2 Amino 1h Benzimidazole 5 Carboxylic Acid
quinoline thiophene imidazole thiazole

2-Amino-1H-benzimidazole-5-carboxylic acid

    Specifications

    HS Code

    175355

    Name 2-Amino-1H-benzimidazole-5-carboxylic acid
    Molecular Formula C8H7N3O2
    Molar Mass 177.16 g/mol
    Appearance Solid (usually white or off - white)
    Melting Point Decomposes rather than having a distinct melting point in normal conditions
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
    Pka Carboxylic acid pKa around 2 - 3 (approximate value for the acidic group)
    Basicity Weakly basic due to the amino group in the benzimidazole ring
    Stability Stable under normal conditions, but can react with strong acids, bases and oxidizing agents

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    General Information
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    Frequently Asked Questions

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    What are the main uses of 2-Amino-1H-benzimidazole-5-carboxylic acid?
    2-Amino-1H-benzimidazole-5-carboxylic acid, this substance has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new drugs. The genbenzimidazole structure is closely bound to specific targets in many drug molecules in the body, showing a variety of biological activities, such as anti-tumor, antibacterial, antiviral, etc. By structural modification and modification of 2-amino-1H-benzimidazole-5-carboxylic acid, innovative drugs with good efficacy and small side effects can be developed.
    In the field of materials science, it also has important uses. It can be used as a monomer for the synthesis of special functional materials, such as the preparation of polymer materials with excellent optical and electrical properties. Due to its unique molecular structure, it can endow materials with special properties, and is expected to be used in the manufacture of Light Emitting Diodes, solar cells and other devices in the field of optoelectronics.
    In chemical research, 2-amino-1H-benzimidazole-5-carboxylic acid is often used as an intermediate in organic synthesis. With its active groups, it can construct complex organic compounds through various chemical reactions, contributing to the development of organic synthesis chemistry, providing an effective way for the synthesis of novel organic molecules, and promoting the continuous progress of chemistry.
    What are the physical properties of 2-Amino-1H-benzimidazole-5-carboxylic acid?
    2-Amino-1H-benzimidazole-5-carboxylic acid, this material is special, with various characteristics such as color and taste. Under normal circumstances, it may be white to off-white powder. On a microscopic level, the powder is uniform and delicate, like frost and snow sprinkling. As for the smell, it is often light and almost non-existent. It is placed under the nose to smell lightly, and only feels a slight smell, but there is no pungent and unpleasant smell.
    Solubility is also the key to physical properties. In common organic solvents, its solubility in water is poor, just like raindrops falling on lotus leaves, and it is difficult to blend; however, in specific solvents such as dimethyl sulfoxide (DMSO), it can dissolve well, just like a fish getting water, gradually disappearing and integrating into the solvent.
    Melting point is also an important physical property characteristic. After rigorous determination, its melting point is in a specific temperature range. At this temperature, the material form gradually changes from solid to liquid, just like ice and snow melting, which is a critical moment for its molecular structure change.
    In terms of stability, under conventional environmental conditions, if the temperature is not too high, the humidity is not high, and there is no special chemical interference, its structure is relatively stable, and it can maintain its own characteristics for a long time. In the case of strong acid and alkali and other extreme chemical environments, it is like a delicate flower in a rainstorm, the structure is easily damaged, and the physical properties are also changed.
    Its acid-base characteristics cannot be ignored. Because it contains amino and carboxyl groups, it has both acid and base. In an acidic environment, amino groups can accept protons, just like sponges absorb water; in an alkaline environment, carboxyl groups can give protons, like people who open the purse generously. This property makes it play a unique role in different chemical systems.
    What is the chemical synthesis method of 2-Amino-1H-benzimidazole-5-carboxylic acid?
    To prepare 2-amino-1H-benzimidazole-5-carboxylic acid, the following method can be used.
    Take phthalamine and cyanoacetic acid as the starting material, and the two are mixed in an appropriate amount, usually with a molar ratio of about 1:1.2. Place it in an organic solvent such as ethanol or N, N-dimethylformamide, which can provide a homogeneous environment for the reaction and promote the reaction.
    Then, add an appropriate amount of catalyst, such as glacial acetic acid or p-toluenesulfonic acid. The function of the catalyst is to accelerate the reaction process and reduce the activation energy required for the reaction. The reaction system is heated to a suitable temperature, about 120-150 ° C. At this temperature, o-phenylenediamine and cyanoacetic acid will undergo a condensation reaction to form 2-aminobenzimidazole-5-nitrile. Continuous stirring is required at this stage to ensure that the reactants are uniformly heated and the reaction is fully promoted.
    After the reaction is completed, let the reaction solution cool. Then, pour the cooled reaction solution into an alkaline solution, such as sodium hydroxide or potassium hydroxide solution. This is a hydrolysis reaction step. The temperature is controlled at 60-80 ° C. 2-amino-benzimidazole-5-nitrile will be hydrolyzed to 2-amino-1H-benzimidazole-5-carboxylate under basic conditions.
    After hydrolysis is completed, carefully adjust the pH of the reaction solution to the acidic range with an acid, such as hydrochloric acid or sulfuric acid, about pH = 2-3. At this time, 2-amino-1H-benzimidazole-5-carboxylic acid will precipitate from the solution. Pure 2-amino-1H-benzimidazole-5-carboxylic acid products can be obtained through post-treatment processes such as suction filtration, washing, and drying. During the whole process, attention should be paid to the precise control of reaction conditions and the proper allocation of material proportions, so as to obtain the ideal yield and purity.
    Where is 2-Amino-1H-benzimidazole-5-carboxylic acid used?
    2-Amino-1H-benzimidazole-5-carboxylic acid is useful in many fields.
    In the field of medicine, this compound has attracted much attention. Due to its special structure, it has potential biological activity, or can be used as a key intermediate in drug development. For example, when developing anti-tumor drugs, it can participate in the construction of specific active structures, help the drug to accurately act on tumor cells, interfere with key processes such as tumor cell proliferation and differentiation, and is expected to contribute to the solution of tumor problems. Or in the development of antibacterial drugs, with its unique chemical properties, develop new antibacterial agents to deal with the increasingly serious problem of drug-resistant bacteria.
    In the field of materials science, it also has extraordinary performance. It can be treated by special processes to make it part of functional materials. For example, materials with special adsorption properties can be prepared for the adsorption and removal of heavy metal ions or organic pollutants in environmental water bodies to purify the water environment. It can also be integrated into polymer materials as additives to improve the mechanical properties and thermal stability of materials, and broaden the application range of polymer materials.
    In the field of agriculture, there are also possibilities. Or it can be reasonably modified and developed into a new type of plant growth regulator to regulate the process of plant growth and development, such as promoting seed germination, enhancing plant stress resistance, etc., to improve crop yield and quality, and provide assistance for agricultural harvest. From this perspective, 2-amino-1H-benzimidazole-5-carboxylic acid has shown broad application prospects in medicine, materials science, agriculture and other fields, and is a valuable compound.
    What is the market outlook for 2-Amino-1H-benzimidazole-5-carboxylic acid?
    2-Amino-1H-benzimidazole-5-carboxylic acid, this substance is promising in the field of pharmaceutical and chemical industry. Looking at the current market, it has attracted much attention in the creation of new drugs. Many scientific research talents have dedicated themselves to studying it, hoping to use it as a basis to develop effective drugs and treat intractable diseases.
    Because of its unique chemical structure, it has the potential to interact with many targets in organisms. Therefore, it may emerge in the development of anti-tumor, antiviral and other drugs. Looking at the past, many new compounds have shone in the field of medicine due to their specific structures, and this compound is also expected to follow in its footsteps.
    Furthermore, in the field of materials science, it may have different functions. For example, the preparation of polymer materials with special properties, with its chemical activity, or the optimization of material properties, broadens the boundaries of material applications. Although the relevant research has not been completed at present, it has seen the dawn. With time and advanced scientific research, it may be able to open up new opportunities in the field of materials, bringing unexpected changes to industrial production, daily life and many other aspects.
    Therefore, although 2-amino-1H-benzimidazole-5-carboxylic acid is still in the stage of development, the market prospect is just like the rising sun, with unlimited potential. When people of insight work together, it will surely bloom brightly.