5 Methyl 4 Hydroxymethyl Imidazole Hcl
quinoline thiophene imidazole thiazole

5-METHYL-4-HYDROXYMETHYL IMIDAZOLE HCL

    Specifications

    HS Code

    671693

    Chemical Name 5-METHYL-4-HYDROXYMETHYL IMIDAZOLE HCL
    Molecular Formula C5H7N2OCl
    Molecular Weight 146.575 g/mol
    Appearance Typically a solid powder
    Solubility Soluble in certain polar solvents
    Melting Point Specific value would depend on purity and measurement method
    Ph Affects the solution pH when dissolved
    Stability Stable under normal storage conditions
    Odor May have a characteristic odor

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    5-METHYL-4-HYDROXYMETHYL chemical structure of IMIDAZOLE HCL
    5 - METHYL - 4 - HYDROXYMETHYL IMIDAZOLE HCL is an organic compound. In its chemical structure, the imidazole ring is the core structure. The imidazole ring has the shape of a five-membered nitrogen-containing heterocycle, which is composed of two nitrogen atoms and three carbon atoms. The special distribution of electron clouds in the ring makes the ring have certain aromaticity, which is the basis for many chemical properties of the compound.
    At the 4th position of the imidazole ring, there is a hydroxymethyl (-CH 2O OH) group attached. In this hydroxymethyl group, the carbon atom is connected to the imidazole ring by a single bond, and the hydroxyl group (-OH) is connected to the carbon atom. The presence of hydroxyl groups imparts certain hydrophilicity to the compound, and due to the high electronegativity of oxygen atoms, hydroxyl groups can participate in the formation of hydrogen bonds, which has a great impact on the physical and chemical properties of the compound.
    And at the 5th position of the imidazole ring, there is a methyl (-CH
    ) group connected. Methyl is the power supply group, and its presence affects the electron cloud density of the imidazole ring, altering the electron cloud distribution of each atom on the ring, thereby affecting the reactivity and selectivity of the compound.
    In addition, the compound binds to hydrochloric acid (HCl). In the formed salt, the hydrogen ion of hydrochloric acid binds to the nitrogen atom on the imidazole ring to form a positively charged ion, while the chloride ion balances the charge with it. The formation of this salt greatly changes the physical properties of the compound, such as solubility, which is usually better in water, and its application in organic synthesis, medicinal chemistry and other fields is also different. Therefore, the chemical structure of 5-METHYL-4-HYDROXYMETHYL IMIDAZOLE HCL is composed of an imidazole ring and an ion pair formed by hydroxymethyl, methyl and hydrochloric acid connected at a specific position on the ring. The interaction of each part determines the unique properties and uses of the compound.
    5-METHYL-4-HYDROXYMETHYL the main uses of IMIDAZOLE HCL
    5-Methyl-4-hydroxymethylimidazole hydrochloride is an important chemical substance that has significant uses in many fields.
    First, in the field of medicine, it is often used as a key intermediate in drug synthesis. Due to the specific chemical structure of this compound, it can be converted into a drug molecule with specific pharmacological activity through a series of reactions. For example, it can participate in the synthesis of certain antibacterial drugs. Through its structural properties, it can enhance the effect of drugs on pathogens and help fight infectious diseases.
    Second, in the field of materials science, 5-methyl-4-hydroxymethylimidazole hydrochloride also plays an important role. It can be used to prepare functional polymer materials because it can polymerize with other monomers, giving the material unique properties. Such as improving the thermal stability and mechanical properties of the material, so that the material can still maintain good physical properties under high temperature or stressed environment, and is widely used in aerospace, automobile manufacturing and other industries that require strict material properties.
    Furthermore, in the field of organic synthesis chemistry, it is a commonly used reagent. In many organic reactions, it can act as a catalyst or reaction substrate to promote the synthesis of complex organic compounds. With its unique chemical activity, it guides the reaction in the desired direction, improves the selectivity and yield of the reaction, and provides a powerful tool for organic synthesis chemists to help synthesize various novel and special functional organic compounds.
    5-METHYL-4-HYDROXYMETHYL the physical properties of IMIDAZOLE HCL
    5-Methyl-4-hydroxymethylimidazole hydrochloride, the physical properties of this substance are quite important. Its properties are often white to off-white crystalline powder, with fine and uniform texture. In terms of solubility, it is easily soluble in water, and can be quickly dispersed and dissolved in water to form a uniform solution. This characteristic makes it advantageous in the application of many aqueous systems. Its melting point has a certain range, about a specific value. This melting point characteristic is of great significance for identification and processing under specific temperature conditions. Furthermore, in terms of stability, it can maintain a relatively stable state under conventional environmental conditions. When encountering extreme temperatures, humidity or specific chemicals, corresponding chemical changes may occur. In addition, its density is also a specific value, which provides key parameters for precise control in operations such as material measurement and mixing. Overall, these physical properties play a crucial role in its application in many fields such as chemical industry and medicine, helping practitioners to use it rationally according to its characteristics and maximize its effectiveness.
    5-METHYL-4-HYDROXYMETHYL the production method of IMIDAZOLE HCL
    The production method of 5-methyl-4-hydroxymethymethylimidazole hydrochloride is an important technique in chemical technology. The method is usually obtained from a specific raw material through multi-step reaction.
    Initially, a compound containing a suitable substituent is selected as the starting material. If an organic molecule with an appropriate functional group is used under suitable reaction conditions, the basic structure of the imidazole ring is first constructed. This process often requires precise control of reaction temperature, pH and the proportion of reactants.
    Subsequently, the imidazole ring is modified at a specific position. To obtain the structure of 5-methyl-4-hydroxymethyl, it is necessary to introduce the methyl group at a specific reaction check point by suitable methylation reagents. In this step, the activity of the reagent and the choice of the reaction solvent are crucial, which are related to the selectivity and yield of methylation.
    Furthermore, the operation of introducing hydroxymethyl groups. Reagents that can provide hydroxymethyl groups are often used to connect the hydroxymethyl group to the 4 position of the imidazole ring under a catalyst or a specific reaction environment. This step also requires careful regulation of the reaction conditions to ensure that the reaction proceeds in the expected direction and avoid side reactions.
    After the structure of the imidazole ring and the construction of the substituent are completed, the last step is to form 5-methyl-4-hydroxymethylimidazole hydrochloride by interacting with hydrochloric acid. This salt formation reaction requires attention to the concentration, amount and reaction time of hydrochloric acid to obtain a high-purity target product.
    The entire production process requires fine control at every step, from the purity of the raw materials, the optimization of the reaction conditions, to the separation and purification of the product, all of which have a profound impact on the quality and yield of the final product.
    5-METHYL-4-HYDROXYMETHYL the precautions when using IMIDAZOLE HCL
    5-Methyl-4-hydroxymethylimidazole hydrochloride, this is a chemical substance. When using, many things need to be paid attention to.
    First safety protection. Because it may be corrosive and irritating, be sure to wear appropriate protective equipment when contacting. For example, wear protective gloves to prevent it from touching the skin, causing skin damage, redness, swelling, pain, etc.; wear protective glasses to avoid splashing into the eyes, causing serious injuries to the eyes, such as burns.
    Times and operating environment. It needs to be operated in a well-ventilated place. If the ventilation is poor, its volatile gaseous substances will accumulate, or cause respiratory discomfort, and even poisoning. The operating table should also be kept clean and dry to prevent impurities from mixing in and affecting its chemical properties and use effect.
    Furthermore, the number of access should be precisely controlled. According to the amount required for experiment or production, measure accurately to avoid waste. Excessive use not only consumes resources, improper subsequent treatment, but also causes environmental problems. After use, the container must be sealed in time to prevent it from absorbing moisture, oxidizing or reacting with other components in the air and causing it to deteriorate.
    Repeat, storage is also exquisite. It should be stored in a cool, dry and dark place, away from fire sources and oxidants. High temperature, humidity and light may affect its stability and accelerate deterioration. Contact with oxidants, or cause violent chemical reactions, endangering safety.
    Finally, after use, properly dispose of the remaining substances and waste. Do not dump at will, should follow the relevant environmental regulations, harmless treatment, so as not to pollute the environment.