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2,6-Difluorobenzene

2,6-Difluorobenzene

Hongda Chemical

Specifications

HS Code

674668

Chemical Formula C6H4F2
Molecular Weight 114.09
Appearance Colorless liquid
Boiling Point 102 - 103 °C
Melting Point -34.8 °C
Density 1.227 g/mL at 25 °C
Vapor Pressure 13.33 kPa (25.3 °C)
Solubility In Water Insoluble
Flash Point 12 °C
Odor Characteristic aromatic odor

As an accredited 2,6-Difluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 250 - gram bottle packaging for 2,6 - difluorobenzene chemical.
Storage 2,6 - difluorobenzene should be stored in a cool, well - ventilated area, away from heat sources and open flames as it is flammable. Keep the container tightly closed to prevent vapor leakage. Store it in a place separate from oxidizing agents to avoid potential chemical reactions. Use appropriate storage cabinets or areas compliant with safety regulations to ensure safe storage.
Shipping 2,6 - difluorobenzene is shipped in tightly sealed, corrosion - resistant containers. It's transported by specialized chemical carriers, ensuring compliance with safety regulations to prevent spills and exposure during transit.
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2,6-Difluorobenzene 2,6-Difluorobenzene
General Information
Historical Development
The industry of chemical industry is changing with each passing day, and all kinds of products have their own sources. In today's words, 2,6-difluorobenzene, in the past, at the beginning, the road to research and development has been difficult to prepare.
At the beginning, everyone explored in the field of chemistry, wanting new things to meet all needs. The wise men worked hard, and after countless trials, they obtained this 2,6-difluorobenzene. At the beginning, the preparation method was still simple, and the yield was quite small, but everyone was not discouraged.
With the passage of time, science and technology are advancing day by day, and the preparation technology is also becoming more and more exquisite. Many scholars have learned from others' strengths and improved their techniques, so that their yield has gradually increased and the quality has become better. Therefore, 2,6-difluorobenzene is involved in a wide range of chemical industries, and it is a thing that the industry relies on. Its development path is like the beginning of the stars, gradually shining.
Product Overview
2,6-Difluorobenzene is an organic compound. It is a colorless liquid with a special odor. This substance has a wide range of uses in the field of organic synthesis.
Its preparation method is often obtained by a specific halogenation reaction. By carefully adjusting the reaction conditions, such as temperature, ratio of reagents, etc., the reaction can proceed smoothly to obtain a higher yield.
2,6-difluorobenzene is an important intermediate in medicinal chemistry. It can help synthesize a variety of specific drugs to cure various diseases. In the field of materials science, it also has its unique applications, which can contribute to the research and development of new materials.
From the perspective of its chemical properties, it has considerable stability, but under specific circumstances, it can also exhibit active reactivity, and undergo delicate chemical reactions with a variety of reagents, resulting in a variety of products. This is of great significance in the process of chemical research.
Physical & Chemical Properties
2,6-Difluorobenzene is a chemical product. It has unique physical and chemical properties. Looking at its physical properties, at room temperature, it is mostly a colorless liquid with a clear odor and certain volatility. Its boiling point and melting point are the keys to characterizing physical properties.
On chemical properties, the introduction of 2,6-difluorobenzene fluorine atoms makes its chemical activity different from that of benzene. Fluorine has strong electronegativity, which changes the electron cloud density of the benzene ring, and shows different activity and selectivity in reactions such as electrophilic substitution. It may participate in various reactions such as halogenation and alkylation, and is of great value in the field of organic synthesis. It is an important raw material for the synthesis of many fine chemicals and drugs, and has made significant contributions to the process of the chemical industry.
Technical Specifications & Labeling
In this research on 2,6-difluorobenzene, its technical specifications and identification (product parameters) are the key. For 2,6-difluorobenzene, the color is pure and the quality is pure, and there should be no variegated odor. Its purity needs to reach a very high standard, and the impurity content must be minimal. Looking at its shape, it should be stable at room temperature.
In terms of labeling, the product name "2,6-difluorobenzene" should be clearly marked on the packaging, and the product parameters, such as molecular weight, boiling point, melting point and other key data, should be listed in detail to clarify its characteristics. And there must be a warning label to indicate its possible risks to ensure the safety of users. Technical specifications should also be strictly adhered to, from the selection of raw materials to the synthesis process, all need to be accurate, so as to obtain high-quality 2,6-difluorobenzene products.
Preparation Method
In order to prepare 2,6-difluorobenzene, the raw materials and the production process, reaction steps and catalytic mechanism are the key.
The raw materials are selected. When selecting a compound containing a benzene ring, and reserving a group that can be substituted by fluorine at a specific position, such as halobenzene, the halogen atom activity should be moderate, which is convenient for subsequent fluorination reactions.
In the production process, the fluorination reaction is the core step. First place the selected raw materials in a suitable reaction vessel and mix the fluorine-containing reagent in proportion. The activity and selectivity of this reagent need to meet the needs of the reaction. Temperature control is in a specific range, and the temperature of different reaction stages is different, or heating or cooling is required to facilitate the forward advancement of the reaction.
The first step is the activation stage. By heating or adding a catalyst, the activity check point of the raw material and the fluorine reagent is activated. The second is the substitution reaction, where the fluorine atom gradually replaces the specific position group. This process requires precise control of the reaction time and the ratio of each substance to avoid side reactions.
Catalytic mechanism, select a high-efficiency catalyst, which may reduce the activation energy of the reaction and accelerate the reaction process. The catalyst or forms an intermediate state with the raw material and reagent to promote the orderly occurrence of the fluorination reaction. After the reaction is completed, the pure 2,6-difluorobenzene product is obtained through separation and purification.
Chemical Reactions & Modifications
It is very important to study the reaction and modification of 2,6-Difluorobenzene in the process of chemical change.
Looking at its reaction, it often involves nucleophilic substitution and the like. Due to the strong electronegativity of fluorine atoms, the electron cloud density of the benzene ring changes, and the adjacent position is affected by it, and the nucleophilic reagent is prone to it. If it encounters a nucleophilic body, or generates a substituted product, the distribution of the electron cloud changes, the direction and rate of the reaction are left and right.
As for modification, different groups can be introduced to adjust its physical and chemical properties. Add specific functional groups, or change their solubility and reactivity. After chemical modification, it may be able to expand its application in the synthesis of materials and drugs.
In summary, further study on the chemical reactions and modifications of 2,6-Difluorobenzene can pave the way for its wider use and better exploration, which is of great significance in various fields of chemistry.
Synonyms & Product Names
The product of 2,6-difluorobenzene is also the product of chemical. Today, its synonyms and trade names are mentioned to clarify its details.
Fu 2,6-difluorobenzene, also known as another name. In the industry, everyone knows this thing. Although there are many synonyms, they all refer to the same quality. Guanfu's trade names also have their own names, but they all represent this 2,6-difluorobenzene product.
Its synonyms are derived from its nature, its construction, or from vulgarity, or according to theory. For the name of the product, the merchant is determined to show the difference of its products and facilitate the sale of the market. Although the names of the two are different, they actually refer to the chemical production of 2,6-difluorobenzene. Those who study this product can obtain its full picture and use it correctly.
Safety & Operational Standards
For 2,6-difluorobenzene, it is also a chemical product. It is related to safety and operating standards, and it is the gist of sincerity and should not be ignored.
All workers must first know its nature when handling this thing. 2,6-difluorobenzene has a special taste and burns. It explodes in the air in case of open flames and high heat energy. During the operation, avoid open flames and hot topics. Workers wear protective clothing, goggles, and anti-poison equipment in front of chemical protection to ensure their own safety.
If this thing is stored, it is advisable to choose a cool and ventilated place, far away from fire and heat sources. The storage temperature should not exceed 37 ° C, and the container should be sealed. Separate storage with oxygen agents and edible chemicals, and mixed transportation is prohibited. When handling, light loading and light unloading, loss-proof container.
If the leakage is on the ground, the source will be cut off immediately, and fire will not be allowed to enter. Emergency responders wear anti-chemical clothing, wear air devices, and leak a small amount. Suction with sand, vermiculite, etc., put a bag to move to a safe place; a large amount of leakage, the embankment is collected, and the tank car is transferred. The residual liquid is pumped to the tank car or special device for disposal.
When handling this product, it complies with safety regulations and follows the rules, so as to ensure the safety of workers and avoid disasters. Everything follows this, so that it is safe and secure.
Application Area
Today there is a thing called 2,6-difluorobenzene, which is quite wonderful in various application fields. In the field of medicine, it can be a key raw material for the creation of new drugs. With its unique chemical properties, it can help doctors develop a cure for the disease and cure the suffering of many diseases.
In the field of materials, it also has extraordinary performance. It can participate in the synthesis of high-tech materials, making the material have different characteristics, or tougher, or more heat-resistant, adding to the long-term durability of utensils.
In the electronics industry, 2,6-difluorobenzene is also indispensable. It can contribute to the manufacturing of electronic components, optimize the performance of components, and make the operation of electronic devices more efficient and stable, thus enabling the industry to thrive and enjoy promising prospects.
Research & Development
In recent years, I have studied a lot of chemical substances, especially 2,6-difluorobenzene. This material is very different and has a wide range of applications. When I first started, its synthesis method was not good, and the yield was not high. I thought about it day and night, consulted classics, and visited Fang's house.
Then I tried various paths, adjusted the conditions of the reaction, and changed the ratio of reagents. After several years, I finally obtained the method of optimization, and the yield was increased. This achievement may be available in the field of industry.
However, I am not satisfied, and I want to dig deeper into its performance and expand its application scope. Ji Neng has opened up new frontiers, enabling 2,6-difluorobenzene to shine in more fields, contributing to the development of chemistry and promoting its continuous progress.
Toxicity Research
Recently, research on 2,6-Difluorobenzene has focused a lot on toxicity research. After various experiments, observe its response to various substances and observe its effect on living beings.
This 2,6-Difluorobenzene has certain toxicity. If you accidentally touch it, the skin may feel uncomfortable, erythema, itching, etc. may appear. If you inhale its gas, you may cause respiratory diseases, cough, asthma, or health.
And in the experiment, try it with small animals. After ingesting this 2,6-Difluorobenzene in moderation, it can be seen that its physiological function has abnormal changes. Its organs may be damaged, and its movement is also slow.
Therefore, when producing and using 2,6-Difluorobenzene, it is necessary to strictly follow the procedures and take comprehensive protection to avoid toxicity and harm, and to ensure the well-being of everyone and the tranquility of the environment.
Future Prospects
The chemical industry is changing with each passing day, and new products are emerging one after another. Today, there is 2,6-difluorobenzene, which is unique in quality and has a wide range of uses. Although it has been used now, the future prospects are still considerable.
Looking at industry, it may be possible to optimize the process, reduce costs and increase efficiency, make the production easier and more abundant. In the field of scientific research, it is expected to open up new avenues, provide materials for various experiments and creations, and explore the unknown. On the medical front, it may also emerge, help the research and development of new drugs, and save patients from pain.
Our chemical researchers should study diligently, with wisdom and sweat, to explore its endless potential, so that 2,6-difluorobenzene will shine in the future and benefit the world.
Where to Buy 2,6-Difluorobenzene in China?
As a trusted 2,6-Difluorobenzene 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.
Frequently Asked Questions

As a leading 2,6-Difluorobenzene 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-difluorobenzene?
2% 2C6-diethylnaphthalene has a wide range of uses. In the field of chemical industry, it is often used as a raw material for the synthesis of various fine chemicals.
First, it can be used to make dyes. The production of dyes is related to people's livelihood, the color of clothes, and the color of fabrics. It depends on this. 2% 2C6-diethylnaphthalene has undergone delicate chemical changes to obtain a dye composition with a special structure. It has good color performance and excellent color fastness, which can make the fabric color gorgeous and lasting.
Second, it is also indispensable in pharmaceutical synthesis. Medical science is related to human life. 2% 2C6-diethylnaphthalene is the basis for building the molecular structure of specific drugs. By means of chemical methods, it is combined with other compounds to make a good medicine for symptoms, so as to cure diseases and relieve the pain of the world.
Furthermore, it has made a name for itself in the field of materials science. Modern technology, based on materials, 2% 2C6-diethylnaphthalene participates in the synthesis of high-performance materials. For example, special polymer materials have excellent physical properties, or high temperature resistance, or corrosion resistance, and are used in many cutting-edge industries such as aerospace and electronic equipment, helping to take off in science and technology.
Because of its special chemical properties, it is an important reagent in the study of organic synthesis reactions. Chemists use it to participate in various reactions, explore reaction mechanisms, expand the boundaries of organic chemistry, and pave the way for the creation of new compounds. All of this shows that 2% 2C6-diethylnaphthalene is of great value in various fields, promoting the progress of industry, medicine, technology and other industries.
What are the physical properties of 2,6-difluorobenzene?
2% 2C6-diethylbenzene is an organic compound with a wide range of uses in the chemical industry. Its physical properties are as follows:
Under normal temperature and pressure, 2% 2C6-diethylbenzene is a colorless and transparent liquid, clear and pure, without visible impurities, similar to the appearance of many common organic solvents.
Smell, has an aromatic smell. This smell is consistent with the characteristic aroma of benzene-based compounds, but its aromatic degree is related to the specific composition ratio.
When it comes to boiling point, it is about 215 ° C - 217 ° C. The boiling point is an important physical constant of the substance, indicating the temperature required for 2% 2C6-diethylbenzene to change from liquid to gaseous state under a specific pressure. This boiling point makes it unique in chemical operations such as distillation and separation.
Its melting point is about -75 ° C, which means that below this temperature, 2% 2C6-diethylbenzene will solidify from a liquid state to a solid state. The melting point is affected by the molecular structure and intermolecular forces, and the molecular structure of 2% 2C6-diethylbenzene determines its melting point value.
In terms of density, it is about 0.867g/cm ³, which is less dense than water. This property causes it to float on the water surface when mixed with water, which needs to be taken into account when liquid-liquid separation operations are involved.
In terms of solubility, 2% 2C6-diethylbenzene is insoluble in water, but can be miscible with most organic solvents such as ethanol, ether, acetone, etc. This solubility is due to the non-polar structure of its molecular structure, which is very different from the polar structure of water, and follows the principle of "similar miscibility".
Is the chemical properties of 2,6-difluorobenzene stable?
Is the chemical properties of 2% 2C6-diethylbenzene stable? This question is related to the importance of chemical industry and cannot be ignored.
The properties of diethylbenzene are stable at room temperature and pressure. It is a colorless liquid with an aromatic taste, insoluble in water, and miscible in organic solvents such as ethanol and ether. This physical property is also characterized by its chemical stability.
However, in special circumstances, its stability is another matter. At high temperatures, diethylbenzene can cause combustion risk, and it is easy to react violently when it encounters with oxidants. This is because there are benzene rings and ethyl groups in its molecular structure. Although benzene rings are conjugated and stable, ethyl groups can be oxidized. Under high temperature, the chemical bond activity is greatly increased, and the stability is reduced.
And diethylbenzene can also react under light or with a catalyst. If under light, the hydrogen atom of the ethyl group can be replaced by a halogen atom, which is a free radical substitution reaction. This example shows that its chemical properties are not absolutely stable, and it can also be active under specific conditions.
In industry, diethylbenzene is often used as a raw material for the production of styrene and is obtained by dehydrogenation. This reaction requires high temperature and a catalyst, which also shows that its chemical properties can be excited under suitable conditions, and it is not blindly stable.
In summary, the chemical properties of 2% 2C6-diethylbenzene are stable under normal conditions. However, in case of high temperature, oxidizing agent, light and specific catalytic conditions, its stability will change or cause reactions to occur. Therefore, its potential activity and danger should not be ignored due to its normal state.
What are the methods for preparing 2,6-difluorobenzene?
The method of making 2% 2C6-diethylnaphthalene has been used in ancient times.
First, the naphthalene is used as the beginning, and the alkylation technique is used. Naphthalene and haloethane, with the help of catalysts, often use aluminum trichloride as the medium, which is suitable for temperature and pressure, and the two are combined. The alkyl group of haloethane is moved over the naphthalene ring. After careful temperature control and timing, the ethyl group can just fall at the 2,6 position to obtain 2,6-diethylnaphthalene. Among them, temperature control is essential, and overheating should be clumped and impure; overcooling should be delayed.
Second, ethylbenzene and phthalic anhydride are used as materials. First, ethylbenzene and phthalic anhydride are made under suitable conditions, and the product containing a specific group is obtained by acylation of Fu-gram. After reduction, dehydration and other delicate changes in multiple steps, it can also reach 2,6-diethylnaphthalene. Each step requires strict selection of reagents and precise control of conditions. For example, in the step of reduction, choose an appropriate reducing agent. The amount and temperature of the product are all related to the quality and quantity of the product.
Third, take 2-ethylnaphthalene as the group, and then alkylate it. In a suitable reaction environment, add an alkylating agent to re-enter the naphthalene ring and select the position to be 2,6-diethylnaphthalene. In this way, it is necessary to make good use of catalysts and reaction aids to adjust the selectivity of the reaction and increase the yield of the target product.
All kinds of production methods have their own advantages and disadvantages. The first raw materials are simple and easy to obtain, but the selectivity may be insufficient; although the secondary steps are complicated, the product structure can be precisely controlled; the three methods are based on specific raw materials and have high requirements for the purity of the raw materials. However, if the raw materials are well prepared, they can be obtained efficiently. For the preparation of 2,6-diethylnaphthalene, it is necessary to choose according to the situation, and to review the ease and difficulty of raw materials, the level of cost, and the demand for products. Only then can the method be determined.
What are the precautions for storing and transporting 2,6-difluorobenzene?
2% 2C6-diethyl ether, when storing and transporting, be sure to pay attention to many matters.
The first thing to pay attention to is its flammability. This is a very flammable material, which is very easy to explode in case of open flames and hot topics. Therefore, the storage place must be away from fire and heat sources, and the ventilation must be good. In the warehouse, electrical installations, lighting, etc. should be explosion-proof, and it is strictly forbidden to use machinery and tools that are prone to sparks. When handling, it should also be handled lightly to prevent damage to packaging and containers, so as not to cause fires.
Second, pay attention to its volatility. Diethyl ether is highly volatile and will form a flammable vapor cloud in the air. Storage containers must be tightly sealed to prevent volatilization from escaping. If in transit, the vehicle should also have good airtightness to prevent leakage.
Third, pay attention to its toxicity. Although the toxicity is relatively not strong, it may still be harmful to the human body if inhaled, ingested or absorbed through the skin. When operating, appropriate protective measures should be taken, such as wearing gas masks, gloves, protective clothing, etc.
Fourth, about storage conditions. It should be stored in a cool and ventilated warehouse, and the storage temperature should not exceed 26 ° C. It should not be mixed with oxidants and other storage and transportation, because it is in contact with oxidants, it is easy to react violently and endanger safety.
Furthermore, when transporting, choose a suitable means of transportation in accordance with relevant regulations, and drive according to the specified route. Transportation vehicles should be equipped with corresponding fire equipment and leakage emergency treatment equipment. Once there is a leak, it can be properly disposed of in time. In this way, the safety of 2% 2C6-diethyl ether during storage and transportation is guaranteed.