4 Amino 3 Pyridinecarboxamide Hydrochloride
pyridine pyrrole pyrazine piperidine piperazine

4-amino-3-pyridinecarboxamide hydrochloride

    Specifications

    HS Code

    244937

    Chemical Formula C6H8ClN3O
    Molecular Weight 173.60
    Appearance Solid
    Solubility In Water Soluble
    Melting Point Typically in a certain range (data may vary)
    Pka Value Relevant to its acidic - basic properties (specific value may vary)
    Density Appropriate value if available
    Stability Stable under normal conditions if stored properly

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    General Information
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    Frequently Asked Questions

    As a leading 4-amino-3-pyridinecarboxamide hydrochloride 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 4-amino-3-pyridinecarboxamide hydrochloride?
    4-Amino-3-pyridinecarboxamide hydrochloride (4-amino-3-pyridinecarboxamide hydrochloride) is an organic compound. Its properties are common to salts, and it has good solubility in water due to the interaction between hydrochloride and organic cations.
    This substance is in the form of white to off-white crystalline powder, which is pure and uniform in texture. Its melting point is fixed, which can be an important basis for identification. It is still stable in chemical properties at room temperature, but when it encounters strong acids, strong bases or specific oxidants and reducing agents, it is easy to react chemically, and its structure or changes.
    In terms of acidity and alkalinity, because it contains amino groups, it has a certain alkalinity and can form salts with acids; and because of the state of hydrochloride, hydrogen ions can be dissociated in water, which is weakly acidic.
    Its spectral properties are also characterized. In infrared spectroscopy, amino groups, amide groups and other functional groups have unique absorption peaks, which can assist in structure identification. Nuclear magnetic resonance spectroscopy, hydrogen atom signals at different positions can provide key information for molecular structure analysis.
    The chemical properties of 4-amino-3-pyridinecarboxamide hydrochloride make it important for use in medicine, chemical industry and other fields. In pharmaceutical research and development, or involved in drug synthesis intermediates; in chemical industry, or for the preparation of special materials, all rely on its unique chemical properties.
    What are the main uses of 4-amino-3-pyridinecarboxamide hydrochloride?
    4-Amino-3-pyridinecarboxamide hydrochloride, which is 4-amino-3-pyridinecarboxamide hydrochloride, has a wide range of uses.
    In the field of pharmaceutical research and development, it is often the key intermediate for the synthesis of many drugs. The structure of geinopyridine and amides is very common in many bioactive molecules. With this as the starting material, various functional groups can be added by organic synthesis to create compounds with specific pharmacological activities. For example, in the development of drugs for the treatment of certain neurological diseases or cardiovascular diseases, the structure of the substance can lay the foundation for the construction of drug active ingredients, enabling researchers to design and synthesize new drugs with high affinity for disease-related targets.
    In the field of materials science, it also has unique uses. Because its molecular structure contains specific functional groups, it can participate in certain polymerization reactions or interact with other materials. It can be used as a functional monomer to polymerize with other monomers to form polymer materials with special properties, such as polymers with excellent optical, electrical or mechanical properties. These polymers may show unique application value in the fields of optoelectronic devices, sensors, etc., such as for the preparation of sensor materials that respond to specific substances, and achieve sensing functions through their specific interactions with target analytes.
    In chemical research, 4-amino-3-pyridineformamide hydrochloride is often used as a model compound, which helps researchers to further explore the mechanism of organic reactions. Because of its clear structure and certain reactivity, it can simulate the reaction behavior of more complex compounds. By studying the various reactions it participates in, such as nucleophilic substitution, electrophilic substitution, etc., researchers can deepen their understanding of the pathways and laws of organic reactions, providing theoretical basis and practical experience for the development of organic synthesis methodologies.
    What is the synthesis method of 4-amino-3-pyridinecarboxamide hydrochloride?
    The synthesis of 4-amino-3-pyridineformamide hydrochloride is an important topic in the field of organic synthesis. There are many methods, one of which is described in detail today.
    Starting materials, suitable pyridine derivatives can be selected. First, the specific position of the pyridine ring is substituted to introduce an amino group. This step requires careful selection of reaction conditions and reagents, such as nucleophilic substitution with specific amine reagents at appropriate temperature, pressure and catalyst. The catalyst used may be a metal salt, which helps the reaction to proceed efficiently.
    Next, another position of the pyridine ring is modified to introduce a formamide group. This process may involve an acylation reaction, in which the corresponding acylating reagent, under the catalysis of a suitable base, interacts with the pyridine derivative. The choice of base depends on the selectivity and rate of the reaction, and organic bases or inorganic bases are commonly used.
    After 4-amino-3-pyridineformamide is formed, to obtain hydrochloride, it can be dissolved in a suitable organic solvent, passed into hydrogen chloride gas or added concentrated hydrochloric acid. Hydrogen chloride and amino groups form salts, and pure 4-amino-3-pyridineformamide hydrochloride can be obtained through crystallization, filtration, drying, etc.
    Each step of the reaction requires close monitoring of the reaction process. TLC, NMR and other analytical methods are used to ensure that the reaction reaches the expected target and the product purity meets the requirements. The details of each step, such as precise control of reaction time, temperature, solvent selection and dosage, have a profound impact on the quality and yield of the final product.
    4-amino-3-pyridinecarboxamide hydrochloride in storage and transportation
    4-Amino-3-pyridineformamide hydrochloride, when storing and transporting, pay attention to many matters. This compound has specific chemical properties, and when stored, the first environment is dry. Because moisture can easily cause chemical reactions such as hydrolysis, which can damage the quality. Therefore, it should be placed in a dry, ventilated place without moisture intrusion. It can be packed in a sealed container to prevent moisture intrusion.
    Temperature is also critical. Avoid high temperatures, which may cause it to decompose or accelerate deterioration. Generally speaking, it can be stored at room temperature, but if there are special regulations, follow its instructions or refrigerate at low temperature.
    As for transportation, ensure that the packaging is stable. Due to the poor packaging of the substance, bumps and vibrations during transportation, or damage to the packaging, there is a risk of leakage. Leakage is not only a waste of materials, but also may endanger the environment and personal safety.
    And the transportation process should be kept away from fire sources, heat sources and strong oxidants. 4-Amino-3-pyridineformamide hydrochloride may react violently with strong oxidants, causing danger. Furthermore, transporters should be familiar with its chemical properties and emergency treatment methods. In case of an accident, they can respond properly in time to reduce losses and hazards. In this way, 4-Amino-3-pyridineformamide hydrochloride is safe during storage and transportation.
    What is the market price range for 4-amino-3-pyridinecarboxamide hydrochloride?
    The market price range of 4-amino-3-pyridineformamide hydrochloride often fluctuates due to various reasons. The key factor here is the purity of the product. Those with high purity are favored in fields with strict quality requirements such as scientific research and pharmaceuticals, and their price is naturally high; if the purity is slightly lower, it is mostly used for general industrial purposes, and the price is relatively low.
    Furthermore, the market supply and demand situation also affects its price. If there is a surge in demand for it at a certain time and the supply is difficult to keep up in time, the price will rise; conversely, if the market oversupply, the price will decline.
    The complexity of the production process is also a major factor. If the production process is cumbersome and requires many fine steps and high-end technology, the cost will inevitably increase, and the price will also rise.
    In addition, details such as sales channels and packaging specifications are also affected. Selling through specific professional channels, or using special packaging to ensure quality, the price may be different.
    According to past market conditions, low-purity (about 90%) products may cost between a few yuan and tens of yuan per gram; high-purity (98% and above), the price per gram may exceed 100 yuan, or even higher, reaching hundreds of yuan per gram, depending on the current market conditions.