4 Chloro 5 Nitro 2 Hydroxypyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-5-nitro-2-hydroxypyridine

    Specifications

    HS Code

    506592

    Name 4-Chloro-5-nitro-2-hydroxypyridine
    Molecular Formula C5H3ClN2O3
    Molecular Weight 174.54
    Appearance Solid (likely yellowish due to nitro group)
    Melting Point Data may vary, check literature
    Boiling Point Data may vary, check literature
    Solubility Solubility in water is likely low; may be more soluble in polar organic solvents
    Pka Related to phenolic -OH, data may vary
    Chemical Class Heterocyclic nitro - halogenated phenol - like compound
    Stability Can be reactive due to nitro and chloro groups; may be sensitive to reducing agents and strong bases
    Odor Odor may be faint and characteristic to the compound, details in literature

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    General Information
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    Frequently Asked Questions

    As a leading 4-Chloro-5-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 is the chemistry of 4-Chloro-5-nitro-2-hydroxypyridine?
    4-Chloro-5-nitro-2-hydroxypyridine is one of the organic compounds. It has unique chemical properties and has attracted much attention in the field of organic synthesis.
    Looking at its structure, chlorine atoms, nitro groups and hydroxyl groups coexist on the pyridine ring, and each atom interacts, giving this compound its specificity. Chlorine atoms have electron-absorbing effects, which can affect the electron cloud density of the pyridine ring, resulting in different chemical activities. Nitro is also a strong electron-absorbing group. The synergy between the two decreases the electron cloud density of the pyridine ring and increases the difficulty of electrophilic substitution reactions on the ring. However, in the nucleophilic substitution reaction, this structural change makes the pyridine ring more vulnerable to nucleophilic reagents. The hydroxyl group at the
    2-position can participate in many chemical reactions. It is acidic and can react with bases to form corresponding salts. And the hydroxyl group can be esterified and interact with acylating reagents to form ester compounds.
    Looking at its stability, the molecular energy state changes due to the strong electron-absorbing effect of chlorine and nitro. The presence of nitro groups expands the molecular conjugation system. Although it increases its stability, it also makes it more prone to react under certain conditions, such as the reduction reaction of nitro groups, which can be converted into amino groups.
    In chemical reactions, 4-chloro-5-nitro-2-hydroxypyridine can be used as a key intermediate. Its unique structure can introduce other functional groups through various reaction pathways to build complex organic molecules, which has potential application value in many fields such as medicinal chemistry and materials science.
    What are the common uses of 4-Chloro-5-nitro-2-hydroxypyridine?
    4-Chloro-5-nitro-2-hydroxypyridine, which has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of many specific drugs. Due to its specific chemical structure, it endows the drugs with unique pharmacological activities, or can participate in the creation of antibacterial and antiviral drugs, and achieve therapeutic effects by accurately acting on specific targets of pathogens.
    In the field of pesticide chemistry, it is also indispensable. It can be used as a raw material to synthesize pesticides with high insecticidal and bactericidal properties. With its structural characteristics, such pesticides are highly targeted to specific crop diseases and pests, and can effectively protect crop growth and improve agricultural yield and quality.
    In the field of materials science, 4-chloro-5-nitro-2-hydroxypyridine can be used to prepare special functional materials. By ingenious chemical reactions, it can be integrated into the material structure, or it can endow the material with special properties such as conductivity and optical activity, providing new possibilities for the development of electronic devices, optical materials and other fields.
    In addition, in organic synthetic chemistry, it is used as an important building block to participate in the construction of complex organic molecules. Chemists use its active functional groups to synthesize organic compounds with complex structures and special uses through various organic reactions, such as nucleophilic substitution, cyclization, etc., to promote the continuous development of organic synthetic chemistry. Overall, 4-chloro-5-nitro-2-hydroxypyridine plays a key role in many fields and is of great significance to the progress of related industries.
    What is 4-Chloro-5-nitro-2-hydroxypyridine synthesis method?
    The synthesis of 4-chloro-5-nitro-2-hydroxypyridine is quite delicate and requires specific steps and methods.
    When starting, suitable pyridine derivatives are often used as raw materials. The pyridine ring can be modified first to introduce the desired substituent. For example, a halogenation reaction can be used to introduce chlorine atoms at specific positions on the pyridine ring. This halogenation reaction requires the selection of suitable halogenation reagents, such as thionyl chloride, phosphorus oxychloride, etc., under appropriate reaction conditions, such as specific temperatures and solvent environments.
    After the chlorine atoms are successfully introduced, the nitrification reaction is continued. The nitration reaction also needs to be done carefully, and suitable nitration reagents should be selected, such as the mixed acid system of concentrated nitric acid and concentrated sulfuric acid. Strictly control the reaction temperature, time and other conditions, so that the nitro group can be precisely introduced into the target position of the pyridine ring, that is, the pyridine derivative containing chlorine and nitro group can be obtained.
    Then, for a certain substituent on the pyridine ring, the hydroxylation reaction is carried out. This step may require the use of a specific nucleophilic substitution reaction to react with the obtained derivative with a reagent containing hydroxyl groups. During the reaction process, factors such as the choice of solvent and the use of base have a great impact on the reaction process and yield. It is necessary to finely adjust the reaction conditions to promote the smooth progress of the reaction in the direction of generating 4-chloro-5-nitro-2-hydroxypyridine. After the reaction is completed, it needs to be separated and purified, such as column chromatography, recrystallization and other means to obtain high-purity target products. In this way, 4-chloro-5-nitro-2-hydroxypyridine can be obtained.
    4-Chloro-5-nitro-2-hydroxypyridine What are the precautions during storage and transportation?
    4-Chloro-5-nitro-2-hydroxypyridine, when storing and transporting, it is necessary to pay attention to many matters. This is due to the characteristics of the substance, which is related to the stability of its storage and transportation.
    First heavy packaging. The packaging must be tight and sealed to prevent it from contacting with outside air, moisture, etc. If the packaging is not tight, moisture will invade, or its properties will change, affecting the quality. For example, a wooden box must be solid and seamless, wrapped in multiple layers of oil paper, and then placed in the box.
    Times and environment. Store in a cool, dry and well-ventilated place. If the temperature is too high, it may cause chemical changes; if the humidity is too high, it is easy to deliquescence. And do not be in the same room with strong oxidants, strong acids and alkalis, because of their specific chemical activity, mixing with them may cause violent reactions and endanger safety.
    Further transportation. When handling, workers need to handle it with care and do not throw it roughly. During the journey, also ensure that the carrier is stable and free from bumps and vibrations. If transported by boat, keep the appropriate temperature and humidity in the compartment and cabin, and take measures to protect against wind and rain.
    In addition, marking is also key. Outside the packaging, indicate its product name, characteristics, danger warnings and other information with a prominent logo. In this way, whether it is the warehouser or the transporter, it can be seen at a glance and properly disposed of according to its characteristics.
    In short, the storage and transportation of 4-chloro-5-nitro-2-hydroxypyridine requires careful treatment at every step to ensure its safety and quality.
    4-Chloro-5-nitro-2-hydroxypyridine impact on the environment and human health
    4-Chloro-5-nitro-2-hydroxypyridine, this is a chemical substance. The impact on the environment and human health cannot be underestimated.
    Let's talk about the impact on the environment first. If this substance flows into the soil, or changes the chemical properties of the soil, it will cause soil fertility to become easier and affect plant growth. It may hinder the metabolism of soil microorganisms and disrupt the ecological balance of the soil. If it flows into the water body, it will also cause serious harm. It will change the chemical composition of the water body, causing aquatic organisms to face a crisis of survival. Aquatic animals such as fish and shellfish may be damaged due to their physiological functions, resulting in reproduction, growth inhibition, and even death. And because of its chemical stability, or long-term residual in the environment, it will accumulate continuously, and the harm will become more and more serious.
    As for the impact on human health, it cannot be ignored. Inhalation through the respiratory tract, skin contact, or accidental ingestion can endanger the human body. After entering the body, it may damage human organs. It may cause abnormal function of important organs such as the liver and kidneys. Its nitro, chlorine atom and other structures may be mutagenic, causing mutations in human cells and increasing the risk of cancer. Long-term exposure may affect the nervous system, causing headaches, dizziness, fatigue and other symptoms, interfering with the normal function of the nervous system.
    Therefore, 4-chloro-5-nitro-2-hydroxypyridine should be treated with caution to prevent it from causing disaster to the environment and human health.