4 Nitro 2 Pyridinecarboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

4-Nitro-2-pyridinecarboxylic acid

    Specifications

    HS Code

    532993

    Name 4-Nitro-2-pyridinecarboxylic acid
    Molecular Formula C6H4N2O4
    Molecular Weight 168.107 g/mol
    Appearance Yellow solid
    Melting Point 217 - 221 °C
    Solubility In Water Slightly soluble
    Pka 2.96
    Density 1.574 g/cm³
    Flash Point 193.3 °C
    Refractive Index 1.617

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    General Information
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    Frequently Asked Questions

    As a leading 4-Nitro-2-pyridinecarboxylic acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemistry of 4-Nitro-2-pyridinecarboxylic acid?
    4-Nitro-2-pyridinecarboxylic acid, this is an organic compound. In its molecular structure, the second position of the pyridine ring is connected with a carboxyl group, and the fourth position is a nitro group. Its chemical properties are particularly important and have applications in many fields.
    Let's talk about its acidity first. Due to its carboxyl group, this compound is acidic. The carboxyl group can dissociate hydrogen ions and establish dissociation equilibrium in water. Its acidity is closely related to the chemical environment in which the carboxyl group is located. The electronic effect of the pyridine ring has a great influence. The nitro group is a strong electron-absorbing group. Through the induction effect and conjugation effect, the electron cloud density of the carboxyl group decreases, making hydrogen ions more easily dissociated, so the acidity is stronger than that of benzoic acid.
    Let's talk about its redox Nitro is an oxidizing group that can be reduced under certain conditions. In case of suitable reducing agents, nitro can be gradually converted into amino groups and go through intermediate states such as nitroso and hydroxylamine. The pyridine ring itself also has certain redox activity. Under the action of strong oxidants, the pyridine ring may be destroyed or oxidized.
    In addition, 4-nitro-2-pyridine carboxylic acid can participate in nucleophilic substitution reactions. Due to the electron-absorbing action of nitro groups, the electron cloud density on the pyridine ring decreases, especially the nitro o-ortho-para-position, which is more susceptible to attack by nucleophilic reagents. Nucleophiles can replace the hydrogen atom on the pyridine ring to form various derivatives, which is of great significance in organic synthesis, and can be used to construct organic compounds with different structures.
    Under high temperature or in a specific chemical environment, this compound may undergo decomposition reactions. The decomposition products depend on the specific reaction conditions, or form nitrogen-containing gases, carbon dioxide and other small molecule compounds.
    In summary, 4-nitro-2-pyridinecarboxylic acid plays a key role in the fields of organic synthesis, medicinal chemistry and other fields due to its unique structure. In-depth exploration of its chemical properties can provide strong support for the development of related fields.
    What are the common synthesis methods of 4-Nitro-2-pyridinecarboxylic acid?
    There are many ways to synthesize 4-nitro-2-pyridinecarboxylic acid. The ancient method was obtained by nitrification and carboxylation of pyridine as a group. At first, pyridine was nitrified with an appropriate nitrifying agent, such as mixed acid (mixture of nitric acid and sulfuric acid), at a suitable temperature and time, and nitropyridine was obtained. Later, nitropyridine was carboxylated, and carbon dioxide was often used to react with metal reagents, or in the environment of strong bases and high temperatures, carboxyl groups were introduced to form 4-nitro-2-pyridinecarboxylic acid.
    Pyridine derivatives were used as the beginning. For example, 2-methylpyridine is first nitrified with nitric acid to obtain nitro-2-methylpyridine, and then oxidized to convert the methyl group into a carboxyl group. The oxidizing agent can be selected as a strong oxidizing agent such as potassium permanganate and potassium dichromate. In the system of water or organic solvent, it can be carried out at a suitable temperature to obtain the target compound.
    There is also a method of catalysis by transition metals. Using halide or borate containing pyridine structure as raw material, carbon monoxide and suitable nucleophiles, under the catalysis of transition metals (such as palladium, nickel, etc.), carbonylation occurs, and 4-nitro-2-pyridine carboxylic acid can be precisely synthesized. This approach has mild conditions and good selectivity, making it a common method for synthesis today.
    All kinds of synthesis methods have their own advantages and disadvantages. Although the ancient method has simple steps, the conditions are harsh, and the yield may not be good. With pyridine derivatives as the starting point, the step of oxidation or by-production affects the purity. Although the method of transition metal catalysis has advantages, the metal catalyst is expensive, and the post-treatment needs to be considered. Each method needs to be refined to meet different needs.
    Where is 4-Nitro-2-pyridinecarboxylic acid used?
    4-Nitro-2-pyridinecarboxylic acid, which is used in various fields such as chemical industry and medicine.
    In the chemical industry, it is often used as an intermediary in organic synthesis. With exquisite chemical techniques, it can be used to construct multiple and complex organic compound structures. For example, in the process of dye synthesis, it can participate in a series of reactions with unique chemical properties, giving dyes a bright color and excellent stability, making dyes shine in fabric printing and dyeing and other industries, making fabrics colorful and durable.
    In the field of medicine, its application is also very critical. Because of its special molecular structure, it has potential biological activity. Researchers can use it as a key starting material to develop therapeutic drugs for specific diseases through fine chemical modification and pharmacological research. Like in the field of anti-tumor drug development, it may participate in the construction of targeted drug molecules that precisely act on tumor cells, inhibit their growth and spread, and provide new opportunities and hope for overcoming cancer diseases. It helps medical science to continuously reach new heights and save the lives of many patients.
    What is the market price of 4-Nitro-2-pyridinecarboxylic acid?
    4-Nitro-2-pyridinecarboxylic acid, in the chemical market, its price varies from time to time, and also varies with quality and quantity. In the past, its market conditions were influenced by multiple factors.
    If looking at past transactions, its price is often determined by the price of raw materials. The price of 4-nitro-2-pyridinecarboxylic acid is also stable and low; if the raw material is rare, its price will increase. For example, if the supply of pyridine and nitro raw materials used in synthesis is sufficient and the price does not change significantly, then 4-nitro-2-pyridinecarboxylic acid is on the market, and the price may be maintained within a certain range, and both buyers and sellers negotiate according to this.
    Furthermore, the trend of supply and demand is also the key. If there are many people in the market who want it, but there are few people who produce it, the so-called "rare things are expensive", its price will rise. If the pharmaceutical industry has a large increase in demand for it at a certain time, and the manufacturer fails to expand production in time, its price will go up all the way. On the contrary, if the supply exceeds the demand, the manufacturer will sell it, or will reduce the price to sell it.
    Whether the process is advanced or not also depends on its price. If there is a new technology that can reduce consumption and improve production and reduce its cost, the price may be lower. In the past, some manufacturers improved the synthesis process to increase output and reduce impurities, and its market price was lower than that of the same industry, in order to compete for market share.
    In summary, the market price of 4-nitro-2-pyridinecarboxylic acid is variable, and it often changes due to raw materials, supply and demand, and processes. To know the real-time price, you need to look at the current market situation and consult industry experts to obtain a more accurate number.
    What are the storage conditions for 4-Nitro-2-pyridinecarboxylic acid?
    4 - Nitro - 2 - pyridinecarboxylic acid is a nitropyridinecarboxylic acid compound, and its storage conditions are very critical. This compound should be placed in a cool, dry and well-ventilated place. In a cool environment, it can avoid the change of its properties caused by high temperature, and the material will deteriorate due to high temperature or molecular structure changes. The dry place is to prevent it from being damp, and the moisture or chemical reaction with the acid will affect the purity and quality. Well-ventilated can disperse harmful gases that may evaporate in time to ensure the safety of the storage environment.
    In addition, keep away from fires and heat sources. Both open flames and high-temperature heat sources may cause the compound to burn or even explode, because it may have certain flammability and instability. At the same time, it should be stored separately from oxidizing agents and reducing agents. Oxidizing agents may react violently with 4-Nitro-2-pyridinecarboxylic acid, releasing a large amount of energy and causing danger; reducing agents may also react with it in complex chemical reactions, damaging its chemical properties.
    When storing, the package must be sealed. The sealed package can block external air, moisture and impurities, maintain the purity of the substance, and ensure the stability of the properties during the storage period. After taking it, it should be sealed in time to prevent the remaining part from being affected by environmental factors. In short, following these storage conditions can effectively ensure the quality and safety of 4-Nitro-2-pyridinecarboxylic acid.