4 Aminopyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

4-Aminopyridine-3-carboxylic acid

    Specifications

    HS Code

    158456

    Name 4-Aminopyridine-3-carboxylic acid
    Molecular Formula C6H6N2O2
    Molar Mass 138.12 g/mol
    Appearance Solid (usually white or off - white)
    Solubility In Water Moderate solubility
    Pka Value relevant for acidic and basic nature
    Boiling Point Decomposes before boiling
    Melting Point 253 - 255 °C
    Odor Odorless or very faint odor
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

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    What are the main uses of 4-aminopyridine-3-carboxylic acid?
    4-Hydroxypyridine-3-carboxylic acid is one of the organic compounds. It has a wide range of main uses and plays an important role in both the pharmaceutical and chemical fields.
    In the field of medicine, 4-Hydroxypyridine-3-carboxylic acid is often a key intermediate for the synthesis of drugs. Due to its unique chemical structure, it can participate in the construction of many drug molecules and endow drugs with specific biological activities and pharmacological functions. For example, some drugs with antibacterial and anti-inflammatory effects, 4-Hydroxypyridine-3-carboxylic acid is an indispensable raw material in the synthesis process. Through chemical modification and reaction, it can be integrated into the molecular structure of the drug, so that the drug can precisely act on specific targets in the body and exert the effect of treating diseases.
    In the chemical industry, this compound also shows important value. It can be used as a starting material for the synthesis of high-performance materials. With its chemical properties, it can react with other compounds to form polymers or materials with special properties. For example, in the preparation of some high-temperature and high-strength materials, 4-hydroxypyridine-3-carboxylic acids participate in the reaction, which helps to improve the stability and mechanical properties of the material. At the same time, in the dye industry, it can be used as an intermediate for the synthesis of specific color dyes, giving the dyes unique color and stability, and meeting the requirements of dye properties in different fields.
    In summary, 4-hydroxypyridine-3-carboxylic acids play a key role in the field of medicine and chemical industry due to their special chemical structure and reactivity, and are of great significance for promoting the development of related industries.
    What are the synthesis methods of 4-aminopyridine-3-carboxylic acid?
    There are various methods for the synthesis of 4-aminopyridine-3-carboxylic acids, which are described in detail as follows:
    First, pyridine is used as the initial raw material. 4-nitropyridine can be prepared by nitration reaction of pyridine under specific conditions. Next, 4-nitropyridine is reduced by catalytic hydrogenation or chemical reduction, for example, by converting nitro groups to amino groups to obtain 4-aminopyridine. Subsequently, 4-aminopyridine reacts with suitable carboxylating reagents, such as halocarboxylic acids or their derivatives, under the catalysis of bases, thereby introducing carboxyl groups, and finally synthesizing 4-aminopyridine-3-carboxylic acids. This path step is relatively clear, but the regioselectivity of the nitrification reaction needs to be properly controlled to prevent excessive by-products.
    Second, start from nitrogen-containing heterocyclic compounds. Select nitrogen-containing heterocyclic rings with suitable structures, and gradually build target molecules through a series of functional group conversion reactions. For example, some specific fused ring nitrogen-containing compounds, through ring opening, functional group modification and other reactions, first form a pyridine ring skeleton, and then introduce amino and carboxyl groups in a targeted manner. This approach requires quite high selection of starting materials, and it may be difficult to obtain raw materials. However, if the raw materials are selected properly, some reaction steps may be simplified.
    Third, the coupling reaction is catalyzed by transition metals. For example, halogenated pyridine derivatives are coupled with amino and carboxyl-containing related reagents under the catalysis of transition metal catalysts such as palladium and copper. First, the halogen check point on halogenated pyridine is coupled with the amino-containing reagent to introduce the amino group, and then the carboxyl group is introduced through another coupling reaction or carboxylation reaction. Such methods have relatively mild reaction conditions and good selectivity, but the cost of transition metal catalysts is high, and the separation and recovery of the catalyst after the reaction may be problematic.
    Fourth, biosynthesis. Using the catalytic properties of microorganisms or enzymes, 4-aminopyridine-3-carboxylic acids are synthesized through complex metabolic pathways in organisms using specific substrates as raw materials. This method has the advantages of green and environmental protection, with high selectivity. However, the biological system is complex, the control requirements for reaction conditions are strict, and it is difficult to increase the yield. Large-scale production requires in-depth research and optimization.
    What are the physical and chemical properties of 4-aminopyridine-3-carboxylic acids?
    4-Hydroxypyridine-3-carboxylic acid, this is an organic compound. Its physical and chemical properties are quite characteristic and widely used in many fields.
    Looking at its physical properties, under normal temperature and pressure, 4-hydroxypyridine-3-carboxylic acid is often in a solid state. This substance has a certain solubility in water, but the solubility is also affected by factors such as temperature. Generally speaking, when the temperature increases, its solubility in water will also increase accordingly.
    In terms of chemical properties, 4-hydroxypyridine-3-carboxylic acids are acidic due to the presence of carboxyl groups. The carboxyl group can ionize hydrogen ions under suitable conditions, and then exhibit acidity. It can neutralize with bases to form corresponding salts and water. At the same time, the hydroxyl group also imparts specific reactivity to the compound. Hydroxyl groups can participate in esterification reactions, and when combined with suitable acids under the action of catalysts, ester compounds can be formed.
    In addition, the pyridine ring structure of 4-hydroxypyridine-3-carboxylic acids gives it a certain aromaticity, and the electron cloud distribution characteristics on the pyridine ring enable it to undergo reactions such as electrophilic substitution. However, due to the influence of the substituents on the ring, the reactivity and selectivity will also vary. In the field of organic synthesis, 4-hydroxypyridine-3-carboxylic acid is often used as a key intermediate. Through a series of chemical reactions, a variety of organic compounds with biological activity or special functions can be prepared, which are of great value in medicinal chemistry, materials science, etc.
    What is the price of 4-aminopyridine-3-carboxylic acid in the market?
    The price of various things in the market often varies according to time, place, and supply and demand. As for the price of 4-hydroxypyridine-3-carboxylic acid, this rule is also followed.
    The price of this chemical product is related to multiple ends. First, it is difficult and easy to make. If the preparation method is complicated, and many raw materials, exquisite techniques and harsh conditions are required, the cost will be high, and the price will follow. Suppose its synthesis requires rare materials, or through multiple reactions, each step has losses, or special equipment and conditions, so it is expensive, and it must be sold at a high price in the market.
    Second, the situation of supply and demand is also. If there are many people who need this product in the pharmaceutical, chemical and other industries, and the demand exceeds the supply, the price will rise. For example, when a new drug is developed, it needs to be used as a key raw material, and pharmaceutical companies compete to buy it, and its price will rise. On the contrary, if the supply exceeds the demand, there will be more producers, but there will be less users. In order to sell its goods, the price will be reduced.
    Furthermore, the competition in the market will also have an impact. If there are many of these, they will compete with each other for profits, and the price will be reduced in order to win customers, and the price will tend to be lower. If there are few producers, it will almost become a monopoly, and the price can be set higher.
    Also, the distance of the land and the difficulty of transportation are also related to the price. If the origin is far away, plus freight and preservation fees If transportation requires special methods, such as refrigeration, sealing, etc., the cost will also increase, and the price will be expensive.
    Although it is difficult to determine the current market price of 4-hydroxypyridine-3-carboxylic acid, according to the above factors, if it is easy to prepare, more supply and less demand, intense competition and easy to transport, the price will be low; on the contrary, if it is difficult to control, more supply and less supply, monopoly and difficult to transport, the price will be high. Buyers who enter the market should carefully observe the market conditions and review the situation when they need to, in order to obtain a suitable price.
    What are the application fields of 4-aminopyridine-3-carboxylic acid
    4-Hydroxypyridine-3-carboxylic acid, an important organic compound, is widely used in many fields.
    In the field of medicine, it shows significant value. In the synthesis of many drugs, 4-hydroxypyridine-3-carboxylic acid is often used as the key intermediate. Due to its unique chemical structure, it can participate in a variety of chemical reactions, and then construct compounds with specific pharmacological activities. For example, some drugs used to treat cardiovascular diseases, during the synthesis process, 4-hydroxypyridine-3-carboxylic acid can be introduced through a series of reactions to introduce specific functional groups, giving the drug a precise target and therapeutic effect. For example, in the development of anti-tumor drugs, it may also be used as a key structural unit to help build molecules with high anti-tumor activity.
    In the field of materials science, it also has outstanding performance. It can be used as a raw material for the preparation of special functional materials. With its structural properties, it can regulate the properties of materials during polymerization reactions and other processes. For example, when preparing polymer materials with specific optical and electrical properties, 4-hydroxypyridine-3-carboxylic acids can be used as functional monomers to participate in polymerization, so that the resulting materials have unique photoelectric conversion properties, electrical conductivity, etc., and have potential applications in optoelectronic devices, sensors, etc.
    Furthermore, in the field of pesticides, its role cannot be underestimated. Can be used to synthesize new pesticides. Pesticide compounds with high insecticidal, bactericidal or herbicidal activities are designed and synthesized by using their special affinity for certain biological activity check points. Such pesticides based on 4-hydroxypyridine-3-carboxylic acids are expected to have higher selectivity and environmental friendliness, reduce the impact on non-target organisms, and improve the control effect.
    In addition, in organic synthetic chemistry research, 4-hydroxypyridine-3-carboxylic acids are an important synthetic building block, providing chemists with rich reaction possibilities. Through functional group transformation and modification, complex and diverse organic compounds can be constructed, which can promote the development of organic synthetic chemistry and lay the foundation for innovative applications in more fields.