Linshang Chemical
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3,5-Dinitro-4-Chloro Trifluoromethylbenzene
Linshang Chemical
|
HS Code |
324243 |
| Chemical Formula | C7H2ClF3N2O4 |
| Molecular Weight | 272.55 |
| Appearance | Typically a solid |
| Color | May be yellowish |
| Melting Point | Specific value would require further research |
| Boiling Point | Specific value would require further research |
| Solubility In Water | Low solubility in water |
| Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane |
| Density | Specific value would require further research |
| Stability | Stable under normal conditions, but may react with strong oxidizing agents |
As an accredited 3,5-Dinitro-4-Chloro Trifluoromethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 3,5 - dinitro - 4 - chloro Trifluoromethylbenzene in sealed chemical - grade packaging. |
| Storage | 3,5 - dinitro - 4 - chloro trifluoromethylbenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, ignition sources, and incompatible substances. Store in a tightly - sealed container, preferably in a corrosion - resistant material, to prevent leakage and exposure. Classify it according to its hazardous nature and ensure proper labeling for safety. |
| Shipping | 3,5 - dinitro - 4 - chloro trifluoromethylbenzene is a chemical. Shipments must comply with strict regulations. It should be properly packaged in corrosion - resistant containers, labeled clearly, and transported by carriers authorized for hazardous chemicals. |
Competitive 3,5-Dinitro-4-Chloro Trifluoromethylbenzene 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.
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Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 3,5-Dinitro-4-Chloro Trifluoromethylbenzene in China?
As a trusted 3,5-Dinitro-4-Chloro Trifluoromethylbenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
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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 3,5-Dinitro-4-Chloro Trifluoromethylbenzene 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 3,5-dinitro-4-chlorotrifluoromethylbenzene?
3,5-Dichloro-4-fluorotrifluoromethylbenzene, which has a wide range of uses. In the field of medicine, it is a key intermediate and can help synthesize many specific drugs. For example, when developing targeted drugs for specific diseases, its unique chemical structure can precisely target diseased cells, improve drug efficacy, and reduce damage to normal cells, bringing good news to patients.
In the field of pesticides, it is also an important raw material. The pesticides produced have the characteristics of high efficiency, low toxicity, and broad spectrum, which can effectively kill various pests and ensure the growth of crops. For common pests such as aphids and mites, pesticides made from this raw material can quickly inhibit their reproduction, reduce the damage of pests to crops, improve crop yield and quality, and protect agricultural harvests.
In the field of materials science, 3,5-dichloro-4-fluorotrifluoromethylbenzene also plays an important role. It can be used to prepare high-performance special materials with excellent chemical stability, heat resistance and mechanical properties. For example, it can meet the needs of aircraft in extreme environments and ensure the safe and stable operation of aircraft. In the manufacture of electronic equipment, it can improve the performance and reliability of electronic components and help electronic products to be continuously upgraded.
In the field of pesticides, it is also an important raw material. The pesticides produced have the characteristics of high efficiency, low toxicity, and broad spectrum, which can effectively kill various pests and ensure the growth of crops. For common pests such as aphids and mites, pesticides made from this raw material can quickly inhibit their reproduction, reduce the damage of pests to crops, improve crop yield and quality, and protect agricultural harvests.
In the field of materials science, 3,5-dichloro-4-fluorotrifluoromethylbenzene also plays an important role. It can be used to prepare high-performance special materials with excellent chemical stability, heat resistance and mechanical properties. For example, it can meet the needs of aircraft in extreme environments and ensure the safe and stable operation of aircraft. In the manufacture of electronic equipment, it can improve the performance and reliability of electronic components and help electronic products to be continuously upgraded.
What are the physical properties of 3,5-dinitro-4-chlorotrifluoromethylbenzene?
3,5-Dihydroxy-4-methoxytrifluoromethylbenzene, this substance is an organic compound with specific physical and chemical properties. Its physical properties are as follows:
Viewed, it is often white to light yellow crystalline powder, which is conducive to observation and resolution. In many experiments and production scenarios, its state and purity can be preliminarily determined by its appearance.
Smell, no significant odor, this characteristic makes it free from pungent or special odor interference during operation and application, avoid discomfort caused by odor, and add convenience to the use process.
Melting, the melting point is in a specific range, generally in [X] ℃ - [X] ℃, the melting point is an important physical constant of the substance, which is of great significance for its identification and purity judgment. The precise melting point indicates that the compound is structurally stable and has high purity; if the melting point is abnormal, or it suggests that there are impurities mixed in.
It dissolves, and its solubility varies in organic solvents. In common organic solvents such as ethanol and acetone, it has certain solubility and can form a uniform solution. This solubility is convenient for chemical synthesis, drug preparation and other fields as reactants or intermediates, with suitable solvents to help it participate in the reaction. However, its solubility in water is poor, because its molecular structure contains hydrophobic groups, resulting in poor hydrophilicity.
In addition, the density of the compound is about [X] g/cm ³, and the density reflects the compactness of the substance, which has a great impact on storage, transportation and related process design. Knowing the density, the storage container and transportation method can be reasonably planned to ensure safety and efficiency.
In summary, the physical properties of 3,5-dihydroxy-4-methoxytrifluoromethylbenzene lay the foundation for its application in scientific research, production and other fields, and are essential for in-depth understanding and rational use of this compound.
Viewed, it is often white to light yellow crystalline powder, which is conducive to observation and resolution. In many experiments and production scenarios, its state and purity can be preliminarily determined by its appearance.
Smell, no significant odor, this characteristic makes it free from pungent or special odor interference during operation and application, avoid discomfort caused by odor, and add convenience to the use process.
Melting, the melting point is in a specific range, generally in [X] ℃ - [X] ℃, the melting point is an important physical constant of the substance, which is of great significance for its identification and purity judgment. The precise melting point indicates that the compound is structurally stable and has high purity; if the melting point is abnormal, or it suggests that there are impurities mixed in.
It dissolves, and its solubility varies in organic solvents. In common organic solvents such as ethanol and acetone, it has certain solubility and can form a uniform solution. This solubility is convenient for chemical synthesis, drug preparation and other fields as reactants or intermediates, with suitable solvents to help it participate in the reaction. However, its solubility in water is poor, because its molecular structure contains hydrophobic groups, resulting in poor hydrophilicity.
In addition, the density of the compound is about [X] g/cm ³, and the density reflects the compactness of the substance, which has a great impact on storage, transportation and related process design. Knowing the density, the storage container and transportation method can be reasonably planned to ensure safety and efficiency.
In summary, the physical properties of 3,5-dihydroxy-4-methoxytrifluoromethylbenzene lay the foundation for its application in scientific research, production and other fields, and are essential for in-depth understanding and rational use of this compound.
What are the chemical properties of 3,5-dinitro-4-chlorotrifluoromethylbenzene?
3,5-Dichloro-4-fluorotrifluoromethylbenzene is an organic compound with unique chemical properties and is widely used in many fields of chemical industry. The following is described in detail according to the classical Chinese style of "Tiangong Kaiwu".
This compound has the properties of halogenated aromatics. The introduction of halogen atoms such as fluorine and chlorine makes it highly chemically stable. Due to the strong electronegativity of fluorine atoms, after connecting with the benzene ring, the electron cloud density distribution of the benzene ring changes, and the electrophilic substitution reaction activity is reduced compared with that of benzene. Chlorine atoms also affect the electron cloud of the benzene ring, and cooperate with fluorine atoms, making it difficult for the compound to react with common reagents under normal conditions.
In the nucleophilic substitution reaction, although the electron cloud density of 3,5-dichloro-4-fluorotrifluoromethylbenzene decreases, the halogen atom can be used as the leaving group. Under appropriate nucleophilic reagents and reaction conditions, the halogen atom can be replaced by a nucleophilic reagent. For example, with sodium alcohol as the nucleophilic reagent, in a heating and appropriate solvent environment, the halogen atom can be replaced by an alkoxy group to generate the corresponding alkoxy-containing derivative.
It also has certain oxidizing and reducing properties. Under the action of strong oxidants, the benzene ring may be oxidized to form compounds containing functional groups such as carboxyl groups. In the case of strong reducing agents, the halogen atom may be reduced and removed and converted into benzene derivatives.
3,5-dichloro-4-fluorotrifluoromethylbenzene has unique chemical properties. The interaction between halogen atoms and benzene rings makes it an important intermediate in the field of organic synthesis. It can be prepared through various reaction pathways. A variety of organic compounds with special properties play a key role in the creation of fine chemical products, medicine, and pesticides.
This compound has the properties of halogenated aromatics. The introduction of halogen atoms such as fluorine and chlorine makes it highly chemically stable. Due to the strong electronegativity of fluorine atoms, after connecting with the benzene ring, the electron cloud density distribution of the benzene ring changes, and the electrophilic substitution reaction activity is reduced compared with that of benzene. Chlorine atoms also affect the electron cloud of the benzene ring, and cooperate with fluorine atoms, making it difficult for the compound to react with common reagents under normal conditions.
In the nucleophilic substitution reaction, although the electron cloud density of 3,5-dichloro-4-fluorotrifluoromethylbenzene decreases, the halogen atom can be used as the leaving group. Under appropriate nucleophilic reagents and reaction conditions, the halogen atom can be replaced by a nucleophilic reagent. For example, with sodium alcohol as the nucleophilic reagent, in a heating and appropriate solvent environment, the halogen atom can be replaced by an alkoxy group to generate the corresponding alkoxy-containing derivative.
It also has certain oxidizing and reducing properties. Under the action of strong oxidants, the benzene ring may be oxidized to form compounds containing functional groups such as carboxyl groups. In the case of strong reducing agents, the halogen atom may be reduced and removed and converted into benzene derivatives.
3,5-dichloro-4-fluorotrifluoromethylbenzene has unique chemical properties. The interaction between halogen atoms and benzene rings makes it an important intermediate in the field of organic synthesis. It can be prepared through various reaction pathways. A variety of organic compounds with special properties play a key role in the creation of fine chemical products, medicine, and pesticides.
What is the production method of 3,5-dinitro-4-chlorotrifluoromethylbenzene?
The preparation of 3,5-dihydroxy-4-chlorotrifluoromethylbenzene is a very important chemical process. The preparation method usually follows the following steps:
First, a suitable starting material is selected, and a benzene compound with a specific substituent is selected. This starting material must have the structural characteristics of the desired group that can be converted into the target product by chemical reaction.
One method can first halogenate the benzene ring. Select a suitable halogenating agent, such as a chlorine-containing halogenating agent, and under specific reaction conditions, the chlorine atom is precisely introduced into the benzene ring at a specific position. This reaction condition is very critical, such as reaction temperature, reaction time and reaction solvent, which need to be carefully regulated. If the temperature is too high or too low, the halogenation position may be selectively shifted, or the reaction rate may be too slow, and side reactions may increase. Generally speaking, the reaction temperature may be controlled in a specific range, such as tens of degrees Celsius, and the chlorination at a specific position of the benzene ring can be achieved after a certain period of time.
Then, the hydroxylation reaction is carried out. This step aims to introduce dihydroxy groups. It is often reacted with halogenated benzene ring compounds with the help of specific hydroxylating reagents. This reaction may need to be carried out in an alkaline environment to promote the substitution of hydroxyl groups on the benzene ring. During the reaction, factors such as the strength of basicity and the proportion of reagents used have a great impact on the effect of hydroxylation. It takes many tests to find the best reaction parameters before the hydroxyl group can be successfully and accurately introduced into the 3,5-position to form a 3,5-dihydroxyl structure.
After the hydroxyl group is introduced, trifluoromethyl is introduced. This process usually uses reagents containing trifluoromethyl, and through a specific organic reaction mechanism, trifluoromethyl is connected to the benzene ring. This reaction step may involve the use of catalysts to improve the reaction efficiency and selectivity. The type, dosage and control of reaction conditions, such as temperature and pressure, have a significant impact on the yield and purity of the final product.
After the above series of reaction steps, followed by separation, purification and other post-processing steps, the impurities and by-products generated during the reaction are removed, and the high-purity 3,5-dihydroxy-4-chlorotrifluoromethylbenzene is finally obtained. Although this preparation method is complicated, each step of the reaction has been repeatedly explored and optimized by many chemical researchers, which is an effective preparation method at present.
First, a suitable starting material is selected, and a benzene compound with a specific substituent is selected. This starting material must have the structural characteristics of the desired group that can be converted into the target product by chemical reaction.
One method can first halogenate the benzene ring. Select a suitable halogenating agent, such as a chlorine-containing halogenating agent, and under specific reaction conditions, the chlorine atom is precisely introduced into the benzene ring at a specific position. This reaction condition is very critical, such as reaction temperature, reaction time and reaction solvent, which need to be carefully regulated. If the temperature is too high or too low, the halogenation position may be selectively shifted, or the reaction rate may be too slow, and side reactions may increase. Generally speaking, the reaction temperature may be controlled in a specific range, such as tens of degrees Celsius, and the chlorination at a specific position of the benzene ring can be achieved after a certain period of time.
Then, the hydroxylation reaction is carried out. This step aims to introduce dihydroxy groups. It is often reacted with halogenated benzene ring compounds with the help of specific hydroxylating reagents. This reaction may need to be carried out in an alkaline environment to promote the substitution of hydroxyl groups on the benzene ring. During the reaction, factors such as the strength of basicity and the proportion of reagents used have a great impact on the effect of hydroxylation. It takes many tests to find the best reaction parameters before the hydroxyl group can be successfully and accurately introduced into the 3,5-position to form a 3,5-dihydroxyl structure.
After the hydroxyl group is introduced, trifluoromethyl is introduced. This process usually uses reagents containing trifluoromethyl, and through a specific organic reaction mechanism, trifluoromethyl is connected to the benzene ring. This reaction step may involve the use of catalysts to improve the reaction efficiency and selectivity. The type, dosage and control of reaction conditions, such as temperature and pressure, have a significant impact on the yield and purity of the final product.
After the above series of reaction steps, followed by separation, purification and other post-processing steps, the impurities and by-products generated during the reaction are removed, and the high-purity 3,5-dihydroxy-4-chlorotrifluoromethylbenzene is finally obtained. Although this preparation method is complicated, each step of the reaction has been repeatedly explored and optimized by many chemical researchers, which is an effective preparation method at present.
What are the precautions for using 3,5-dinitro-4-chlorotrifluoromethylbenzene?
3,5-Dichloro-4-fluorotrifluoromethylbenzene is a special chemical. When using it, there are many key precautions to be paid attention to.
Those who bear the brunt should not be ignored for safety protection. This substance is toxic and irritating to a certain extent. When coming into contact, be sure to wear complete protective equipment, such as protective clothing, protective gloves and protective goggles, to prevent it from coming into contact with the skin and eyes. If you accidentally touch it, you should immediately rinse it with plenty of water and decide whether to seek medical attention according to the severity of the injury.
Furthermore, caution should be taken when storing. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. At the same time, it should be stored separately from oxidizing agents, acids, alkalis and other substances to prevent dangerous chemical reactions.
During use, ventilation of the operating environment is essential. It must be operated in a place with effective ventilation equipment to avoid the accumulation of volatile gaseous substances in the air, which may endanger the health of the operator.
Moreover, accurate dosage control is indispensable. According to specific experimental or production requirements, accurately weigh the required amount. Do not increase or decrease it at will, so as not to affect the experimental results or production quality, and even cause safety accidents.
In addition, after use, the remaining substances and waste should not be discarded at will. It is necessary to properly handle it in accordance with relevant regulations to prevent pollution to the environment.
In short, when using 3,5-dichloro-4-fluorotrifluoromethylbenzene, it is necessary to strictly follow the safety operating procedures and do a good job in all protection and management to ensure the safety of personnel and the environment.
Those who bear the brunt should not be ignored for safety protection. This substance is toxic and irritating to a certain extent. When coming into contact, be sure to wear complete protective equipment, such as protective clothing, protective gloves and protective goggles, to prevent it from coming into contact with the skin and eyes. If you accidentally touch it, you should immediately rinse it with plenty of water and decide whether to seek medical attention according to the severity of the injury.
Furthermore, caution should be taken when storing. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. At the same time, it should be stored separately from oxidizing agents, acids, alkalis and other substances to prevent dangerous chemical reactions.
During use, ventilation of the operating environment is essential. It must be operated in a place with effective ventilation equipment to avoid the accumulation of volatile gaseous substances in the air, which may endanger the health of the operator.
Moreover, accurate dosage control is indispensable. According to specific experimental or production requirements, accurately weigh the required amount. Do not increase or decrease it at will, so as not to affect the experimental results or production quality, and even cause safety accidents.
In addition, after use, the remaining substances and waste should not be discarded at will. It is necessary to properly handle it in accordance with relevant regulations to prevent pollution to the environment.
In short, when using 3,5-dichloro-4-fluorotrifluoromethylbenzene, it is necessary to strictly follow the safety operating procedures and do a good job in all protection and management to ensure the safety of personnel and the environment.
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