2 Amino 4 Methyl 5 Nitropyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Amino-4-methyl-5-nitropyridine

    Specifications

    HS Code

    900276

    Chemical Formula C6H7N3O2
    Appearance Solid (usually yellowish - colored solid)
    Odor May have a characteristic odor, often described as pungent
    Melting Point Typically in the range of 180 - 185°C
    Boiling Point Decomposes before boiling under normal conditions
    Solubility In Water Slightly soluble in water
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF
    Pka pKa values can vary, but for the amino group it may be around 4 - 5
    Stability Stable under normal conditions, but sensitive to strong acids, bases and reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-Amino-4-methyl-5-nitropyridine 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 main uses of 2-amino-4-methyl-5-nitropyridine?
    2-Amino-4-methyl-5-pyrimidinecarboxylic acid, which is an important organic synthesis intermediate, is widely used in many fields such as medicine and pesticides.
    In the field of medicine, it is a key raw material for the synthesis of various drugs. For example, in the development of antimalarial drugs, through specific chemical reactions, a molecular structure with antimalarial activity is constructed on this basis, which can interfere with the metabolic process of Plasmodium or destroy its cell structure to achieve the purpose of treating malaria. In the field of anti-tumor drug research and development, compounds that can target specific targets of tumor cells can be synthesized by chemically modifying them, blocking the proliferation of tumor cells and inducing their apoptosis, thus providing effective drug options for combating tumor diseases.
    In the field of pesticides, 2-amino-4-methyl-5-pyrimidinecarboxylic acid can be used to create new pesticides. For example, the synthesis of pesticides with high insecticidal activity, its unique chemical structure can specifically act on the nervous system or physiological and metabolic links of pests, accurately kill pests, and have little impact on the environment and non-target organisms, which is in line with the current green and environmental protection pesticide development concept. It can also be used to synthesize pesticides with bactericidal function. By inhibiting the growth and reproduction of pathogenic bacteria, it protects crops from diseases and ensures crop yield and quality.
    In addition, in the field of fine chemicals, it is an important organic synthesis block and participates in the synthesis of various functional materials, dyes, etc. With its special chemical properties and structure, it endows materials or dyes with unique properties, such as improving material stability, enhancing dye color and fastness, etc.
    To sum up, 2-amino-4-methyl-5-pyrimidinecarboxylic acid plays a key role in many fields due to its indispensable position, which is of great significance to promoting the development of related industries.
    What are the physical properties of 2-amino-4-methyl-5-nitropyridine?
    2-% hydroxy-4-methyl-5-pyrimidinone is an organic compound with unique physical properties. Its properties are usually white to light yellow crystalline powder, which is stable at room temperature and pressure, which is the basis for its existence and application in many environments.
    Looking at its solubility, 2-% hydroxy-4-methyl-5-pyrimidinone can be soluble in some organic solvents, such as methanol, ethanol, etc. This property makes it possible to use it as a reactant or intermediate in the field of organic synthesis, and to build reaction systems with the help of organic solvents to promote various chemical reactions. In water, its solubility is relatively limited, but it may change under certain conditions, such as increasing the temperature or adjusting the pH of the solution. This feature is of great significance in the field of drug research and development, which can adjust its dissolution according to needs to achieve effective drug delivery and release.
    When it comes to melting point, 2-% hydroxy-4-methyl-5-pyrimidinone has a clear melting point range. Accurate melting point data is critical to identify the compound and determine the purity. The melting point of high-purity 2-% hydroxy-4-methyl-5-pyrimidinone should be in a specific narrow range. If the melting point of the sample deviates from this range, or suggests the presence of impurities, further purification is required.
    In addition, there are specific functional groups in the 2-% hydroxy-4-methyl-5-pyrimidinone molecule, such as hydroxy and pyrimidinone structures, which give it a certain chemical activity. Hydroxyl groups have nucleophilic properties and can participate in substitution reactions, esterification reactions, etc.; pyrimidinone structure affects its overall electron cloud distribution and reactivity, which makes the compound exhibit unique reactive properties in the fields of organic synthesis and medicinal chemistry, and can be used to synthesize compounds with specific biological activities.
    What are the synthesis methods of 2-amino-4-methyl-5-nitropyridine?
    To prepare 2-amino-4-methyl-5-pyrimidinecarboxylic acid, there are many methods.
    First, it can be started by the corresponding pyrimidine derivative. Find a suitable pyrimidine compound containing methyl groups and groups that can be modified into amino and carboxyl groups. First, the modifiable groups are gradually converted with specific reagents and conditions. For example, halogenated pyrimidine derivatives, through nucleophilic substitution reaction, the amino group is introduced. Select an amine reagent with suitable nucleophilicity, and in the presence of a suitable solvent and base, the halogen atom is replaced by an amino group. Then, by suitable oxidation or other carboxylation means, the carboxyl group is introduced at the 5-position of the pyrimidine ring. This process requires fine control of reaction conditions, such as temperature, ratio of reactants, and reaction time, to avoid side reactions.
    Second, we can start from the construction of pyrimidine rings. Small molecule compounds containing methyl, amino and carboxyl precursors are used as raw materials to construct pyrimidine rings through condensation and cyclization reactions. For example, malonic acid derivatives and nitrogen-containing small molecules are used under the action of condensation agents and catalysts to conduct condensation reactions first and then cyclize to form pyrimidine rings. In this regard, the choice of malonic acid derivatives needs to take into account the convenience of subsequent introduction of methyl, amino and carboxyl groups. Condensation and cyclization conditions also need to be carefully explored. The polarity of the solvent, the type and dosage of the catalyst are all related to the success or failure of the reaction and the purity of the product.
    Third, biosynthetic pathways can also be used. Use the catalytic action of microorganisms or enzymes to achieve the synthesis of the target product under mild conditions. Microbial strains or enzymes that specifically catalyze the synthesis of 2-amino-4-methyl-5-pyrimidinecarboxylic acid for energy seeking. Through the optimization of microbial culture conditions, or the immobilization and modification of enzymes, the catalytic efficiency and selectivity can be improved. This biological method is green and environmentally friendly, but requires high technical requirements for bacterial species screening and culture, enzyme preparation and application.
    All synthetic methods have advantages and disadvantages. According to actual needs, factors such as raw material availability, cost, product purity, etc., the optimal method should be selected to prepare 2-amino-4-methyl-5-pyrimidinecarboxylic acid.
    What are the precautions for 2-amino-4-methyl-5-nitropyridine during storage and transportation?
    2-% Hydroxy-4-methyl-5-pyrimidinyl This substance requires attention to many matters during storage and transportation.
    First, when storing, be sure to ensure that the storage environment is dry and cool. Because the substance is in a humid environment, it is highly susceptible to moisture deterioration, which affects its chemical properties and quality. If moisture invades, it may cause structural changes, resulting in reduced activity or even loss of its due effectiveness. And if the temperature is too high, it may also promote chemical reactions, so it needs to be placed in a cool place to maintain its stability.
    Second, the storage place should be kept well ventilated. The substance may emit certain gases. If the ventilation is not smooth and the gas accumulates, it may pose a safety hazard and may also affect other substances stored around.
    Third, during transportation, the packaging must be solid and stable. Because of its specific chemical structure and properties, if the packaging is not strong, the bumps and vibrations during transportation are very likely to cause the packaging to be damaged and lead to material leakage. Once leaked, it will not only cause material damage, but also pose a threat to the transportation environment and personnel safety.
    Fourth, it must be strictly isolated from other chemical substances during transportation. The chemical properties of this substance may cause it to react with certain substances, such as contact with strong oxidants, strong acids and alkalis, etc., or it may cause violent reactions or even explosions, so it must be transported separately to avoid mixing.
    Fifth, whether it is storage or transportation, relevant personnel need to have a full understanding of the properties, hazards and emergency treatment methods of the substance. In the event of an unexpected situation, measures can be taken quickly and correctly to reduce losses and hazards.
    What are the effects of 2-amino-4-methyl-5-nitropyridine on the environment and human health?
    The effects of 2-% hydroxy-4-methyl-5-pyrimidinyl on the environment and human health have not been detailed in ancient times, but with today's scientific knowledge, it can be discussed.
    At the environmental end, if these compounds are released in nature, they may have complex effects on the ecosystem. They may accumulate in the soil, affecting the balance of soil microbial communities. Soil microorganisms are essential for soil fertility maintenance and material circulation. If their communities are disturbed, or cause abnormal soil nutrient transformation, affecting plant growth. And if they flow into water bodies, they may pose a threat to aquatic organisms. Aquatic organisms are sensitive to environmental changes, and this compound may interfere with their physiological processes, such as affecting the reproduction and development of fish, causing changes in population numbers, and then destroying the stability of aquatic ecology.
    As for human health, exposure to this compound also poses a latent risk. If it is ingested through respiration, skin contact or diet, or triggers a series of reactions in the body. Its structural properties may cause it to interact with human biological macromolecules, such as proteins and nucleic acids. Bind to proteins, or change the conformation and function of proteins, affecting the normal metabolism of cells. If it acts on nucleic acids, it may cause genetic mutations, increasing the risk of cancer. And long-term low-dose exposure may cause chronic health problems, such as weakened immune system function, making people more susceptible to diseases, nervous system involvement, and cognitive and behavioral abnormalities.
    Although there is no accurate description of this object in ancient times, according to current scientific understanding, its potential impact on the environment and human health should not be underestimated. It should be treated with caution, and monitoring and research should be strengthened to ensure the well-being of the environment and human beings.