Linshang Chemical
PRODUCTS
1-Chloro-3-(Methylsulfanyl)Benzene
Linshang Chemical
|
HS Code |
108428 |
| Chemical Formula | C7H7ClS |
| Molar Mass | 158.65 g/mol |
| Appearance | Liquid (predicted, as data may vary) |
| Solubility In Water | Low (due to non - polar nature of the aromatic and sulfanyl groups) |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, etc. |
| Vapor Pressure | Low (due to relatively high molar mass and molecular interactions) |
As an accredited 1-Chloro-3-(Methylsulfanyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - chloro - 3 - (methylsulfanyl)benzene in 1 - kg sealed containers for chemical storage. |
| Storage | 1 - Chloro - 3 - (methylsulfanyl)benzene should be stored in a cool, well - ventilated area, away from direct sunlight. Keep it in a tightly closed container, preferably made of corrosion - resistant materials like steel or glass. Store it separate from oxidizing agents and reactive substances to prevent dangerous reactions. Maintain the storage temperature within a moderate range to avoid decomposition. |
| Shipping | 1 - chloro - 3 - (methylsulfanyl)benzene is shipped in tightly - sealed, corrosion - resistant containers. Shipment adheres to strict chemical transport regulations, ensuring proper handling to prevent spills and environmental or safety hazards. |
Competitive 1-Chloro-3-(Methylsulfanyl)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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 1-Chloro-3-(Methylsulfanyl)Benzene in China?
As a trusted 1-Chloro-3-(Methylsulfanyl)Benzene 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 1-Chloro-3-(Methylsulfanyl)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-chloro-3- (methylsulfanyl) benzene?
1 - chloro - 3 - (methylsulfanyl) benzene, the Chinese name is often 3 - methylthiochlorobenzene. The chemical properties of this substance are special.
The chlorine atom on the benzene has a certain activity. In the polychemical reaction, the chlorine atom can be used as a deradical reaction. For example, in the nuclear substitution reaction, if there are suitable nuclei, such as hydroxyl (OH), alkoxy (RO), etc., the chlorine atom can be replaced to form phenol or ether compounds. This is because the chlorine atom is related to benzene, and the density distribution of its sub-cloud is uneven. The effect of the chlorine atom makes the density of the benzene sub-cloud reduce, and it itself has certain properties, so it is vulnerable to nuclear attack.
And its methylthio group (-SCH) is also specialized. In methylthio groups, there are unformed solitary particles outside the sulfur atom, which can exhibit nucleation. In some antibodies, sulfur atoms can attack the center of the missing particles and form new compounds. For example, in the antibodies of methylthio, the sulfur atom of methylthio can replace the sulfur atom of methylthio to form sulfur-containing compounds. In the same way, methylthio groups can also be oxidized, and sulfur atoms can be oxidized to form sulfur or higher oxidized compounds.
Furthermore, benzene from 1-chloro-3 - (methylsulfanyl) benzene can also produce typical aromatic compounds. In the presence of a catalyst, it is possible to replace the inverse group. Due to the high density of the π subcloud of benzene, it is easy to attract the inverse group. For example, in Fu-gram inverse, alkyl or acyl groups can be introduced into the benzene group, and the inverse group is affected by the chlorine atom. In general, the methylthio group is used for the benzene group, and the benzene group has a certain activation effect. The chlorine atom is a weak absorber group, but because it does not share the same subgroup, it can also be used for benzene. It also affects the positioning of the inverse group to a certain extent. Therefore, 1-chloro-3- (methylsulfanyl) benzene exhibits rich chemical properties due to its chlorine atoms, methylthio groups, and benzene properties, and has a useful value in the field of synthesis.
The chlorine atom on the benzene has a certain activity. In the polychemical reaction, the chlorine atom can be used as a deradical reaction. For example, in the nuclear substitution reaction, if there are suitable nuclei, such as hydroxyl (OH), alkoxy (RO), etc., the chlorine atom can be replaced to form phenol or ether compounds. This is because the chlorine atom is related to benzene, and the density distribution of its sub-cloud is uneven. The effect of the chlorine atom makes the density of the benzene sub-cloud reduce, and it itself has certain properties, so it is vulnerable to nuclear attack.
And its methylthio group (-SCH) is also specialized. In methylthio groups, there are unformed solitary particles outside the sulfur atom, which can exhibit nucleation. In some antibodies, sulfur atoms can attack the center of the missing particles and form new compounds. For example, in the antibodies of methylthio, the sulfur atom of methylthio can replace the sulfur atom of methylthio to form sulfur-containing compounds. In the same way, methylthio groups can also be oxidized, and sulfur atoms can be oxidized to form sulfur or higher oxidized compounds.
Furthermore, benzene from 1-chloro-3 - (methylsulfanyl) benzene can also produce typical aromatic compounds. In the presence of a catalyst, it is possible to replace the inverse group. Due to the high density of the π subcloud of benzene, it is easy to attract the inverse group. For example, in Fu-gram inverse, alkyl or acyl groups can be introduced into the benzene group, and the inverse group is affected by the chlorine atom. In general, the methylthio group is used for the benzene group, and the benzene group has a certain activation effect. The chlorine atom is a weak absorber group, but because it does not share the same subgroup, it can also be used for benzene. It also affects the positioning of the inverse group to a certain extent. Therefore, 1-chloro-3- (methylsulfanyl) benzene exhibits rich chemical properties due to its chlorine atoms, methylthio groups, and benzene properties, and has a useful value in the field of synthesis.
What are the physical properties of 1-chloro-3- (methylsulfanyl) benzene?
1-Chloro-3- (methylthio) benzene is one of the organic compounds. Its physical properties are unique and worth exploring.
Looking at its appearance, under normal conditions, 1-chloro-3- (methylthio) benzene is a colorless to light yellow liquid, clear and translucent, like morning dew condensation. This appearance feature makes it easy to identify in many chemical scenes.
Smell its smell, which has a special aromatic smell, but this smell is not pleasant, but has a slightly pungent feeling, just like a warning hidden behind the fragrance. This unique smell is due to the synergistic effect of chlorine atoms and methylthio groups in its molecular structure.
When talking about the boiling point, it is in a certain temperature range, which is a key characteristic of its physical properties. Under normal pressure, its boiling point is specific, so that it exists as a liquid at a specific temperature range. When the temperature gradually rises to the boiling point, the substance changes from the liquid state to the gaseous state, which is a key transition of the material state.
Melting point is also an important physical property. In a specific low temperature environment, 1-chloro-3- (methylthio) benzene will solidify from the liquid state to the solid state, and this melting point defines the critical temperature between its liquid and solid states.
In terms of solubility, 1-chloro-3- (methylthio) benzene is insoluble in water, just like a stranger who is incompatible with water. This is because the hydrogen bond system formed between water molecules does not match the molecular structure of the organic substance. However, it is soluble in organic solvents such as ethanol and ether, just like integrating into the same group, showing good solubility, which is of great significance in the field of organic synthesis.
The density is also the focus of consideration. Its density is different from that of water, which determines the upper and lower stratification when mixed with water. This property is crucial in the actual operation and separation process.
In addition, the vapor pressure of 1-chloro-3- (methylthio) benzene also has a specific value, which is related to its balance between the gas and liquid phases, and has a profound impact on volatility and environmental behavior.
The above physical properties play an indispensable role in chemical synthesis, separation and purification, product storage, etc., helping chemical practitioners to better control this compound.
Looking at its appearance, under normal conditions, 1-chloro-3- (methylthio) benzene is a colorless to light yellow liquid, clear and translucent, like morning dew condensation. This appearance feature makes it easy to identify in many chemical scenes.
Smell its smell, which has a special aromatic smell, but this smell is not pleasant, but has a slightly pungent feeling, just like a warning hidden behind the fragrance. This unique smell is due to the synergistic effect of chlorine atoms and methylthio groups in its molecular structure.
When talking about the boiling point, it is in a certain temperature range, which is a key characteristic of its physical properties. Under normal pressure, its boiling point is specific, so that it exists as a liquid at a specific temperature range. When the temperature gradually rises to the boiling point, the substance changes from the liquid state to the gaseous state, which is a key transition of the material state.
Melting point is also an important physical property. In a specific low temperature environment, 1-chloro-3- (methylthio) benzene will solidify from the liquid state to the solid state, and this melting point defines the critical temperature between its liquid and solid states.
In terms of solubility, 1-chloro-3- (methylthio) benzene is insoluble in water, just like a stranger who is incompatible with water. This is because the hydrogen bond system formed between water molecules does not match the molecular structure of the organic substance. However, it is soluble in organic solvents such as ethanol and ether, just like integrating into the same group, showing good solubility, which is of great significance in the field of organic synthesis.
The density is also the focus of consideration. Its density is different from that of water, which determines the upper and lower stratification when mixed with water. This property is crucial in the actual operation and separation process.
In addition, the vapor pressure of 1-chloro-3- (methylthio) benzene also has a specific value, which is related to its balance between the gas and liquid phases, and has a profound impact on volatility and environmental behavior.
The above physical properties play an indispensable role in chemical synthesis, separation and purification, product storage, etc., helping chemical practitioners to better control this compound.
What are the main uses of 1-chloro-3- (methylsulfanyl) benzene?
1 - chloro - 3 - (methylsulfanyl) benzene, the Chinese name is often 3 - (methylsulfanyl) chlorobenzene. This compound is widely used and is often used in multiple domains.
In the process of synthesis, it plays an important role as a starting material. Researchers often modify and modify it by its specific functionalities, and carefully create biologically active molecules. For example, from a series of reactions, it can be cleverly synthesized by its methylsulfanyl chlorine atoms, which can effectively act on specific biological targets.
In the field, it is also an important cornerstone for the synthesis of multi-efficient molecules. As we all know, it is necessary to have an effective control effect on pests, and the harm to humans and animals in the environment needs to be minimized. 3 - (methylthio) chlorobenzene can be used as the core raw material for the synthesis of new types of active ingredients due to its special chemical properties. Rationalization, the synthesis can precisely act on the specific physiological system of the harm, or inhibit its fertility, or dry its spirit, so as to achieve the desired control effect.
In addition, in the field of materials science, this compound is also useful. Materials scientists have skillfully used its chemical properties to introduce it into the synthesis process of polymer materials. In this way, it can effectively improve some properties of polymer materials, such as improving the resistance of materials, chemical corrosion resistance, etc. For example, in the synthesis of specific engineering plastics, the addition of 3 - (methylthio) chlorobenzene derivatives can enable engineering plastics to maintain good mechanical properties and qualitative properties under high temperature and chemical corrosion conditions, greatly expanding the application of engineering plastics.
, 1 - chloro - 3 - (methylsulfanyl) benzene has indispensable uses in many important fields such as rubber, rubber, and materials.
In the process of synthesis, it plays an important role as a starting material. Researchers often modify and modify it by its specific functionalities, and carefully create biologically active molecules. For example, from a series of reactions, it can be cleverly synthesized by its methylsulfanyl chlorine atoms, which can effectively act on specific biological targets.
In the field, it is also an important cornerstone for the synthesis of multi-efficient molecules. As we all know, it is necessary to have an effective control effect on pests, and the harm to humans and animals in the environment needs to be minimized. 3 - (methylthio) chlorobenzene can be used as the core raw material for the synthesis of new types of active ingredients due to its special chemical properties. Rationalization, the synthesis can precisely act on the specific physiological system of the harm, or inhibit its fertility, or dry its spirit, so as to achieve the desired control effect.
In addition, in the field of materials science, this compound is also useful. Materials scientists have skillfully used its chemical properties to introduce it into the synthesis process of polymer materials. In this way, it can effectively improve some properties of polymer materials, such as improving the resistance of materials, chemical corrosion resistance, etc. For example, in the synthesis of specific engineering plastics, the addition of 3 - (methylthio) chlorobenzene derivatives can enable engineering plastics to maintain good mechanical properties and qualitative properties under high temperature and chemical corrosion conditions, greatly expanding the application of engineering plastics.
, 1 - chloro - 3 - (methylsulfanyl) benzene has indispensable uses in many important fields such as rubber, rubber, and materials.
What are the synthesis methods of 1-chloro-3- (methylsulfanyl) benzene?
For 1-chloro-3- (methylthio) benzene, there are many ways to synthesize it. The following is Ru Chen.
First, take m-chlorobromobenzene and sodium methyl mercaptan as raw materials, add an appropriate amount of solvent, such as N, N-dimethylformamide (DMF), in a suitable reaction vessel. Stir well, heat up to an appropriate temperature, such as 60-80 ° C, and the reaction time. Among them, the halogen atom of m-chlorobromobenzene is active, and the sulfur anion of sodium methyl mercaptan is nucleophilic. The nucleophilic substitution of the two results in 1-chloro-3- (methylthio) benzene. After the reaction is completed, the product is purified by separation and distillation.
Second, start with m-chloroaniline, and first undergo diazotization. Dissolve m-chloroaniline in hydrochloric acid solution, cool to 0-5 ° C, add sodium nitrite solution dropwise to obtain diazonium salt solution. Then, add a methylthio reagent, such as methyl thioethyl acetate, and react under weakly acidic or neutral conditions. The diazo group is replaced by methylthio group, and then hydrolysis and other steps can obtain the target product. This process needs to pay attention to the control of reaction temperature and pH to prevent side reactions.
Third, use m-chlorothiophenol and iodomethane as raw materials. In an alkaline environment, such as an alcoholic solution of potassium carbonate, the thiohydride anion of isochlorothiophenol undergoes a nucleophilic substitution reaction with iodomethane. The reaction is mild and easy to operate. After the reaction, pure 1-chloro-3- (methylthio) benzene can be obtained through extraction, drying, distillation and other processes.
All synthesis methods have advantages and disadvantages. In practical application, when considering the availability of raw materials, cost, difficulty of reaction conditions and other factors, choose the good one and use it.
First, take m-chlorobromobenzene and sodium methyl mercaptan as raw materials, add an appropriate amount of solvent, such as N, N-dimethylformamide (DMF), in a suitable reaction vessel. Stir well, heat up to an appropriate temperature, such as 60-80 ° C, and the reaction time. Among them, the halogen atom of m-chlorobromobenzene is active, and the sulfur anion of sodium methyl mercaptan is nucleophilic. The nucleophilic substitution of the two results in 1-chloro-3- (methylthio) benzene. After the reaction is completed, the product is purified by separation and distillation.
Second, start with m-chloroaniline, and first undergo diazotization. Dissolve m-chloroaniline in hydrochloric acid solution, cool to 0-5 ° C, add sodium nitrite solution dropwise to obtain diazonium salt solution. Then, add a methylthio reagent, such as methyl thioethyl acetate, and react under weakly acidic or neutral conditions. The diazo group is replaced by methylthio group, and then hydrolysis and other steps can obtain the target product. This process needs to pay attention to the control of reaction temperature and pH to prevent side reactions.
Third, use m-chlorothiophenol and iodomethane as raw materials. In an alkaline environment, such as an alcoholic solution of potassium carbonate, the thiohydride anion of isochlorothiophenol undergoes a nucleophilic substitution reaction with iodomethane. The reaction is mild and easy to operate. After the reaction, pure 1-chloro-3- (methylthio) benzene can be obtained through extraction, drying, distillation and other processes.
All synthesis methods have advantages and disadvantages. In practical application, when considering the availability of raw materials, cost, difficulty of reaction conditions and other factors, choose the good one and use it.
What should I pay attention to when storing and transporting 1-chloro-3- (methylsulfanyl) benzene?
1-Chloro-3- (methylthio) benzene, an organic compound, requires careful attention when storing and transporting.
Store first, and choose the environment first. It should be placed in a cool and ventilated place, because the compound is prone to chemical reactions or dangerous when heated. The temperature of the warehouse must be strictly controlled and not too high to prevent its volatilization from accelerating or decomposition. And keep away from fire and heat sources. Open flames and hot topics are taboo because of their flammability. In case of open flames, hot topics or combustion.
Furthermore, the storage place should be kept dry and avoid moisture. Due to moisture or reaction with the compound, its quality and stability are affected. It needs to be stored separately from oxidants, acids, alkalis, etc., and must not be mixed. Because of its contact with these substances, or triggering violent chemical reactions, and even causing serious consequences such as explosions.
As for the packaging, it is also very important. It is necessary to ensure that the packaging is well sealed and there is no risk of leakage. The packaging material should be corrosion-resistant and can resist the erosion of the compound. At the same time, the packaging should be clearly marked with the name of the chemical, hazardous characteristics, emergency treatment measures and other information in order to identify and deal with emergencies.
When transporting, there are also many key points. The transportation vehicle must meet the requirements for the transportation of hazardous chemicals, and be equipped with corresponding fire equipment and leakage emergency treatment equipment. During transportation, it is necessary to prevent exposure to the sun, rain and high temperature. Driving should be stable to avoid bumps and collisions to prevent material leakage due to damaged packaging. And transportation personnel must be professionally trained and familiar with the characteristics of the chemical and emergency treatment methods.
In short, 1-chloro-3- (methylthio) benzene must strictly follow relevant standards and regulations during storage and transportation, regardless of environmental control, packaging requirements, or transportation operation specifications, to ensure personnel safety and the environment are not endangered.
Store first, and choose the environment first. It should be placed in a cool and ventilated place, because the compound is prone to chemical reactions or dangerous when heated. The temperature of the warehouse must be strictly controlled and not too high to prevent its volatilization from accelerating or decomposition. And keep away from fire and heat sources. Open flames and hot topics are taboo because of their flammability. In case of open flames, hot topics or combustion.
Furthermore, the storage place should be kept dry and avoid moisture. Due to moisture or reaction with the compound, its quality and stability are affected. It needs to be stored separately from oxidants, acids, alkalis, etc., and must not be mixed. Because of its contact with these substances, or triggering violent chemical reactions, and even causing serious consequences such as explosions.
As for the packaging, it is also very important. It is necessary to ensure that the packaging is well sealed and there is no risk of leakage. The packaging material should be corrosion-resistant and can resist the erosion of the compound. At the same time, the packaging should be clearly marked with the name of the chemical, hazardous characteristics, emergency treatment measures and other information in order to identify and deal with emergencies.
When transporting, there are also many key points. The transportation vehicle must meet the requirements for the transportation of hazardous chemicals, and be equipped with corresponding fire equipment and leakage emergency treatment equipment. During transportation, it is necessary to prevent exposure to the sun, rain and high temperature. Driving should be stable to avoid bumps and collisions to prevent material leakage due to damaged packaging. And transportation personnel must be professionally trained and familiar with the characteristics of the chemical and emergency treatment methods.
In short, 1-chloro-3- (methylthio) benzene must strictly follow relevant standards and regulations during storage and transportation, regardless of environmental control, packaging requirements, or transportation operation specifications, to ensure personnel safety and the environment are not endangered.
Scan to WhatsApp
