtures, and improve the quality and production efficiency of chemical production products.
    What are 1-butyl-2-methyl-imidazole synthesis methods?
    The synthesis of 1-butyl-2-methyl-imidazole, 1-butyl-2-methylimidazole, is as follows:
    One of the common methods for preparing 1-butyl-2-methylimidazole in the past is to start with 2-methylimidazole. First, 2-methylimidazole is combined with a halobutane, such as bromobutane, in a suitable solvent, adding a base as a catalyst, such as potassium carbonate, under the condition of heating and refluxing, nucleophilic substitution is performed. In the meantime, the butyl of halobutane is affected by alkali, and its nucleophilicity is enhanced. It attacks the nitrogen atom of 2-methylimidazole, and the halogen ions leave, so 1-butyl-2-methylimidazole is obtained. After distillation, recrystallization and other methods of refining, pure products can be obtained.
    There are also those who use imidazole as the starting material. Imidazole is methylated first, often with methylating reagents such as iodomethane, and 2-methylimidazole can be obtained in an alkaline environment, such as the presence of sodium hydride. Then, as the above method, 2-methylimidazole is reacted with halobutane, and 1-butyl-2-methylimidazole can also be obtained through the same refining steps.
    In addition, new technologies such as microwave radiation are also used. Under microwave radiation, 2-methylimidazole and halobutane are used as raw materials without traditional long-term heating and reflux, the reaction rate is greatly increased, and the yield can be improved. After the reaction, it still needs to be separated and purified to obtain high-purity 1-butyl-2-methylimidazole. This new technology saves time and energy, and is one of the best methods for synthesizing this compound.