3 Chloro 5 Bromopyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Chloro-5-bromopyridine

    Specifications

    HS Code

    304718

    Chemical Formula C5H3BrClN
    Molecular Weight 192.44
    Appearance Typically a solid
    Physical State At Room Temp Solid
    Melting Point Varies (needs experimental determination)
    Boiling Point Varies (needs experimental determination)
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
    Density Needs experimental determination
    Odor Unpleasant odor likely
    Stability Stable under normal conditions but may react with strong oxidizing agents
    Flash Point Needs experimental determination
    Hazard Class Irritant (can cause eye, skin and respiratory irritation)

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    Frequently Asked Questions

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    What are the physical properties of 3-Chloro-5-bromopyridine?
    3-Chloro-5-bromopyridine is a kind of organic compound. Its physical properties are particularly important and are related to the basis of many chemical applications.
    First of all, its appearance is usually a colorless to pale yellow liquid or crystalline state. The appearance of this state often depends on the temperature and humidity of the surrounding environment and other factors. Looking at its color, its light yellow color is like the shimmer of morning light, soft and showing its characteristics.
    As for the melting point, the melting point is about [specific melting point value], and the boiling point is about [specific boiling point value]. At the melting point, the state of matter is solid and liquid, like ice and snow melting, following the laws of physics. At the boiling point, the liquid boils into a gaseous state, such as the rising of clouds. These two points are its key physical characteristics, which can guide the experimental operation of separation and purification, and even the process of industrial production.
    Its density is also fixed, about [specific density value] g/cm ³, which determines its floating and sinking situation in the liquid system. If a boat is traveling in water, the density is different, resulting in its location. And it has a certain solubility. It is soluble and miscible in organic solvents such as ethanol and ether, but its solubility in water is relatively limited. This characteristic comes from the difference between its molecular structure and the forces between water molecules and organic solvent molecules. Just like the difference between interpersonal affinity and sparsity, the molecules are also miscible or not due to the difference in structure.
    The vapor pressure of 3-chloro-5-bromopyridine is also a fixed value at a specific temperature, which is related to its volatility. If the vapor pressure is high, it will be volatile, such as the smell of incense and the level of vapor pressure, which affects the rate of diffusion in the air.
    In addition, its refractive index is also characterized, which is about [specific refractive index value]. This value is an important basis for identifying this object in optical analysis and related research. Light is refracted in it, like light passing through different media and experiencing a wonderful change. Refractive index is the parameter for recording this change.
    In summary, the physical properties of 3-chloro-5-bromopyridine, such as appearance, melting point, density, solubility, vapor pressure, and refractive index, are characteristic of each other and are related to each other. In the field of chemical research and practical application, it is the cornerstone for exploring its properties and exerting its effectiveness.
    What are the chemical properties of 3-Chloro-5-bromopyridine?
    3-Chloro-5-bromopyridine is an organic compound, and its chemical properties are particularly important.
    In this compound, both chlorine and bromine are halogen atoms, giving them unique reactivity. As far as nucleophilic substitution is concerned, halogen atoms can be replaced by many nucleophilic reagents. Edge halogen atoms are electron-absorbing, which reduces the electron cloud density on the pyridine ring, especially the adjacent and para-position of halogen atoms, so nucleophilic reagents are easy to attack these positions. For example, when encountering hydroxyl negative ions (OH), under suitable conditions, chlorine or bromine atoms can be replaced by hydroxyl groups to form corresponding hydroxypyridine derivatives.
    Because of the aromatic nature of the pyridine ring, aromatic electrophilic substitution reactions can occur. However, due to the electron-withdrawing effect of chlorine and bromine, the reactivity is slightly lower than that of the benzene ring. Under certain conditions, it can react with electrophilic reagents such as nitro-positive ions (NO ²) to introduce nitro groups on the pyridine ring.
    In addition, 3-chloro-5-bromopyridine can also participate in metal-catalyzed coupling reactions. Like palladium catalyzed, Suzuki coupling reactions can occur with borate esters to form new carbon-carbon bonds and generate more complex organic compounds. Due to the presence of halogen atoms in its structure, 3-chloro-5-bromopyridine is often used as a key intermediate in the field of organic synthesis for the preparation of various drugs, pesticides and functional materials containing pyridine structures. It plays an indispensable role in many fields.
    What are the main uses of 3-Chloro-5-bromopyridine?
    3-Chloro-5-bromopyridine is a crucial intermediate in the field of organic synthesis. It has a wide range of uses and has significant functions in many aspects such as medicine, pesticides, and materials.
    In the synthesis of medicine, this compound is often a key starting material. Due to its unique structure, it can be used for a variety of organic reactions to construct complex molecular structures with biological activity. For example, through nucleophilic substitution reactions, various functional groups, such as amino groups and hydroxyl groups, can be introduced to create drugs for specific diseases. New compounds with anti-tumor activity have been synthesized by using 3-chloro-5-bromopyridine as a base, which can precisely act on specific targets of tumor cells and inhibit the proliferation and metastasis of tumor cells.
    In the field of pesticides, this also has extraordinary uses. It can be chemically modified to synthesize pesticides with high insecticidal, bactericidal or herbicidal activities. Because its pyridine ring structure gives the compound certain stability and biological activity, it can be cleverly designed to make the pesticide more selective and durable. For example, a new type of insecticide synthesized with 3-chloro-5-bromopyridine as a raw material shows excellent toxic effect on specific pests, and has little impact on the environment.
    Furthermore, in the field of materials science, 3-chloro-5-bromopyridine can be involved in the preparation of special functional materials. For example, after polymerization, it is introduced into the polymer structure, giving the material unique electrical, optical or thermal properties. The resulting optoelectronic materials may emerge in the fields of organic Light Emitting Diodes (OLEDs) and solar cells, opening up new paths for the research and development of new materials.
    In summary, although 3-chloro-5-bromopyridine is an organic small molecule, it plays an indispensable role in many fields of modern chemical industry. With its unique structure and diverse chemical transformations, it has derived many products with practical value, promoting the progress and development of medicine, pesticides, materials and other industries.
    What are 3-Chloro-5-bromopyridine synthesis methods?
    3-Chloro-5-bromopyridine is also an important intermediate in organic synthesis. The synthesis method has been explored by many predecessors, and the common ones are listed below.
    First, pyridine is used as the starting material and brominated first to obtain bromopyridine. The nitrogen atom of capyridine has an electron-absorbing effect, which reduces the electron cloud density of the pyridine ring. However, under appropriate conditions, bromine can selectively replace the hydrogen atom at a specific position on the pyridine ring. For example, under a catalyst and a specific reaction temperature, bromine can be substituted at the 3-position or 5-position of the pyridine ring. Then chlorination is carried out, and chlorine atoms are introduced into the brominated pyridine to obtain 3-chloro-5-bromopyridine. This process requires fine regulation of the reaction conditions, because the selectivity and degree of reaction between bromination and chlorination affect the purity and yield of the final product.
    Second, nitrogen-containing heterocyclic compounds are used as raw materials and synthesized through multi-step reactions. For example, a specific nitrogen-containing fused ring or heterocyclic ring structure is selected and functionalized to construct a structural unit similar to the pyridine ring. Then through a suitable reaction, bromine and chlorine atoms are gradually introduced, and the pyridine ring is constructed through cyclization and other steps, and the position of bromine and chlorine is precisely positioned, and finally 3-chloro-5-bromopyridine is obtained. Although there are many steps in this route, the selectivity and yield of the target product can be improved by reasonably designing the reaction path, and the requirements for the reaction conditions are more stringent. The temperature, the proportion of reactants and the amount of catalyst in each step of the reaction need to be strictly controlled.
    Third, the cross-coupling reaction using metal catalysis is used. Halogenated pyridine derivatives are used as substrates, and transition metal catalysts, such as palladium and nickel, are used to cross-couple with bromine and chlorine-containing reagents. In this process, the metal catalyst can activate the substrate molecules, promote the cracking of carbon-halogen bonds and couple with the corresponding reagents, so as to achieve the precise introduction of bromine and chlorine atoms on the pyridine ring. The reaction conditions of this method are relatively mild and the selectivity is high, but the cost of the metal catalyst is high, and the separation and recovery of the catalyst after the reaction are also issues to be considered.
    The above synthesis methods have advantages and disadvantages. In practical applications, the most suitable method is selected to synthesize 3-chloro-5-bromopyridine according to the availability of raw materials, the difficulty of controlling the reaction conditions, the purity of the product, and the cost.
    What 3-Chloro-5-bromopyridine need to pay attention to when storing and transporting
    3-Chloro-5-bromopyridine is one of the organic compounds. When storing and transporting, many matters must be paid attention to.
    Let's talk about storage first. This compound may be active in nature, so it should be stored in a cool, dry and well-ventilated place. Because it is easy to cause chemical reactions due to heat, it must be kept away from fire and heat sources to prevent accidents. And because it may be toxic and corrosive, the storage place must be stored separately from oxidants, acids, alkalis and other substances, and must not be mixed to avoid danger caused by interaction. Storage containers are also crucial, and corrosion-resistant materials must be selected and tightly sealed to prevent leakage.
    As for transportation, the first thing to ensure is that the packaging is complete and sealed. During transportation, the vehicle should be equipped with the corresponding variety and quantity of fire protection equipment and leakage emergency treatment equipment. When driving, avoid exposure to the sun, rain, and high temperature. During transportation, you should follow the specified route and do not stop in residential areas and densely populated areas. When handling, you should pack and unload lightly to prevent damage to packaging and containers. If a leak occurs during transportation, you should quickly evacuate the personnel from the leaked contaminated area to a safe area and isolate them, strictly restricting access. Emergency personnel must wear self-contained positive pressure breathing apparatus, wear anti-toxic clothing, and do not directly contact leaks. Small leaks can be absorbed by sand, vermiculite or other inert materials; large leaks need to be built embankments or dug for containment, pumped to a tanker or special collector, recycled or transported to a waste disposal site for disposal.
    All of these are to be carefully paid attention to when storing and transporting 3-chloro-5-bromopyridine, so as to ensure safety and avoid accidents.