4 Hydrazino 3 Nitropyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Hydrazino-3-nitropyridine

    Specifications

    HS Code

    217432

    Chemical Formula C5H6N4O2
    Appearance Solid (predicted)
    Melting Point No data available
    Boiling Point No data available
    Solubility In Water No data available
    Solubility In Organic Solvents No data available
    Density No data available
    Pka Value No data available
    Vapor Pressure No data available

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    General Information
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    Frequently Asked Questions

    As a leading 4-Hydrazino-3-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 4-Hydrazino-3-nitropyridine?
    4-Hydrazyl-3-nitropyridine is one of the organic compounds. Its main uses are in many fields.
    In the field of pharmaceutical chemistry, it is often used as a key intermediate for the synthesis of drugs. Due to its unique chemical structure, it can react with other compounds to build a molecular structure with biological activity. For example, when developing some new antibacterial drugs, 4-hydrazyl-3-nitropyridine can be used as a starting material to shape the core structure of the drug through a series of reaction steps, endowing the drug with antibacterial efficacy, and helping to deal with infections caused by specific bacteria.
    In the field of materials science, it is also of important value. Can participate in the synthesis of functional materials. For example, when synthesizing materials with special optical or electrical properties, it is introduced as a structural unit, which can adjust the molecular arrangement and electron cloud distribution of the material, and then endow the material with changes in fluorescence properties and electrical conductivity, providing the possibility for the development of new optoelectronic materials. It is expected to be applied to Light Emitting Diodes, sensors and other devices.
    In scientific research and exploration, it is also an important chemical reagent. Researchers use it to carry out various chemical reaction studies and explore new reaction pathways and reaction mechanisms. Due to the activity of hydrazine and nitro groups in the structure, it can trigger various reactions, contributing to the development of organic synthetic chemistry, pushing chemical science to continuously expand the cognitive boundaries and develop novel synthesis strategies and methods.
    What are the physical properties of 4-Hydrazino-3-nitropyridine?
    4-Hydrazine-3-nitropyridine is a kind of organic compound. Its physical properties are quite specific, let me tell them one by one.
    Looking at its appearance, at room temperature, it is mostly in a solid state, and it is often crystalline, like fine ice crystals, delicate and regular, and occasionally crystal clear under light.
    When it comes to the melting point, it is about a specific temperature range. This temperature value is the inherent characteristic of the compound, reflecting the stability of its lattice structure and the strength of intermolecular forces. When heated to this temperature, the lattice disintegrates, and the substance gradually melts from a solid state to a liquid state. This process is smooth and orderly, just like melting ice and melting snow, which is natural.
    The boiling point is also an important physical property. Under a specific pressure environment, when the temperature rises to the boiling point, 4-hydrazino-3-nitropyridine will change from a liquid state to a gaseous state, and the molecules will break free from the liquid phase and escape into space. The value of this boiling point is closely related to factors such as intermolecular interactions and molecular weight, acting as a threshold to define the transition of different phases of substances.
    In terms of solubility, 4-hydrazino-3-nitropyridine exhibits unique solubility properties in organic solvents. In some polar organic solvents, such as alcohols, there is a certain solubility, just like a fish entering water, and the molecules are evenly dispersed in it; in non-polar solvents, such as alkanes, the solubility is very small, just like oil and water, distinct. This difference in dissolution is due to the ratio and distribution of polar and non-polar groups in the molecular structure, which affects the interaction between them and different solvent molecules.
    The density is the mass of the substance per unit volume. The value reflects the compactness of the molecular packing, just like masonry building a wall, whether it is compact or not determines the density of the wall. The density of 4-hydrazine-3-nitropyridine is constant under certain conditions and is one of its inherent physical constants.
    The color of this compound is often light yellow or nearly colorless. Those who are pure have a light color, just like water. Only when crystallized with high purity, it may have a faint yellowish rhyme, just like the dim light of morning light, elegant but not public.
    Is 4-Hydrazino-3-nitropyridine chemically stable?
    The stability of the chemical properties of 4-hydrazine-3-nitropyridine is related to many aspects and cannot be generalized. The structure of this substance contains hydrazine group and nitro group, both of which have unique chemical activities and have a great impact on its stability.
    hydrazine group has strong reducing properties and is easy to react with oxidants. In air or in contact with oxidizing substances, hydrazine groups are easily oxidized, resulting in changes in molecular structure and impaired stability. For example, in contact with strong oxidants such as hydrogen peroxide, oxidation reactions can be rapidly initiated to form new substances.
    Nitro is an electron-absorbing group, which reduces the electron cloud density of the pyridine ring and enhances the stability of the ring. However, it is also active, and under specific conditions, it can undergo reactions such as reduction and substitution. For example, under the action of appropriate reducing agents, nitro groups can be reduced to amino groups, resulting in changes in molecular structure and properties.
    In addition, external conditions such as temperature and pH also have a significant impact on the stability of 4-hydrazine-3-nitropyridine. At high temperatures, molecular thermal motion intensifies, chemical reactivity increases, stability decreases, or reactions such as decomposition and rearrangement are triggered. In different pH media, its existence form and reactivity are different. Under acidic conditions, pyridine cyclic nitrogen atoms are easily protonated, which affects molecular stability and reactivity; under basic conditions, hydrazine groups are more active and easily react with other substances.
    In summary, the chemical stability of 4-hydrazino-3-nitropyridine is influenced by the characteristics of the groups in its own structure and external conditions, and it is not absolutely stable. It is prone to chemical changes under specific environments.
    What are 4-Hydrazino-3-nitropyridine synthesis methods?
    The synthesis methods of 4-hydrazine-3-nitropyridine are generally as follows.
    First, pyridine is used as the starting material. First, pyridine is made to meet the nitrate under specific conditions. After a delicate reaction, nitro is introduced at a specific position in the pyridine ring to obtain a nitro-containing pyridine derivative. Then, this derivative is co-located with a hydrazine reagent. In a suitable temperature, pH and other environments, the two interact. On the nitropyridine, the hydrazine group is successfully connected to the final 4-hydrazine-3-nitropyridine. In this process, the choice of reaction conditions is crucial. If the temperature is too high or too low, and the pH is slightly deviated, the yield and purity of the reaction may be affected.
    Second, there are also other nitrogen-containing heterocyclic compounds as starters. Such compounds are cleverly modified to have reactivity similar to that of pyridine derivatives. Nitro is introduced first, and then hydrazine is substituted to gradually build the structure of the target molecule. This path requires a thorough understanding of the chemical properties of the starter in order to accurately control each step of the reaction to achieve the purpose of synthesis.
    Third, there is a method of converting functional groups into the gist. Selecting pyridine derivatives with convertible functional groups, through a series of carefully designed reactions, the original functional groups are gradually converted into nitro and hydrazine groups. This process is like a delicate dance of chemistry. The sequence of reactions and the selection of reaction reagents need to be carefully considered. If you are not careful, you will easily go astray and it is difficult to obtain pure 4-hydrazine-3-nitropyridine.
    What is the price range of 4-Hydrazino-3-nitropyridine in the market?
    I have not obtained the exact price of 4-hydrazine-3-nitropyridine on the market. The price of this medicine may fluctuate due to changes in supply and demand, differences in manufacturing techniques, and differences in quality. To know the details, you should consult all chemical raw material suppliers, chemical reagent vendors, or on chemical trading platforms. This generation can tell the exact price according to the current market conditions. Or due to the quantity, the price is also different, and those who buy in bulk often get a good price. Therefore, if you want to know the exact price of 4-hydrazine-3-nitropyridine, you must consider the situation in detail, and those who consult carefully can only obtain it.