1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene

Linshang Chemical

Specifications

HS Code

870647

Chemical Formula C8H2Cl2F6
Molecular Weight 289.00
Appearance colorless to light yellow liquid
Boiling Point 164 - 166 °C
Density 1.598 g/cm³
Solubility Insoluble in water, soluble in organic solvents
Flash Point 63 °C
Stability Stable under normal conditions

As an accredited 1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 500g of 1,4 - dichloro - 2,5 - bis(trifluoromethyl)benzene packaged in air - tight glass bottles.
Storage 1,4 - Dichloro - 2,5 - bis(trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly closed container, preferably made of corrosion - resistant materials. This is to prevent evaporation, potential reactions, and ensure safety due to its chemical properties.
Shipping 1,4 - dichloro - 2,5 - bis(trifluoromethyl)benzene is shipped in tightly sealed, corrosion - resistant containers. Special care is taken to comply with hazardous chemical shipping regulations, ensuring safe transport.
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1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene 1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene
General Information
Where to Buy 1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene in China?
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Frequently Asked Questions

As a leading 1,4-Dichloro-2,5-Bis(Trifluoromethyl)Benzene 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 1,4-dichloro-2,5-bis (trifluoromethyl) benzene?
1% 2C4-dioxy-2% 2C5-bis (triethoxy) benzene is one of the organic compounds. It has a wide range of uses and is often used as a raw material for organic synthesis in the chemical industry.
In materials science, this compound can participate in the preparation of polymer materials. By combining with other monomers through specific chemical reactions, it can affect the structure and properties of polymer materials. Its unique chemical structure endows the material with specific properties, such as enhancing the stability of the material and improving its mechanical properties.
In the field of medicinal chemistry, it also has potential application value. Due to its structural characteristics, it may be used as a drug intermediate to provide a basis for the synthesis of new drugs. After chemical modification and modification, it is expected to develop drugs with specific pharmacological activities to deal with various diseases.
In the field of electronics, it may be used to make electronic materials. With its own electrical properties and chemical stability, it plays a role in the manufacture of electronic components, such as participating in the preparation of printed circuit board materials, affecting the performance of circuit boards, improving their electrical insulation, thermal stability, etc.
Due to its special structure, this compound has shown important uses in many fields such as chemical industry, materials, medicine, electronics, etc. With the continuous progress of science and technology, its application prospects may be broader.
What are the physical properties of 1,4-dichloro-2,5-bis (trifluoromethyl) benzene?
1% 2C4-dioxy-2% 2C5-bis (triethoxy) benzene. The physical properties of this substance are as follows:
It is an organic compound. It is colorless to light yellow at room temperature and has a certain volatility. Due to the specific functional group structure, the intermolecular force is in a specific situation, which determines the melting and boiling point of the substance. Its melting point is low, and it can maintain a liquid state at room temperature. The boiling point may be in a certain temperature range. The specific value varies due to factors such as purity.
The density of this substance is less than that of water. If mixed with water, it will float on the water surface. Insoluble in water, because it is an organic molecule, it is hydrophobic, and hydrogen bonds are formed between water molecules, causing the two to be insoluble. However, it is soluble in common organic solvents, such as ethanol, ether, chloroform, etc., because it follows the principle of similarity dissolution, that is, substances with similar structures are easy to dissolve with each other.
It also has a certain refractive index. When light passes through the substance, the propagation direction will change according to specific laws. This property can be used in the field of material purity detection. And in the electric field, magnetic field environment, or due to the distribution of charge in molecules, it presents specific electrical and magnetic properties, but the relevant specific performance needs to be accurately determined according to its microstructure and external field strength.
What are the chemical properties of 1,4-dichloro-2,5-bis (trifluoromethyl) benzene?
1% 2C4-dioxy-2% 2C5-bis (triethoxy) benzene, this substance is a member of the field of organic compounds. Its chemical properties contain many interesting aspects.
Looking at its structure, oxygen atoms are connected to the benzene ring, forming a unique chemical environment. This gives the substance a specific electron cloud distribution. The dioxy structure makes the molecule have a certain polarity, which has a significant impact on its physical and chemical properties. The existence of polarity makes the solubility of the substance in solvents biased towards polar solvents.
Looking at the bi (triethoxy) part again, the triethoxy group has a relatively large steric barrier. This steric barrier affects the interaction between molecules. In chemical reactions, the steric hindrance effect can change the reaction path and rate. For example, in nucleophilic substitution reactions, large steric hindrances may prevent nucleophiles from approaching the reaction center, thereby reducing the reaction rate.
In terms of stability, the conjugated structure of the benzene ring provides a certain degree of stability for the molecule. However, the oxygen-oxygen bond in the dioxy structure is relatively weak. Under certain conditions, such as heat, light or the presence of suitable initiators, this oxygen-oxygen bond may break, initiating a series of chemical reactions.
In the field of organic synthesis, 1% 2C4-dioxy-2% 2C5-bis (triethoxy) benzene can be used as an important intermediate. Due to its unique chemical properties, it can participate in a variety of reactions and build more complex organic molecular structures, providing a powerful tool for the development of organic synthetic chemistry.
What is the production method of 1,4-dichloro-2,5-bis (trifluoromethyl) benzene?
The preparation method of 1% 2C4-dioxy-2% 2C5-bis (triethoxysilyl) benzene is as follows:
First, an appropriate amount of raw material is taken, which contains the starting material that can be used to construct the basic framework of the compound. Usually, compounds with suitable functional groups need to be carefully selected, such as reagents containing silicon groups with reactive check points, and raw materials that can combine with silicon-based reagents to form the target benzene ring structure.
In a clean and dry reaction vessel, the selected raw materials are mixed in precise proportions. The proportions need to be repeatedly adjusted according to the stoichiometric relationship of the chemical reaction and the actual reaction effect to achieve the best reaction yield.
Then, a suitable catalyst is added. The choice of catalyst is crucial, which can significantly affect the reaction rate and selectivity. Under specific reaction conditions, catalysts that can promote the partial bonding of silica and benzene rings, such as certain metal salts or organic bases, can be selected.
Set the appropriate reaction temperature and time. The reaction temperature needs to be precisely controlled, neither too high to cause frequent side reactions, nor too low to slow down the reaction rate. Generally speaking, this reaction may be carried out within a certain temperature range and last for several hours, depending on the monitoring of the reaction process. During the reaction process, the changes in the reaction system are closely observed, and the reaction process can be tracked by means such as thin-layer chromatography to determine whether the reaction has reached the expected degree.
After the reaction is completed, a suitable separation and purification method can be used. Insoluble impurities and reaction by-products can be removed by initial operations such as filtration and extraction. Then, fine separation techniques such as column chromatography are used to further purify the product to obtain high-purity 1% 2C4-dioxy-2% 2C5-bis (triethoxysilyl) benzene. In this way, after a series of rigorous operations, the target product can be obtained.
What are the precautions for using 1,4-dichloro-2,5-bis (trifluoromethyl) benzene?
1% 2C4-dioxy-2% 2C5-bis (triethoxy) benzene. When using this substance, many matters need to be paid attention to.
First, it has a certain chemical activity, and when mixing with other substances, be cautious. It is necessary to check whether there is any potential chemical reaction between it and the various chemical substances it comes into contact with, in order to prevent sudden violent reactions, resulting in danger, such as explosion, fire or the formation of harmful substances.
Furthermore, its physical properties should not be ignored. The melting point, boiling point, solubility and other properties of this substance will affect its storage and use. When storing, according to its characteristics, choose the appropriate temperature and humidity environment to ensure its stability and avoid deterioration due to environmental factors.
And this thing may pose a certain hazard to the human body. During operation, complete protective measures must be taken. Wear appropriate protective equipment, such as protective gloves, goggles, masks, etc., to prevent it from touching the skin, eyes, or being inhaled into the body. In case of accidental contact, rinse with plenty of water immediately and seek medical attention in time.
In addition, in the site of use, ventilation conditions must be good. This can effectively reduce the concentration of this thing in the air after evaporation, reduce the risk of human inhalation, and avoid the formation of an explosive gas environment.
Accurate measurement is also crucial when taking it. When taking it strictly according to the amount required for experiment or production, do not increase or decrease it at will, so as not to affect the experimental results or production process. After use, properly dispose of the residue, do not discard it at will, and deal with it harmlessly in accordance with relevant regulations to prevent pollution to the environment.