3 Nitro 2 Hydroxypyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Nitro-2-hydroxypyridine

    Specifications

    HS Code

    511955

    Chemical Formula C5H4N2O3
    Molecular Weight 140.1
    Appearance Solid
    Odor Unspecified
    Melting Point Unspecified
    Boiling Point Unspecified
    Solubility In Water Unspecified
    Solubility In Organic Solvents Unspecified
    Pka Unspecified
    Stability Unspecified
    Reactivity Unspecified
    Hazardous Nature Unspecified

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    General Information
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    Frequently Asked Questions

    As a leading 3-Nitro-2-hydroxypyridine 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 physical properties of 3-Nitro-2-hydroxypyridine?
    3-Nitro-2-hydroxypyridine is one of the organic compounds. Its physical properties are quite unique, so let me tell you in detail.
    When it comes to appearance, 3-nitro-2-hydroxypyridine is usually in a solid state. Its color may vary from light yellow to yellow. The appearance of this color is related to the functional groups such as nitro contained in the molecular structure. The presence of nitro groups affects the absorption and reflection of light by molecules, causing them to exhibit a specific color.
    As for the melting point, the melting point of this compound is also an important physical property. Generally speaking, its melting point is within a specific temperature range, which is of great significance for the identification and purification of this substance. By measuring the melting point, its purity can be verified. If it contains more impurities, the melting point will often change, or decrease, or the melting range will become wider.
    In terms of solubility, 3-nitro-2-hydroxypyridine behaves differently in different solvents. In organic solvents, such as ethanol, acetone, etc., it may have certain solubility. Due to the molecular structure of the compound, which contains both polar hydroxyl groups and polar pyridine rings and nitro groups, it can interact with some organic solvents through intermolecular forces to dissolve. However, the solubility in water is relatively limited, because the degree of matching between the polarity of water and the polarity of the compound is not completely consistent, and the hydrophobic effect of nitro and other groups in the molecule is also affected.
    In addition, its density is also one of the physical properties. The size of the density depends on its distribution and behavior in different media, and this property needs to be considered in practical applications, such as separation and mixing.
    In short, the physical properties of 3-nitro-2-hydroxypyridine, such as appearance, melting point, solubility and density, are related, and are of key significance in many fields such as chemical research and chemical production. Researchers can effectively separate, purify and apply it according to its physical properties.
    What are the chemical properties of 3-Nitro-2-hydroxypyridine?
    3-Nitro-2-hydroxypyridine, this is an organic compound, its chemical properties are particularly critical, and it has applications in many fields.
    It is acidic, and its phenolic hydroxyl group can release protons, which can react with bases to form corresponding salts. For example, in case of sodium hydroxide, sodium salts can be formed. This property is quite useful in organic synthesis. It can be used to separate and purify compounds by acid-base reaction, or to introduce specific functional groups.
    Its nitro nature is active, and the nitro group is a strong electron-absorbing group, which reduces the electron cloud density of the pyridine ring, which increases the difficulty of electrophilic substitution reaction on the ring, but it is prone to nucleophilic substitution reaction. For example, in the presence of nucleophiles, the carbon atoms in the ortho or para-nitro position are vulnerable to attack, and then new functional groups are introduced, which is an important strategy for building complex structures in organic synthesis.
    The compound also has certain redox properties. Nitro groups can be reduced under specific conditions, such as under the action of metal catalysts and hydrogen, nitro groups can be gradually converted into amino groups to obtain 3-amino-2-hydroxypyridine, which is an important step in the preparation of amino-containing compounds.
    In addition, the conjugated structure of 3-nitro-2-hydroxypyridine gives it certain optical properties, which may have potential applications in the field of photochemistry. It may exhibit specific absorption and emission spectra in solution, which can be used in optical sensors or fluorescent labeling.
    In conclusion, the diverse chemical properties of 3-nitro-2-hydroxypyridine make it important for research and application in many fields such as organic synthesis, medicinal chemistry, and materials science.
    What are the main uses of 3-Nitro-2-hydroxypyridine?
    3-Nitro-2-hydroxypyridine is one of the organic compounds. Its main uses are very wide.
    In the field of organic synthesis, it is a key intermediate. Chemists often use it to build complex organic molecules. For example, through specific chemical reactions, it can be converted into compounds with unique physiological activities, laying the foundation for drug development. In the process of drug development, it is necessary to create a variety of compounds to explore therapeutic potential. 3-nitro-2-hydroxypyridine can derive a variety of new structures due to its own structural characteristics, or can become a potential drug for the treatment of specific diseases.
    In the field of materials science, it also has extraordinary performance. It can be used to prepare materials with special properties. For example, in the synthesis of some functional polymer materials, the addition of this compound can change the electrical and optical properties of the material, making it suitable for specific needs in fields such as optoelectronics. For example, the manufacture of new light-emitting materials, or the improvement of the properties of semiconductor materials, etc., 3-nitro-2-hydroxypyridine may be used.
    In addition, in the field of chemical research, it is often used as a model compound. By studying its reaction characteristics, electronic structure, etc., scientists can gain in-depth insight into the mechanism of related chemical reactions and provide support for the development of broader chemical theories. Through in-depth investigation of it, the laws of many organic reactions can be revealed, thus guiding the synthesis and application of more organic compounds.
    What is 3-Nitro-2-hydroxypyridine synthesis method?
    To prepare 3-nitro-2-hydroxypyridine, the following method can be used.
    2-hydroxypyridine is often selected as the starting material. The structure of this compound lays the foundation for subsequent reactions. Its reaction step is the first denitrification reaction. When nitrifying, the reaction conditions and nitrification reagents should be carefully selected.
    Common nitrification reagents, such as the mixed acid system of concentrated nitric acid and concentrated sulfuric acid. This mixed acid system can effectively provide nitro positive ions and is the key active species in the nitrification reaction. 2-Hydroxypyridine is slowly added to the pre-cooled mixed acid system because the nitrification reaction is violent and exothermic. Slow addition can effectively control the temperature and avoid side reactions. And the low temperature environment, generally controlled at 0-5 ° C, helps the reaction to proceed in the direction of generating the target product.
    The reaction process needs to be closely monitored. The reaction can be tracked by thin layer chromatography (TLC) to determine the reaction process and endpoint. After the reaction is completed, post-processing operations are required. When
    is post-treated, the reaction mixture is poured into ice water, so that the product can be precipitated from the system, or by extraction, the product can be extracted from the aqueous phase with a suitable organic solvent, such as ethyl acetate, etc. Subsequently, the organic phase is dried with a desiccant such as anhydrous sodium sulfate to remove the moisture.
    Finally, the product is purified by means of vacuum distillation and column chromatography. During column chromatography purification, suitable silica gel and eluent are selected, which can effectively separate impurities and obtain a pure 3-nitro-2-hydroxypyridine product. The whole synthesis process, the control of reaction conditions, the selection of reagents and the fineness of post-processing operations are all the keys to obtaining high-purity products.
    What are the precautions in storage and transportation of 3-Nitro-2-hydroxypyridine?
    For 3-nitro-2-hydroxypyridine, many matters need to be paid attention to during storage and transportation.
    Its properties are chemical substances, and when storing, the first choice is the environment. It should be placed in a cool, dry and well-ventilated place, away from fires and heat sources. This is because the substance is heated or exposed to open flames, it is dangerous, such as the risk of combustion or even explosion.
    Furthermore, it needs to be stored separately from oxidants, reducing agents, acids, bases, etc., and must not be mixed. Because of its active chemical properties, contact with the above-mentioned substances is prone to chemical reactions, causing changes in composition, or generating harmful substances.
    Packaging is also crucial. Appropriate packaging materials must be used to ensure a good seal to prevent leakage. If the packaging is damaged, not only the product is easy to deteriorate, but also leaks or pollutes the environment, endangering personal safety.
    During transportation, the same cannot be slack. The transportation vehicle must be equipped with the corresponding variety and quantity of fire protection equipment and leakage emergency treatment equipment. When driving, the driver should drive slowly to avoid bumps and vibrations and prevent damage to the packaging.
    During loading and unloading, it should be handled lightly. It is strictly forbidden to drop, touch or collide, so as not to damage the packaging and cause danger. The escort personnel also need to supervise the whole process to ensure the safety of transportation. In this way, 3-nitro-2-hydroxypyridine can be stored and transported to maintain its quality and avoid disasters.