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3-Chlorobenzenecarboximidamide Hydrochloride (1:1)
Linshang Chemical
|
HS Code |
506478 |
| Chemical Name | 3-Chlorobenzenecarboximidamide Hydrochloride (1:1) |
| Molecular Formula | C7H8Cl2N2 |
| Molecular Weight | 191.06 g/mol |
| Appearance | Solid |
| Solubility | Soluble in polar solvents like water |
| Melting Point | Typically in a certain range (data needed for exact value) |
| Purity | Can vary depending on source, often high purity for research use |
| Odor | May have a characteristic odor (exact nature needs more data) |
| Storage Conditions | Stored in a cool, dry place away from moisture and incompatible materials |
As an accredited 3-Chlorobenzenecarboximidamide Hydrochloride (1:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 3 - chlorobenzenecarboximidamide Hydrochloride (1:1) in sealed chemical - grade pouch. |
| Storage | 3 - Chlorobenzenecarboximidamide Hydrochloride (1:1) should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and potential reactions. Store it separately from incompatible substances like strong oxidizers or bases to avoid chemical interactions that could degrade the compound or pose safety risks. |
| Shipping | 3 - Chlorobenzenecarboximidamide Hydrochloride (1:1) is shipped in accordance with strict chemical transport regulations. Packed securely in suitable containers, it's transported by carriers experienced in handling such chemicals to ensure safe delivery. |
Competitive 3-Chlorobenzenecarboximidamide Hydrochloride (1:1) prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 3-Chlorobenzenecarboximidamide Hydrochloride (1:1) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of 3-chlorobenzenecarboximidamide Hydrochloride (1:1)?
The chemical structure of 3-chlorobenzamidine hydrochloride (1:1) is one of the structures of organic compounds. Its core part is the benzene ring, which is the basic structure of aromatic hydrocarbons, with special stability and electron cloud distribution. At position 3 of the benzene ring, there are chlorine atoms connected, and the chlorine atoms are electronegative, which can affect the electron cloud density of the benzene ring. The reactivity of the benzene ring is different from that of the unsubstituted one.
And one end of the benzene ring is connected by an imino group (-C = N-), and the nitrogen atom of the imino group is connected with an amino group (-NH ²), which constitutes the amidine group structure. The amidine group has a certain alkalinity and can form salts with acids. In this compound, due to the 1:1 combination with hydrochloric acid, the corresponding hydrochloride salt is formed. The formation of hydrochloride is due to the solitary pair electron-acceptable proton on the nitrogen atom of the amidine group, which binds to the hydrogen ion of hydrochloric acid, resulting in the form of a salt as a whole. This structure makes the compound different from the free base form in terms of solubility and stability. The structure of this compound gives it specific chemical and physical properties, and it may have specific uses and reactivity in the fields of organic synthesis, medicinal chemistry, etc.
And one end of the benzene ring is connected by an imino group (-C = N-), and the nitrogen atom of the imino group is connected with an amino group (-NH ²), which constitutes the amidine group structure. The amidine group has a certain alkalinity and can form salts with acids. In this compound, due to the 1:1 combination with hydrochloric acid, the corresponding hydrochloride salt is formed. The formation of hydrochloride is due to the solitary pair electron-acceptable proton on the nitrogen atom of the amidine group, which binds to the hydrogen ion of hydrochloric acid, resulting in the form of a salt as a whole. This structure makes the compound different from the free base form in terms of solubility and stability. The structure of this compound gives it specific chemical and physical properties, and it may have specific uses and reactivity in the fields of organic synthesis, medicinal chemistry, etc.
What are the physical properties of 3-chlorobenzenecarboximidamide Hydrochloride (1:1)?
3-Chlorobenzamidine hydrochloride (1:1), this is an organic compound. Its physical properties are quite important, and it is related to many chemical and practical application fields.
Looking at its appearance, it is often in the state of white to off-white crystalline powder, which is very useful for compound identification and quality initial judgment. It has good solubility, can be moderately dissolved in some common organic solvents such as methanol and ethanol, and has better solubility in water. This property makes it convenient for solution preparation and chemical reaction medium selection, because a suitable solvent can be selected according to the reaction requirements to promote the reaction.
When it comes to melting point, 3-chlorobenzamidine hydrochloride (1:1) has a specific melting point range. Generally, phase transition occurs at relatively high temperatures, from solid to liquid. Accurate melting point data is of great significance for the determination of the purity of the compound. The higher the purity, the closer the melting point is to the theoretical value. If there is a deviation in the melting point, it may suggest the presence of impurities.
In addition, the chemical properties of this compound are relatively stable at room temperature and pressure. However, when exposed to specific chemical reagents, high temperatures, light and other conditions, chemical reactions may occur, which requires attention during storage and use to avoid contact with substances that can cause it to react. At the same time, store in a cool, dry and dark place to ensure that its quality and performance are not affected. In short, understanding the physical properties of 3-chlorobenzamidine hydrochloride (1:1) is crucial for its application in chemical synthesis, pharmaceutical research and development, and many other fields.
Looking at its appearance, it is often in the state of white to off-white crystalline powder, which is very useful for compound identification and quality initial judgment. It has good solubility, can be moderately dissolved in some common organic solvents such as methanol and ethanol, and has better solubility in water. This property makes it convenient for solution preparation and chemical reaction medium selection, because a suitable solvent can be selected according to the reaction requirements to promote the reaction.
When it comes to melting point, 3-chlorobenzamidine hydrochloride (1:1) has a specific melting point range. Generally, phase transition occurs at relatively high temperatures, from solid to liquid. Accurate melting point data is of great significance for the determination of the purity of the compound. The higher the purity, the closer the melting point is to the theoretical value. If there is a deviation in the melting point, it may suggest the presence of impurities.
In addition, the chemical properties of this compound are relatively stable at room temperature and pressure. However, when exposed to specific chemical reagents, high temperatures, light and other conditions, chemical reactions may occur, which requires attention during storage and use to avoid contact with substances that can cause it to react. At the same time, store in a cool, dry and dark place to ensure that its quality and performance are not affected. In short, understanding the physical properties of 3-chlorobenzamidine hydrochloride (1:1) is crucial for its application in chemical synthesis, pharmaceutical research and development, and many other fields.
What is 3-chlorobenzenecarboximidamide Hydrochloride (1:1)?
3-Chlorobenzamidine hydrochloride (3-chlorobenzenecarboximidamide + Hydrochloride (1:1)) has a wide range of uses. In the field of medicine, it is an important organic synthesis intermediate. It can be used to create a variety of drugs, such as some antibacterial drugs. With its special chemical structure, it participates in the construction of drug molecules to achieve specific pharmacological effects.
In the chemical industry, it is often used as a key raw material for the synthesis of functional materials. Because of its chlorine atom and amidine structure, it can endow materials with unique chemical properties, such as improving the stability and reactivity of materials, and then used to prepare polymers with special properties.
It also has important value in the development of agricultural chemicals. Or it can be used as a starting material for the synthesis of new pesticides. With its chemical properties, pesticides have better insecticidal and bactericidal activities, and help in the control of agricultural pests and diseases.
And because its structure contains specific functional groups, it is often used in organic chemistry research to explore new chemical reaction paths and mechanisms, providing assistance for the development of organic synthetic chemistry and promoting progress in the field of chemical science.
In the chemical industry, it is often used as a key raw material for the synthesis of functional materials. Because of its chlorine atom and amidine structure, it can endow materials with unique chemical properties, such as improving the stability and reactivity of materials, and then used to prepare polymers with special properties.
It also has important value in the development of agricultural chemicals. Or it can be used as a starting material for the synthesis of new pesticides. With its chemical properties, pesticides have better insecticidal and bactericidal activities, and help in the control of agricultural pests and diseases.
And because its structure contains specific functional groups, it is often used in organic chemistry research to explore new chemical reaction paths and mechanisms, providing assistance for the development of organic synthetic chemistry and promoting progress in the field of chemical science.
What is the synthesis method of 3-chlorobenzenecarboximidamide Hydrochloride (1:1)?
The synthesis of 3-chlorobenzamidine hydrochloride (1:1) is an important issue in the field of organic synthesis. The synthesis steps often have many considerations, because in order to obtain pure and high-yield products, the reaction conditions need to be carefully adjusted.
First, suitable starting materials can be selected. 3-chlorobenzonitrile is often used as the initial material, because its structure can be converted into amidine groups through specific reactions. This conversion process can be achieved by reacting with ammonia or amine compounds under suitable conditions.
Temperature is a key factor in the control of reaction conditions. If the temperature is too high, it may cause a cluster of side reactions, and the purity of the product will be damaged; if the temperature is too low, the reaction rate will be delayed and take a long time. Usually, this reaction is carried out under moderate heating conditions, between about 50 ° C and 100 ° C, depending on the reaction system.
Furthermore, the choice of solvent should not be underestimated. Good solvents need to be able to dissolve raw materials and products without adverse effects on the reaction process. Solvents such as alcohols, ethers or halogenated hydrocarbons can be used in this reaction system, depending on the raw materials and reaction characteristics.
In addition, the addition of catalysts may accelerate the reaction rate. Some metal salts or organic bases may act as catalysts for this reaction, facilitating the smooth conversion of cyanyl groups to amidine groups.
After the reaction is completed, the separation and purification of the product is also important. The target product 3-chlorobenzamidine hydrochloride can be separated from the reaction mixture by means of recrystallization, column chromatography, etc., to achieve high purity requirements. Through this step, 3-chlorobenzamidine hydrochloride (1:1) can be effectively synthesized.
First, suitable starting materials can be selected. 3-chlorobenzonitrile is often used as the initial material, because its structure can be converted into amidine groups through specific reactions. This conversion process can be achieved by reacting with ammonia or amine compounds under suitable conditions.
Temperature is a key factor in the control of reaction conditions. If the temperature is too high, it may cause a cluster of side reactions, and the purity of the product will be damaged; if the temperature is too low, the reaction rate will be delayed and take a long time. Usually, this reaction is carried out under moderate heating conditions, between about 50 ° C and 100 ° C, depending on the reaction system.
Furthermore, the choice of solvent should not be underestimated. Good solvents need to be able to dissolve raw materials and products without adverse effects on the reaction process. Solvents such as alcohols, ethers or halogenated hydrocarbons can be used in this reaction system, depending on the raw materials and reaction characteristics.
In addition, the addition of catalysts may accelerate the reaction rate. Some metal salts or organic bases may act as catalysts for this reaction, facilitating the smooth conversion of cyanyl groups to amidine groups.
After the reaction is completed, the separation and purification of the product is also important. The target product 3-chlorobenzamidine hydrochloride can be separated from the reaction mixture by means of recrystallization, column chromatography, etc., to achieve high purity requirements. Through this step, 3-chlorobenzamidine hydrochloride (1:1) can be effectively synthesized.
What are the safety precautions for 3-chlorobenzenecarboximidamide Hydrochloride (1:1)?
3-Chlorobenzamidine hydrochloride (1:1) is a chemical substance. Regarding its safety precautions, the following points need to be carefully checked:
First, this substance is potentially irritating. If it accidentally touches the skin, it should be rinsed with a large amount of water immediately and continued for a period of time to ensure that there is no residue. If you still feel unwell after rinsing, be sure to seek medical attention immediately. If it comes into contact with the eyes, it is even more critical. You need to open the eyelids immediately, rinse them thoroughly with flowing water or normal saline, and then go to the hospital as soon as possible to be treated by a professional. Do not delay to avoid serious and irreversible damage to the eyes.
Second, inhaling this substance is also risky. In the environment containing this substance, it is necessary to ensure good ventilation, and it is best to carry out relevant operations in a fume hood. If you inhale it accidentally, you should immediately move it to a fresh air place to keep the respiratory tract unobstructed. If you have symptoms such as breathing difficulties, you should give oxygen in time and send it to a doctor for first aid as soon as possible without any delay.
Third, you should also be vigilant in the case of accidental ingestion. If you accidentally ingest it, do not induce vomiting by yourself. You should seek medical attention immediately and bring relevant information about the substance, so that the doctor can accurately judge and take appropriate treatment measures.
Fourth, you should also pay attention to storage. Store it in a cool, dry and well-ventilated place, away from fire and heat sources. At the same time, it should be stored separately from oxidants, acids, etc., and must not be mixed to prevent dangerous chemical reactions.
In short, when using 3-chlorobenzamidine hydrochloride (1:1), it is necessary to strictly follow the safety operating procedures and take good personal protection, such as wearing appropriate protective gloves, protective glasses and masks, to maximize personal safety and environmental safety.
First, this substance is potentially irritating. If it accidentally touches the skin, it should be rinsed with a large amount of water immediately and continued for a period of time to ensure that there is no residue. If you still feel unwell after rinsing, be sure to seek medical attention immediately. If it comes into contact with the eyes, it is even more critical. You need to open the eyelids immediately, rinse them thoroughly with flowing water or normal saline, and then go to the hospital as soon as possible to be treated by a professional. Do not delay to avoid serious and irreversible damage to the eyes.
Second, inhaling this substance is also risky. In the environment containing this substance, it is necessary to ensure good ventilation, and it is best to carry out relevant operations in a fume hood. If you inhale it accidentally, you should immediately move it to a fresh air place to keep the respiratory tract unobstructed. If you have symptoms such as breathing difficulties, you should give oxygen in time and send it to a doctor for first aid as soon as possible without any delay.
Third, you should also be vigilant in the case of accidental ingestion. If you accidentally ingest it, do not induce vomiting by yourself. You should seek medical attention immediately and bring relevant information about the substance, so that the doctor can accurately judge and take appropriate treatment measures.
Fourth, you should also pay attention to storage. Store it in a cool, dry and well-ventilated place, away from fire and heat sources. At the same time, it should be stored separately from oxidants, acids, etc., and must not be mixed to prevent dangerous chemical reactions.
In short, when using 3-chlorobenzamidine hydrochloride (1:1), it is necessary to strictly follow the safety operating procedures and take good personal protection, such as wearing appropriate protective gloves, protective glasses and masks, to maximize personal safety and environmental safety.
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