Linshang Chemical
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1-(Chloromethyl)-4-(Dichloromethyl)Benzene
Linshang Chemical
|
HS Code |
125594 |
| Chemical Formula | C8H7Cl3 |
| Molecular Weight | 209.5 |
| Appearance | Typically a colorless to pale - yellow liquid |
| Boiling Point | Around 240 - 245 °C |
| Density | Approximately 1.3 - 1.4 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like benzene, toluene |
| Odor | Pungent odor |
| Flash Point | Relatively high, potentially around 100 - 110 °C |
| Vapor Pressure | Low at room temperature |
As an accredited 1-(Chloromethyl)-4-(Dichloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - (Chloromethyl)-4-(dichloromethyl)benzene in 1 - kg bottles, well - sealed for safety. |
| Storage | 1-(Chloromethyl)-4-(dichloromethyl)benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points due to its flammable nature. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials, as it may react with certain substances. Store separately from oxidizing agents, bases, and reactive compounds to prevent unwanted reactions. |
| Shipping | 1-(Chloromethyl)-4-(dichloromethyl)benzene is a chemical. Shipping should be in accordance with hazardous materials regulations. It must be properly packaged to prevent leakage, labeled clearly, and transported by approved carriers. |
Competitive 1-(Chloromethyl)-4-(Dichloromethyl)Benzene 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
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As a leading 1-(Chloromethyl)-4-(Dichloromethyl)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 chemical properties of 1- (chloromethyl) -4- (dichloromethyl) benzene
1- (chloromethyl) -4- (dichloromethyl) benzene, this is an organic compound with unique chemical properties.
It is active in chemical reactions, because it contains chloromethyl and dichloromethyl, chlorine atoms have electron-absorbing properties, resulting in good activity of this digroup. For example, it can react with nucleophiles for nucleophilic substitution. In case of alcohol nucleophiles, chlorine atoms or alkoxy groups are replaced to obtain ether compounds; in case of amine nucleophiles, nitrogen-containing derivatives can be formed.
It is also flammable and reacts with oxygen under specific conditions to produce carbon dioxide, water and hydrogen chloride gas. Pay attention when burning, because its product hydrogen chloride is corrosive and irritating.
In addition, under the action of appropriate catalysts, the benzene ring can participate in some reactions, such as the Fu-g reaction. New groups can be introduced at specific positions of the benzene ring with acyl halides or halogenated hydrocarbons under the catalysis of Lewis acid to expand the derivation path of the compound and obtain new compounds with diverse structures.
When storing and using, in view of its chemical activity and potential danger, strict safety procedures must be followed, properly stored, and protected from contact with incompatible substances to ensure safe operation and avoid accidents.
It is active in chemical reactions, because it contains chloromethyl and dichloromethyl, chlorine atoms have electron-absorbing properties, resulting in good activity of this digroup. For example, it can react with nucleophiles for nucleophilic substitution. In case of alcohol nucleophiles, chlorine atoms or alkoxy groups are replaced to obtain ether compounds; in case of amine nucleophiles, nitrogen-containing derivatives can be formed.
It is also flammable and reacts with oxygen under specific conditions to produce carbon dioxide, water and hydrogen chloride gas. Pay attention when burning, because its product hydrogen chloride is corrosive and irritating.
In addition, under the action of appropriate catalysts, the benzene ring can participate in some reactions, such as the Fu-g reaction. New groups can be introduced at specific positions of the benzene ring with acyl halides or halogenated hydrocarbons under the catalysis of Lewis acid to expand the derivation path of the compound and obtain new compounds with diverse structures.
When storing and using, in view of its chemical activity and potential danger, strict safety procedures must be followed, properly stored, and protected from contact with incompatible substances to ensure safe operation and avoid accidents.
What are the main uses of 1- (chloromethyl) -4- (dichloromethyl) benzene
1- (chloromethyl) -4- (dichloromethyl) benzene, which has a wide range of uses. In the field of organic synthesis, it is a key raw material and can be used to produce a variety of organic compounds with unique functions. For example, through specific chemical reactions, it can be converted into complex aromatic hydrocarbon derivatives containing chlorine. In the field of pharmaceutical research and development, such derivatives may have unique biological activities and can be used as potential drug intermediates, laying the foundation for the creation of new drugs.
Furthermore, in the field of materials science, 1- (chloromethyl) -4- (dichloromethyl) benzene also has wonderful uses. After appropriate polymerization, it can participate in the preparation of special polymer materials. Such materials may have excellent chemical stability, heat resistance and other properties, and are very useful in high-end fields such as aerospace, electronics and electrical appliances. For example, they are used in the manufacture of spacecraft parts and can withstand harsh environments. They are used as insulating materials for electronic appliances to ensure the stable operation of equipment.
In addition, in the fine chemical industry, they can be used as a starting material for the synthesis of special fragrances and dyes. Through the delicate chemical synthesis path, the fragrances are endowed with a unique aroma, adding a bright color and excellent fastness to the dyes, and satisfying people's pursuit of high-quality life and product appearance. In short, 1- (chloromethyl) -4- (dichloromethyl) benzene plays an important role in many fields and is of great significance to promote the development of various industries.
Furthermore, in the field of materials science, 1- (chloromethyl) -4- (dichloromethyl) benzene also has wonderful uses. After appropriate polymerization, it can participate in the preparation of special polymer materials. Such materials may have excellent chemical stability, heat resistance and other properties, and are very useful in high-end fields such as aerospace, electronics and electrical appliances. For example, they are used in the manufacture of spacecraft parts and can withstand harsh environments. They are used as insulating materials for electronic appliances to ensure the stable operation of equipment.
In addition, in the fine chemical industry, they can be used as a starting material for the synthesis of special fragrances and dyes. Through the delicate chemical synthesis path, the fragrances are endowed with a unique aroma, adding a bright color and excellent fastness to the dyes, and satisfying people's pursuit of high-quality life and product appearance. In short, 1- (chloromethyl) -4- (dichloromethyl) benzene plays an important role in many fields and is of great significance to promote the development of various industries.
What are the synthesis methods of 1- (chloromethyl) -4- (dichloromethyl) benzene
1 - (chloromethyl) -4- (dichloromethyl) benzene is also an organic compound. There are several ways to synthesize it.
One method can start from p-xylene. p-xylene uses chlorine as a halogenating agent, and under the condition of light or heating, the methyl group can be chlorinated. At first, one hydrogen atom on the methyl group is replaced by a chlorine atom to obtain 4-methyl benzyl chloride. Continued, in a suitable reaction environment, this product interacts with chlorine gas to gradually chlorinate another methyl group, first obtaining 1 - (chloromethyl) -4- (chloromethyl) benzene, and then obtaining 1 - (chloromethyl) -4- (dichloromethyl) benzene. In this process, under the conditions of light or heating, the chlorine gas molecules can be homogenized into chlorine radicals, triggering free radical substitution reactions.
Another method, or you can start with p-chlorotoluene. After chloromethylation of p-chlorotoluene, polyformaldehyde, hydrogen chloride and zinc salts are used as reagents. At an appropriate temperature and reaction time, the methyl groups on the benzene ring can be introduced into the chloromethyl group to generate 1- (chloromethyl) -4- (chloromethyl) benzene, and then further chlorinated to obtain the target product 1- (chloromethyl) -4- (dichloromethyl) benzene. This chloromethylation reaction realizes the chloromethylation of the benzene ring side chain methyl through the interaction between reagents.
In another method, suitable organometallic reagents can be considered to react with chlorine-containing aromatic hydrocarbon derivatives. For example, a certain organolithium reagent or Grignard reagent is used with a specific halogenated aromatic hydrocarbon. Under strict reaction conditions such as anhydrous and anaerobic, through a series of nucleophilic substitution or addition-elimination reaction steps, the structure of the target molecule is gradually constructed, and finally 1- (chloromethyl) -4- (dichloromethyl) benzene is synthesized. However, this method requires strict reaction conditions and fine operation to ensure the smooth progress of the reaction and the purity of the product.
One method can start from p-xylene. p-xylene uses chlorine as a halogenating agent, and under the condition of light or heating, the methyl group can be chlorinated. At first, one hydrogen atom on the methyl group is replaced by a chlorine atom to obtain 4-methyl benzyl chloride. Continued, in a suitable reaction environment, this product interacts with chlorine gas to gradually chlorinate another methyl group, first obtaining 1 - (chloromethyl) -4- (chloromethyl) benzene, and then obtaining 1 - (chloromethyl) -4- (dichloromethyl) benzene. In this process, under the conditions of light or heating, the chlorine gas molecules can be homogenized into chlorine radicals, triggering free radical substitution reactions.
Another method, or you can start with p-chlorotoluene. After chloromethylation of p-chlorotoluene, polyformaldehyde, hydrogen chloride and zinc salts are used as reagents. At an appropriate temperature and reaction time, the methyl groups on the benzene ring can be introduced into the chloromethyl group to generate 1- (chloromethyl) -4- (chloromethyl) benzene, and then further chlorinated to obtain the target product 1- (chloromethyl) -4- (dichloromethyl) benzene. This chloromethylation reaction realizes the chloromethylation of the benzene ring side chain methyl through the interaction between reagents.
In another method, suitable organometallic reagents can be considered to react with chlorine-containing aromatic hydrocarbon derivatives. For example, a certain organolithium reagent or Grignard reagent is used with a specific halogenated aromatic hydrocarbon. Under strict reaction conditions such as anhydrous and anaerobic, through a series of nucleophilic substitution or addition-elimination reaction steps, the structure of the target molecule is gradually constructed, and finally 1- (chloromethyl) -4- (dichloromethyl) benzene is synthesized. However, this method requires strict reaction conditions and fine operation to ensure the smooth progress of the reaction and the purity of the product.
1- (chloromethyl) -4- (dichloromethyl) benzene during storage and transportation
1 - (chloromethyl) - 4 - (dichloromethyl) benzene is also an organic compound. When storing and transporting, be sure to pay attention to many matters.
The first to bear the brunt is related to storage. Because of its certain chemical activity, it should be placed in a cool, dry and well-ventilated place. This is to avoid chemical changes caused by moisture or heat, causing danger. Cover a humid environment, or cause reactions such as hydrolysis; hot topic, or promote its decomposition, volatilization, and even the risk of combustion and explosion. And need to be separated from oxidants, strong bases and other substances. Both the edge oxidizer and the strong alkali can react violently with 1- (chloromethyl) -4- (dichloromethyl) benzene, causing accidental disasters.
Furthermore, when transporting, do not slack off. The container containing this thing must be well sealed and durable. To prevent the container from being damaged due to bumps and collisions during transportation, resulting in leakage of 1- (chloromethyl) -4- (dichloromethyl) benzene. If it leaks outside, it will not only pollute the environment, but also endanger the safety of humans and animals. Transportation vehicles should also be equipped with corresponding emergency treatment equipment, such as adsorption materials, fire extinguishers, etc. In case of leakage, it can be disposed of in time. And transport personnel must undergo professional training, familiar with the characteristics of 1 - (chloromethyl) - 4 - (dichloromethyl) benzene and emergency treatment methods, so as to ensure the smooth storage and transportation and avoid disasters.
The first to bear the brunt is related to storage. Because of its certain chemical activity, it should be placed in a cool, dry and well-ventilated place. This is to avoid chemical changes caused by moisture or heat, causing danger. Cover a humid environment, or cause reactions such as hydrolysis; hot topic, or promote its decomposition, volatilization, and even the risk of combustion and explosion. And need to be separated from oxidants, strong bases and other substances. Both the edge oxidizer and the strong alkali can react violently with 1- (chloromethyl) -4- (dichloromethyl) benzene, causing accidental disasters.
Furthermore, when transporting, do not slack off. The container containing this thing must be well sealed and durable. To prevent the container from being damaged due to bumps and collisions during transportation, resulting in leakage of 1- (chloromethyl) -4- (dichloromethyl) benzene. If it leaks outside, it will not only pollute the environment, but also endanger the safety of humans and animals. Transportation vehicles should also be equipped with corresponding emergency treatment equipment, such as adsorption materials, fire extinguishers, etc. In case of leakage, it can be disposed of in time. And transport personnel must undergo professional training, familiar with the characteristics of 1 - (chloromethyl) - 4 - (dichloromethyl) benzene and emergency treatment methods, so as to ensure the smooth storage and transportation and avoid disasters.
What are the effects of 1- (chloromethyl) -4- (dichloromethyl) benzene on the environment and human health?
1- (chloromethyl) -4- (dichloromethyl) benzene, this substance has many effects on the environment and human health.
At the environmental level, it has a certain degree of volatility, which is emitted into the atmosphere, and may affect the air quality, thereby harming surrounding organisms. And because of its chemical properties, it may remain and accumulate in soil and water bodies, interfering with the balance of ecosystems. If it enters the water body, it may be toxic to aquatic organisms, damage the aquatic ecological environment, change the population structure of aquatic organisms, and hinder the self-purification ability of the water body.
It is related to human health, and this substance may be irritating. Inhaled through the respiratory tract, it will irritate the respiratory mucosa, causing symptoms such as cough, asthma, breathing difficulties, and long-term exposure or respiratory diseases. Through skin contact, it may irritate the skin, causing skin redness, itching, allergies and other conditions. If ingested inadvertently, it may cause damage to the digestive system, resulting in nausea, vomiting, abdominal pain and other symptoms. What needs to be more vigilant is that some compounds containing such structures may be potentially carcinogenic, long-term exposure may increase the risk of cancer.
Therefore, when producing, using and handling products containing 1- (chloromethyl) -4- (dichloromethyl) benzene, proper protective measures must be taken to reduce the harm to the environment and human body.
At the environmental level, it has a certain degree of volatility, which is emitted into the atmosphere, and may affect the air quality, thereby harming surrounding organisms. And because of its chemical properties, it may remain and accumulate in soil and water bodies, interfering with the balance of ecosystems. If it enters the water body, it may be toxic to aquatic organisms, damage the aquatic ecological environment, change the population structure of aquatic organisms, and hinder the self-purification ability of the water body.
It is related to human health, and this substance may be irritating. Inhaled through the respiratory tract, it will irritate the respiratory mucosa, causing symptoms such as cough, asthma, breathing difficulties, and long-term exposure or respiratory diseases. Through skin contact, it may irritate the skin, causing skin redness, itching, allergies and other conditions. If ingested inadvertently, it may cause damage to the digestive system, resulting in nausea, vomiting, abdominal pain and other symptoms. What needs to be more vigilant is that some compounds containing such structures may be potentially carcinogenic, long-term exposure may increase the risk of cancer.
Therefore, when producing, using and handling products containing 1- (chloromethyl) -4- (dichloromethyl) benzene, proper protective measures must be taken to reduce the harm to the environment and human body.
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