Linshang Chemical
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2,6-Dibromochlorobenzene
Linshang Chemical
|
HS Code |
707562 |
| Chemical Formula | C6H3Br2Cl |
| Molar Mass | 270.35 g/mol |
| Appearance | White to off - white solid |
| Melting Point | 39 - 41 °C |
| Boiling Point | 244 - 246 °C |
| Density | 2.07 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
| Vapor Pressure | Low |
| Odor | Faint, characteristic |
As an accredited 2,6-Dibromochlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2,6 - dibromochlorobenzene packaged in a sealed glass bottle. |
| Storage | 2,6 - dibromochlorobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly - sealed container to prevent vapor leakage. Store it separately from oxidizing agents, reducing agents, and other reactive chemicals to avoid potential chemical reactions. |
| Shipping | 2,6 - dibromochlorobenzene should be shipped in well - sealed containers, following hazardous chemical regulations. It must be protected from heat, direct sunlight, and stored away from incompatible substances during transit. |
Competitive 2,6-Dibromochlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,6-Dibromochlorobenzene in China?
As a trusted 2,6-Dibromochlorobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 2,6-Dibromochlorobenzene 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 2,6-dibromochlorobenzene?
2% 2C6-dibromonaphthalene is an important raw material for organic synthesis and has significant uses in many fields.
First, in the field of materials science, it is often a key monomer for the synthesis of high-performance polymers. Polymer materials with excellent thermal stability, mechanical properties and flame retardant properties can be prepared through specific polymerization reactions. These materials are widely used in electronic appliances, aerospace and other industries, such as packaging materials for electronic equipment and structural components of aerospace vehicles, providing reliable performance guarantees for related products.
Second, in the field of medicinal chemistry, 2% 2C6-dibromonaphthalene also plays an indispensable role. Using it as a starting material, through a series of organic synthesis steps, compounds with unique biological activities can be constructed. After in-depth research and development, these compounds can become potential drugs for the treatment of specific diseases and contribute to the development of human health.
Third, in the dye industry, 2% 2C6-dibromonaphthalene plays an important role. On this basis, dyes with brilliant colors and good stability can be synthesized. Such dyes are widely used in textiles, printing and dyeing and other industries to impart rich, diverse and lasting bright colors to fabrics, meeting people's needs for beautiful clothing and decorative fabrics.
To sum up, 2% 2C6-dibromonaphthalene plays an important role in many industries such as materials, medicine, dyes, etc., and is of great significance in promoting technological progress and product upgrades in various industries.
First, in the field of materials science, it is often a key monomer for the synthesis of high-performance polymers. Polymer materials with excellent thermal stability, mechanical properties and flame retardant properties can be prepared through specific polymerization reactions. These materials are widely used in electronic appliances, aerospace and other industries, such as packaging materials for electronic equipment and structural components of aerospace vehicles, providing reliable performance guarantees for related products.
Second, in the field of medicinal chemistry, 2% 2C6-dibromonaphthalene also plays an indispensable role. Using it as a starting material, through a series of organic synthesis steps, compounds with unique biological activities can be constructed. After in-depth research and development, these compounds can become potential drugs for the treatment of specific diseases and contribute to the development of human health.
Third, in the dye industry, 2% 2C6-dibromonaphthalene plays an important role. On this basis, dyes with brilliant colors and good stability can be synthesized. Such dyes are widely used in textiles, printing and dyeing and other industries to impart rich, diverse and lasting bright colors to fabrics, meeting people's needs for beautiful clothing and decorative fabrics.
To sum up, 2% 2C6-dibromonaphthalene plays an important role in many industries such as materials, medicine, dyes, etc., and is of great significance in promoting technological progress and product upgrades in various industries.
What are the physical properties of 2,6-dibromochlorobenzene?
2% 2C6-dibromo-p-cresol, an organic compound. It has the following physical properties:
Viewed, at room temperature, this substance is mostly white to light yellow crystalline powder, with fine texture, uniform particles visible visually, a certain luster on the surface, and a slightly reflective state under light.
Smell, with a special smell of organic bromide, although not pungent and intolerable, but under a fine smell, it is also different from common odorless substances. This smell can be used as a preliminary identification feature.
In terms of its melting and boiling point, the melting point is about 66-68 ° C. When the temperature rises to this point, 2% 2C6-dibromo-p-cresol in the solid state will gradually melt into a liquid state; the boiling point is relatively high, about 256 ° C. At this high temperature, the substance changes from a liquid state to a gaseous state and dissipates.
As for solubility, it is slightly soluble in water and difficult to disperse and dissolve in water, just like a water-repellent state; however, most organic solvents, such as ethanol, ether, acetone, etc., have good solubility and can quickly melt with organic solvents to form a uniform solution.
In terms of density, it is heavier than water. When placed in water, it will slowly sink to the bottom of the water. This characteristic is also one of its physical properties.
To sum up, the physical properties of 2% 2C6-dibromo-p-cresol, from appearance, odor, melting point, solubility to density, are unique, which is the cornerstone of in-depth understanding and application of this substance.
Viewed, at room temperature, this substance is mostly white to light yellow crystalline powder, with fine texture, uniform particles visible visually, a certain luster on the surface, and a slightly reflective state under light.
Smell, with a special smell of organic bromide, although not pungent and intolerable, but under a fine smell, it is also different from common odorless substances. This smell can be used as a preliminary identification feature.
In terms of its melting and boiling point, the melting point is about 66-68 ° C. When the temperature rises to this point, 2% 2C6-dibromo-p-cresol in the solid state will gradually melt into a liquid state; the boiling point is relatively high, about 256 ° C. At this high temperature, the substance changes from a liquid state to a gaseous state and dissipates.
As for solubility, it is slightly soluble in water and difficult to disperse and dissolve in water, just like a water-repellent state; however, most organic solvents, such as ethanol, ether, acetone, etc., have good solubility and can quickly melt with organic solvents to form a uniform solution.
In terms of density, it is heavier than water. When placed in water, it will slowly sink to the bottom of the water. This characteristic is also one of its physical properties.
To sum up, the physical properties of 2% 2C6-dibromo-p-cresol, from appearance, odor, melting point, solubility to density, are unique, which is the cornerstone of in-depth understanding and application of this substance.
What are the chemical properties of 2,6-dibromochlorobenzene?
2% 2C6-dibromonaphthalene is one of the organic compounds. Its properties are unique, let me come to you.
The color state of this compound, at room temperature, is often white to pale yellow crystalline. Looking at its physical characteristics, the melting point is quite high, about 80 to 8 degrees Celsius. The boiling point is also considerable, around 360 degrees Celsius. Its density is higher than that of water, and it is difficult to dissolve in water, but it can be soluble in many organic solvents, such as ethanol, ether, benzene, etc.
In terms of chemical properties, the structure of the naphthalene ring in 2% 2C6-dibromonaphthalene gives it aromatic properties. The presence of bromine atoms makes this compound have the characteristics of halogenated hydrocarbons. First, nucleophilic substitution reactions can occur. When encountering nucleophilic reagents, bromine atoms can be replaced by nucleophilic groups. For example, if treated with an aqueous solution of sodium hydroxide, with the help of appropriate temperatures and catalysts, bromine atoms can be replaced by hydroxyl groups to generate 2% 2C6-dihydroxynaphthalene. Second, it can participate in the elimination reaction. Under strong bases and appropriate conditions, bromine atoms and hydrogen atoms on adjacent carbons can debromide hydrogen to form an unsaturated double bond structure, and then form ethylenically bonded naphthalene derivatives. Third, due to the activity of naphthalene rings, 2% 2C6-dibromonaphthalene can also undergo aromatic electrophilic substitution reactions. Such as mixed acid with concentrated sulfuric acid and concentrated nitric acid, nitro groups can be introduced at specific positions in the naphthalene ring to generate nitro-substituted 2% 2C6-dibromonaphthalene derivatives.
In addition, 2% 2C6-dibromonaphthalene is widely used in the field of organic synthesis. It can be used as an intermediate to prepare various functional organic materials and pharmaceutical intermediates through a series of reactions.
The color state of this compound, at room temperature, is often white to pale yellow crystalline. Looking at its physical characteristics, the melting point is quite high, about 80 to 8 degrees Celsius. The boiling point is also considerable, around 360 degrees Celsius. Its density is higher than that of water, and it is difficult to dissolve in water, but it can be soluble in many organic solvents, such as ethanol, ether, benzene, etc.
In terms of chemical properties, the structure of the naphthalene ring in 2% 2C6-dibromonaphthalene gives it aromatic properties. The presence of bromine atoms makes this compound have the characteristics of halogenated hydrocarbons. First, nucleophilic substitution reactions can occur. When encountering nucleophilic reagents, bromine atoms can be replaced by nucleophilic groups. For example, if treated with an aqueous solution of sodium hydroxide, with the help of appropriate temperatures and catalysts, bromine atoms can be replaced by hydroxyl groups to generate 2% 2C6-dihydroxynaphthalene. Second, it can participate in the elimination reaction. Under strong bases and appropriate conditions, bromine atoms and hydrogen atoms on adjacent carbons can debromide hydrogen to form an unsaturated double bond structure, and then form ethylenically bonded naphthalene derivatives. Third, due to the activity of naphthalene rings, 2% 2C6-dibromonaphthalene can also undergo aromatic electrophilic substitution reactions. Such as mixed acid with concentrated sulfuric acid and concentrated nitric acid, nitro groups can be introduced at specific positions in the naphthalene ring to generate nitro-substituted 2% 2C6-dibromonaphthalene derivatives.
In addition, 2% 2C6-dibromonaphthalene is widely used in the field of organic synthesis. It can be used as an intermediate to prepare various functional organic materials and pharmaceutical intermediates through a series of reactions.
What are the synthesis methods of 2,6-dibromochlorobenzene?
The synthesis method of 2% 2C6-dibromonaphthalene is very subtle. In the past, all the wise men worked hard in the field of organic synthesis and obtained many good methods.
One method is to use naphthalene as the base and borrow the technique of bromination. Naphthalene has aromatic ring properties and has different chemical activities. The naphthalene is placed in an appropriate solvent, such as glacial acetic acid, and an appropriate amount of bromine is added, followed by a catalyst, such as iron powder. When bromine encounters naphthalene, under the impetus of the catalyst, an electrophilic substitution reaction occurs. The bromine atom gradually enters the ring naphthalene. After delicate regulation, the bromine atom can be preferably occupied at the 2,6-position, and then 2,6-dibromonaphthalene is obtained. In this process, temperature, amount of bromine, and reaction time are all key. If the temperature is high, the reaction will be too fast and by-products will be produced easily; if the temperature is low, the reaction will be slow and the yield will not be high. The amount of bromine also needs to be accurate. If the excess is too much, the polybromide will be clustered, and if it is not enough, the product will be impure.
There is another way to functionalize the naphthalene ring first. Starting with naphthalene, introduce groups that can activate the naphthalene ring and have localization effects, such as methoxy groups. Methoxy groups can change the electron cloud density distribution of the naphthalene ring, making it easier for bromine atoms to tend to specific positions during subsequent bromination. After the localization group is introduced, the bromination reaction is carried out. After the bromination is completed, try to remove the positioning group and convert it in multiple steps to obtain 2,6-dibromonaphthalene. Although this method is slightly complicated, the purity of the product is quite high and the yield is also good.
There are also those who use naphthalene derivatives as raw materials. Find a naphthalene derivative with a suitable substituent, and its substitution is based on the direction of the bromine atom in the reaction. Through ingenious design, the bromination reaction is directed to occur at the 2,6-position. This approach requires careful consideration of the structure of the raw material derivative and selection of the appropriate raw material to make the reaction smooth and the product satisfactory. In the process of synthesis, various methods have their own advantages and disadvantages, and they need to be weighed according to actual needs to achieve the best synthetic effect.
One method is to use naphthalene as the base and borrow the technique of bromination. Naphthalene has aromatic ring properties and has different chemical activities. The naphthalene is placed in an appropriate solvent, such as glacial acetic acid, and an appropriate amount of bromine is added, followed by a catalyst, such as iron powder. When bromine encounters naphthalene, under the impetus of the catalyst, an electrophilic substitution reaction occurs. The bromine atom gradually enters the ring naphthalene. After delicate regulation, the bromine atom can be preferably occupied at the 2,6-position, and then 2,6-dibromonaphthalene is obtained. In this process, temperature, amount of bromine, and reaction time are all key. If the temperature is high, the reaction will be too fast and by-products will be produced easily; if the temperature is low, the reaction will be slow and the yield will not be high. The amount of bromine also needs to be accurate. If the excess is too much, the polybromide will be clustered, and if it is not enough, the product will be impure.
There is another way to functionalize the naphthalene ring first. Starting with naphthalene, introduce groups that can activate the naphthalene ring and have localization effects, such as methoxy groups. Methoxy groups can change the electron cloud density distribution of the naphthalene ring, making it easier for bromine atoms to tend to specific positions during subsequent bromination. After the localization group is introduced, the bromination reaction is carried out. After the bromination is completed, try to remove the positioning group and convert it in multiple steps to obtain 2,6-dibromonaphthalene. Although this method is slightly complicated, the purity of the product is quite high and the yield is also good.
There are also those who use naphthalene derivatives as raw materials. Find a naphthalene derivative with a suitable substituent, and its substitution is based on the direction of the bromine atom in the reaction. Through ingenious design, the bromination reaction is directed to occur at the 2,6-position. This approach requires careful consideration of the structure of the raw material derivative and selection of the appropriate raw material to make the reaction smooth and the product satisfactory. In the process of synthesis, various methods have their own advantages and disadvantages, and they need to be weighed according to actual needs to achieve the best synthetic effect.
What are the precautions for storing and transporting 2,6-dibromochlorobenzene?
2% 2C6-dichlorotoluene is one of the organic compounds. When storing and transporting, pay attention to many matters.
First, when storing, choose a cool and ventilated warehouse. This is because the substance is easily dangerous when heated. If the temperature of the warehouse is too high, or it may cause a chemical reaction, resulting in a safety accident. And it must be kept away from fires and heat sources. Because 2% 2C6-dichlorotoluene is flammable, it is easy to burn and explode in case of open flames and hot topics. When the lighting, ventilation and other facilities of the warehouse are explosion-proof, the switch should be placed outside the warehouse to prevent accidents caused by electric sparks.
Second, it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed.
Third, when transporting, it is necessary to ensure that the container does not leak, collapse, fall, or damage. Because if it leaks, it will not only pollute the environment, but also the volatile gas will endanger human health, and there is also a risk of explosion in case of open fire. Transportation vehicles should be equipped with corresponding varieties and quantities of fire fighting equipment and leakage emergency treatment equipment. In summer, it should be transported in the morning and evening to avoid high temperature periods to reduce the possibility of volatilization and reaction due to temperature rise. During transportation, it should be protected from sun exposure, rain and high temperature. Road transportation should follow the specified route and do not stop in residential areas and densely populated areas.
Fourth, whether it is storage or transportation, operators should be specially trained and strictly abide by the operating procedures. When operating, you should wear a self-priming filter gas mask (half mask), chemical safety glasses, anti-poison penetration overalls, and rubber oil-resistant gloves to protect yourself.
First, when storing, choose a cool and ventilated warehouse. This is because the substance is easily dangerous when heated. If the temperature of the warehouse is too high, or it may cause a chemical reaction, resulting in a safety accident. And it must be kept away from fires and heat sources. Because 2% 2C6-dichlorotoluene is flammable, it is easy to burn and explode in case of open flames and hot topics. When the lighting, ventilation and other facilities of the warehouse are explosion-proof, the switch should be placed outside the warehouse to prevent accidents caused by electric sparks.
Second, it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed.
Third, when transporting, it is necessary to ensure that the container does not leak, collapse, fall, or damage. Because if it leaks, it will not only pollute the environment, but also the volatile gas will endanger human health, and there is also a risk of explosion in case of open fire. Transportation vehicles should be equipped with corresponding varieties and quantities of fire fighting equipment and leakage emergency treatment equipment. In summer, it should be transported in the morning and evening to avoid high temperature periods to reduce the possibility of volatilization and reaction due to temperature rise. During transportation, it should be protected from sun exposure, rain and high temperature. Road transportation should follow the specified route and do not stop in residential areas and densely populated areas.
Fourth, whether it is storage or transportation, operators should be specially trained and strictly abide by the operating procedures. When operating, you should wear a self-priming filter gas mask (half mask), chemical safety glasses, anti-poison penetration overalls, and rubber oil-resistant gloves to protect yourself.
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