5 Aminoimidazole 4 Carboxamide Hcl
quinoline thiophene imidazole thiazole

5-aminoimidazole-4-carboxamide HCl

    Specifications

    HS Code

    202239

    Name 5 - aminoimidazole - 4 - carboxamide HCl
    Chemical Formula C4H6N4O·HCl
    Molecular Weight 162.58 g/mol
    Appearance White to off - white solid
    Solubility In Water Soluble
    Melting Point 290 - 295 °C (decomposes)
    Pka 2.98 (for the conjugate acid of the amino group)
    Odor Odorless
    Stability Stable under normal conditions, but sensitive to heat and humidity

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    General Information
    Where to Buy 5-aminoimidazole-4-carboxamide HCl in China?
    As a trusted 5-aminoimidazole-4-carboxamide HCl manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 5-aminoimidazole-4-carboxamide HCl 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 5-aminoimidazole-4-carboxamide HCl?
    5 - aminoimidazole - 4 - carboxamide + HCl is a kind of organic compound. This compound has unique chemical properties. Its physical properties, at room temperature or as a solid, but the specific color, crystal form, etc., vary according to the preparation and purification.
    In terms of chemical activity, the amino group of 5 - aminoimidazole - 4 - carboxamide is alkaline and can react with acids to form salts, which is the reason for binding to HCl. The resulting salt is more soluble in water or better than its free base form. Due to ionization, it is more easily dispersed in polar solvents. < Br >
    Its chemical stability can be maintained under suitable conditions. When it encounters strong acids, strong bases, high temperatures or specific catalysts, it may react chemically. If in a strongly alkaline environment, some chemical bonds in its structure may be destroyed, causing molecular rearrangement or decomposition.
    And because its structure contains nitrogen heterocycles and amino groups, it can participate in a variety of organic synthesis reactions. In the field of medicinal chemistry, or as a key intermediate, it is used to create biologically active compounds. Because the structure of nitrogen heterocycles is often related to biological activities and can be specifically bound to targets in organisms, amino groups can also be chemically modified to modify the physicochemical properties and biological activities of compounds. < Br >
    In terms of storage, it needs to be placed in a dry and cool place to avoid contact with oxidants, acids and bases and other substances to prevent deterioration. Its diverse chemical properties make it important for potential applications in many fields such as organic synthesis and drug development.
    What are the main uses of 5-aminoimidazole-4-carboxamide HCl?
    5-Aminoimidazole-4-carboxamide hydrochloride (5-aminoimidazole-4-carboxamide + HCl) has a wide range of uses. In the field of medicine, it is often used as an intermediate for drug synthesis. In the development of many innovative drugs for the treatment of cancer, diabetes and other diseases, it is necessary to use this as the starting material through a series of chemical reactions to carefully construct complex molecular structures with specific pharmacological activities. It can participate in the biosynthetic pathway of purine nucleotides and affect cell metabolism and proliferation, so it is of great significance in the development of anti-cancer drugs.
    In the field of biochemical research, 5-aminoimidazole-4-formamide hydrochloride can be used as a tool to explore intracellular signaling pathways and metabolic regulation mechanisms. Scientists use its intervention in cell metabolism to gain insight into how cells respond to external stimuli and regulate their own metabolic activities, providing key clues for explaining the basic principles of life activities.
    In the field of agriculture, it may be used to develop new plant growth regulators. Because it can affect the metabolism and division of plant cells, or help optimize crop growth and development, improve crop yield and quality, and enhance plant tolerance to environmental stress, such as drought, salinity and other adverse conditions.
    What is the synthesis method of 5-aminoimidazole-4-carboxamide HCl?
    The synthesis of 5-aminoimidazole-4-carboxamide hydrochloride (5-aminoimidazole-4-carboxamide + HCl) is an important topic in the field of organic synthesis. Its synthesis method often follows the path of multi-step reaction.
    In the initial step, suitable starting materials are often used to construct the basic structure of the imidazole ring through condensation reaction. For example, select suitable compounds containing nitrogen and carbon, and make them interact under specific reaction conditions. The reaction conditions are very critical, such as temperature, pH, reaction solvent, etc., all need to be carefully regulated. If the temperature is too high or too low, the reaction can be biased in an unfavorable direction, or side reactions can be increased, or the reaction rate is too slow.
    After the imidazole ring is constructed, an amino group and a carboxyamide group need to be introduced. When introducing an amino group, a specific amination reagent can be used to promote the amino group to replace the atom or group at a specific position in the presence of a suitable catalyst. In this process, the choice of catalyst is crucial, and its activity and selectivity directly affect the efficiency of the reaction and the purity of the product.
    The introduction of carboxyamide groups also needs to be precisely controlled. Or through an acylation reaction, a suitable acylating reagent can be used to interact with the imidazole ring derivative to achieve the connection of carboxyamide groups. During the reaction process, the reaction process should be closely monitored, and the reaction degree can be known in real time by means of thin layer chromatography (TLC), so that the reaction can be stopped in time and the target product can be obtained.
    Finally, the product can be purified through a series of post-processing operations, such as extraction, washing, recrystallization, etc., to obtain high-purity 5-aminimidazole-4-formamide hydrochloride. Each step requires careful operation by the experimenter, insight into the reaction mechanism, and grasp the details of the reaction in order to successfully complete the synthesis.
    What are the precautions for 5-aminoimidazole-4-carboxamide HCl in storage and transportation?
    5-Aminoimidazole-4-carboxamide hydrochloride (5-aminoimidazole-4-carboxamide + HCl) is also a chemical substance. When storing and transporting, many matters need to be paid attention to.
    First words storage. This substance should be stored in a cool, dry and well-ventilated place. If the environment is humid, moisture can easily interact with it, or cause its properties to change, such as deliquescence, which in turn affects its quality and utility. And if the temperature is too high, it may also trigger chemical reactions, causing it to decompose or deteriorate. Therefore, it is necessary to avoid light and cool, and maintain a dry environment to ensure its stability.
    On transportation. When transporting, it is necessary to ensure that the packaging is intact. Because the substance may have certain chemical activity, if the packaging is damaged, contact with external substances, or accidental chemical reactions occur. And the transportation process should avoid violent vibration and collision to avoid damage to the packaging by impact. At the same time, the transporter needs to know its chemical properties, and in case of leakage, it can be properly disposed of in time to ensure the safety of personnel and the environment.
    In short, in the storage and transportation of 5-aminoimidazole-4-formamide hydrochloride, pay attention to environmental conditions and packaging conditions, which is the key to maintaining its stability and ensuring transportation safety.
    What is the market price range for 5-aminoimidazole-4-carboxamide HCl?
    The price of 5-aminoimidazole-4-carboxamide + HCl in the market varies depending on quality, source and quantity. If you buy from ordinary pharmacies and take a small amount, the price per gram may range from tens to hundreds of yuan. However, this is a rough estimate, and the market conditions are changeable and cannot be held together.
    If you buy from chemical raw material suppliers and buy in bulk, if the quantity is in kilograms, the price per kilogram may be reduced to about 1,000 yuan. Due to bulk purchase, the cost is slightly reduced, and merchants also make profits for sales. < Br >
    Also, those with excellent quality and high purity will have a high price. If used in precision fields such as pharmaceutical research and development, the purity requirements are strict, and the price is several times higher than that of ordinary ones.
    To know the exact price, when consulting different suppliers, the quality, quantity and price of their goods can be obtained. And the market conditions change with changes in supply and demand, and the cost of raw materials rises and falls. Regular surveys can obtain real-time prices.