Linshang Chemical
PRODUCTS
3-Chloro-Benzeneethanamine
Linshang Chemical
|
HS Code |
853603 |
| Chemical Formula | C8H10ClN |
| Molar Mass | 155.624 g/mol |
| Appearance | Typically a colorless to pale yellow liquid |
| Odor | May have a characteristic amine - like odor |
| Solubility In Water | Poorly soluble in water |
| Solubility In Organic Solvents | Soluble in many organic solvents such as ethanol, ether |
| Boiling Point | Approximately 220 - 225 °C |
| Density | Approximately 1.10 - 1.15 g/cm³ |
| Flash Point | Caution: Flammable, flash point in the range relevant for flammable liquids |
As an accredited 3-Chloro-Benzeneethanamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 3 - chloro - benzeneethanamine packaged in a sealed, chemical - resistant bottle. |
| Storage | 3 - chloro - benzeneethanamine should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be kept in a tightly - sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, acids, and bases to prevent chemical reactions. Adequate labeling with relevant hazard information is essential for safety. |
| Shipping | 3 - chloro - benzeneethanamine is shipped in accordance with strict chemical transport regulations. It's typically packed in sealed, corrosion - resistant containers. Shipments are monitored for temperature and safety to prevent leakage and ensure safe delivery. |
Competitive 3-Chloro-Benzeneethanamine 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 3-Chloro-Benzeneethanamine in China?
As a trusted 3-Chloro-Benzeneethanamine 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 3-Chloro-Benzeneethanamine 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-chloro-phenethylamine?
The main use of 3-% -dogwood is at the two ends of its use.
In terms of use, 3-% -dogwood is toxic, tasty and bitter, and has the functions of dissipating cold and relieving pain, reducing inversion and stopping pain, and helping to stop pain. In the road, it is often used to treat the symptoms of cold hernia and abdominal pain. The cold evil coagulates in the liver, causing less abdominal pain, inducing pills and other diseases. With 3-% -dogwood to dissipate cold evil and pass the liver, it can relieve pain. And vomiting disease, if it is caused by the cold of the spleen and stomach, and the inverse of the spleen, 3-% -dogwood can dissipate cold in the middle, reduce inversion and stop pain, so that the spleen and stomach can be reduced, and the vomiting will stop. As for the five more vents, it is mostly due to the decay of the body, and the decay of life and fire, and cannot warm the spleen and soil. 3-% dogwood can help and stop the vents. It is often compatible with other ingredients to reduce this disease.
and taste, 3-% dogwood is also used. Its taste is spicy and has a special fragrance, which can add a special taste to the dishes. The ancient technique of cooking is often used to remove the fishy smell of the meat and make the meat taste more mellow. In some flavored works, adding 3-% dogwood can make the aroma of the taste more mellow, and the next time it is richer. In the cooking of the sea, its spicy nature can remove the cold of the sea, and it can also add the taste, so that the taste buds of the eater can enjoy the taste of the sea.
Therefore, 3-% of the dogwood can be used for disease, and the taste can increase the beauty of the sea. It is a good product with both food and food.
In terms of use, 3-% -dogwood is toxic, tasty and bitter, and has the functions of dissipating cold and relieving pain, reducing inversion and stopping pain, and helping to stop pain. In the road, it is often used to treat the symptoms of cold hernia and abdominal pain. The cold evil coagulates in the liver, causing less abdominal pain, inducing pills and other diseases. With 3-% -dogwood to dissipate cold evil and pass the liver, it can relieve pain. And vomiting disease, if it is caused by the cold of the spleen and stomach, and the inverse of the spleen, 3-% -dogwood can dissipate cold in the middle, reduce inversion and stop pain, so that the spleen and stomach can be reduced, and the vomiting will stop. As for the five more vents, it is mostly due to the decay of the body, and the decay of life and fire, and cannot warm the spleen and soil. 3-% dogwood can help and stop the vents. It is often compatible with other ingredients to reduce this disease.
and taste, 3-% dogwood is also used. Its taste is spicy and has a special fragrance, which can add a special taste to the dishes. The ancient technique of cooking is often used to remove the fishy smell of the meat and make the meat taste more mellow. In some flavored works, adding 3-% dogwood can make the aroma of the taste more mellow, and the next time it is richer. In the cooking of the sea, its spicy nature can remove the cold of the sea, and it can also add the taste, so that the taste buds of the eater can enjoy the taste of the sea.
Therefore, 3-% of the dogwood can be used for disease, and the taste can increase the beauty of the sea. It is a good product with both food and food.
What are the physical properties of 3-chloro-phenethylamine?
3-Bromo-indolebutyric acid is a plant growth regulator. Its physical properties are as follows:
The appearance of this substance is often white to light yellow crystalline powder. Smell it, almost odorless. The melting point is between 154-156 ° C. At this temperature, the substance gradually melts from solid to liquid. The relative density is about 1.52, indicating that it is relatively heavy in the same volume compared with water.
3-Bromo-indolebutyric acid is slightly soluble in water and has a limited degree of solubility in water. However, it is soluble in organic solvents such as ethanol, acetone, and ether, and can be uniformly dispersed in these organic solvents. This solubility property allows it to be formulated into a specific concentration solution with the help of organic solvents in practical applications for application in agricultural production and other fields.
In terms of stability, 3-bromo-indolebutyric acid has certain stability under normal storage and use conditions. However, it is necessary to avoid high temperature, direct light and contact with strong oxidants to prevent chemical reactions such as decomposition, resulting in reduced activity or loss of plant growth. Storage in a suitable environment can better maintain its physical and chemical properties and ensure the use effect.
The appearance of this substance is often white to light yellow crystalline powder. Smell it, almost odorless. The melting point is between 154-156 ° C. At this temperature, the substance gradually melts from solid to liquid. The relative density is about 1.52, indicating that it is relatively heavy in the same volume compared with water.
3-Bromo-indolebutyric acid is slightly soluble in water and has a limited degree of solubility in water. However, it is soluble in organic solvents such as ethanol, acetone, and ether, and can be uniformly dispersed in these organic solvents. This solubility property allows it to be formulated into a specific concentration solution with the help of organic solvents in practical applications for application in agricultural production and other fields.
In terms of stability, 3-bromo-indolebutyric acid has certain stability under normal storage and use conditions. However, it is necessary to avoid high temperature, direct light and contact with strong oxidants to prevent chemical reactions such as decomposition, resulting in reduced activity or loss of plant growth. Storage in a suitable environment can better maintain its physical and chemical properties and ensure the use effect.
What are the chemical properties of 3-chloro-phenethylamine?
3-Bromo-phenylacetamide is an organic compound with unique chemical properties. The following is a brief description of its chemical properties:
1. ** Nucleophilic Substitution Reaction **: In this compound, bromine atoms are highly active and vulnerable to attack by nucleophilic reagents, and then nucleophilic substitution reactions occur. Because bromine atoms are more electronegative than carbon, the electron cloud of the C-Br bond is biased towards the bromine atom, making the carbon atom partially positively charged, and nucleophilic reagents such as hydroxyl (OH) and amino (NH ²) are easily combined with it to replace the bromine atom. For example, when co-heated with an aqueous solution of sodium hydroxide, bromine atoms can be replaced by hydroxyl groups to form a hydroxyl-containing product 3-hydroxy-phenylacetamide, which is often used in organic synthesis to introduce specific functional groups.
2. ** Hydrolysis Reaction **: The amide bond of 3-bromo-phenylacetamide can be hydrolyzed under acid or base catalysis conditions. In acidic conditions, such as heating in dilute hydrochloric acid solution, the amide bond is attacked by water, and gradually hydrolyzed to form 3-bromo-phenylacetic acid and ammonium ions; while in alkaline conditions, such as co-heating with sodium hydroxide solution, the hydrolysis of amide bond produces 3-bromo-phenylacetate and ammonia or amine. Hydrolysis is an important way to prepare carboxylic acid compounds.
3. ** Reaction characteristics of halogenated aromatics **: The bromine atom on the benzene ring decreases the electron cloud density of the benzene ring, which decreases the electrophilic substitution reaction activity of the benzene ring. However, under certain conditions, electrophilic substitution reactions can still occur. For example, in the presence of catalysts such as ferric chloride, it can react with electrophilic reagents such as bromine and nitric acid to introduce new substituents at specific positions in the benzene ring, and because the bromine atom is an ortho-para locator, electrophilic reagents mainly attack its ortho-sites and para-sites.
4. ** Reaction with metal-organic reagents **: 3-bromo-phenylacetamide can react with metal-organic reagents, such as Grignard reagent (RMgX). The carbon-magnesium bond in Grignard reagent is highly polar, and the partially negatively charged carbon can attack the carbonyl carbon of 3-bromo-phenylacetamide to form new carbon-carbon bonds. This reaction is of great significance in the construction of complex organic molecular structures, and can be used to grow carbon chains and introduce specific groups.
1. ** Nucleophilic Substitution Reaction **: In this compound, bromine atoms are highly active and vulnerable to attack by nucleophilic reagents, and then nucleophilic substitution reactions occur. Because bromine atoms are more electronegative than carbon, the electron cloud of the C-Br bond is biased towards the bromine atom, making the carbon atom partially positively charged, and nucleophilic reagents such as hydroxyl (OH) and amino (NH ²) are easily combined with it to replace the bromine atom. For example, when co-heated with an aqueous solution of sodium hydroxide, bromine atoms can be replaced by hydroxyl groups to form a hydroxyl-containing product 3-hydroxy-phenylacetamide, which is often used in organic synthesis to introduce specific functional groups.
2. ** Hydrolysis Reaction **: The amide bond of 3-bromo-phenylacetamide can be hydrolyzed under acid or base catalysis conditions. In acidic conditions, such as heating in dilute hydrochloric acid solution, the amide bond is attacked by water, and gradually hydrolyzed to form 3-bromo-phenylacetic acid and ammonium ions; while in alkaline conditions, such as co-heating with sodium hydroxide solution, the hydrolysis of amide bond produces 3-bromo-phenylacetate and ammonia or amine. Hydrolysis is an important way to prepare carboxylic acid compounds.
3. ** Reaction characteristics of halogenated aromatics **: The bromine atom on the benzene ring decreases the electron cloud density of the benzene ring, which decreases the electrophilic substitution reaction activity of the benzene ring. However, under certain conditions, electrophilic substitution reactions can still occur. For example, in the presence of catalysts such as ferric chloride, it can react with electrophilic reagents such as bromine and nitric acid to introduce new substituents at specific positions in the benzene ring, and because the bromine atom is an ortho-para locator, electrophilic reagents mainly attack its ortho-sites and para-sites.
4. ** Reaction with metal-organic reagents **: 3-bromo-phenylacetamide can react with metal-organic reagents, such as Grignard reagent (RMgX). The carbon-magnesium bond in Grignard reagent is highly polar, and the partially negatively charged carbon can attack the carbonyl carbon of 3-bromo-phenylacetamide to form new carbon-carbon bonds. This reaction is of great significance in the construction of complex organic molecular structures, and can be used to grow carbon chains and introduce specific groups.
What are the synthesis methods of 3-chloro-phenethylamine?
3-Bromo-indolebutyric acid is a plant growth regulator. Although there is no such precise name in ancient techniques, there are traces of plant cultivation methods related to it.
To make this substance, you can prepare it from raw materials. First look for indole and the like. Although there is no name "indole" in the ancient herbal books, there are plant extracts with similar properties or they can be obtained. Extracted by a suitable method, through purification and concentration steps, relatively pure indole raw materials can be obtained.
Take indole and mix it with brominating reagents. In ancient times, there were no modern brominating agents, but the remaining marinade from bromine-containing minerals or seawater sun salts can be specially treated to obtain brominating-like effects. In a suitable container, the temperature and reaction time are controlled so that the bromine atom replaces the hydrogen atom at a specific position of the indole to obtain bromoindole.
Bromoindole is then reacted with the related raw materials of butyric acid. Although there is no pure butyric acid in ancient times, the acidic substance obtained by fermentation can be separated and purified to obtain a substance with similar properties of butyric acid. Bromoindole is mixed with the treated butyric acid-like substance and catalyzed by a specific catalyst. Although there is no modern catalyst in ancient times, some metal salts or special ore powders have been tested or catalyzed. React under suitable conditions to combine the two to form the prototype of 3-bromo-indolebutyric acid.
After the reaction is completed, it needs to go through the process of separation and purification. The ancient methods of filtration, distillation, crystallization, etc. are used to remove impurities and make the product pure. If filtered with fine fabrics, insoluble matter is removed; by distillation, different components are separated according to the difference in boiling point; by crystallization, the product is precipitated in crystal form, resulting in a relatively pure 3-bromo-indolebutyric acid.
Although the ancient method is different from the modern chemical synthesis method, the ancient people also explored the preparation of plant cultivation-related substances with their wisdom, which can provide ideas and reference for today's research.
To make this substance, you can prepare it from raw materials. First look for indole and the like. Although there is no name "indole" in the ancient herbal books, there are plant extracts with similar properties or they can be obtained. Extracted by a suitable method, through purification and concentration steps, relatively pure indole raw materials can be obtained.
Take indole and mix it with brominating reagents. In ancient times, there were no modern brominating agents, but the remaining marinade from bromine-containing minerals or seawater sun salts can be specially treated to obtain brominating-like effects. In a suitable container, the temperature and reaction time are controlled so that the bromine atom replaces the hydrogen atom at a specific position of the indole to obtain bromoindole.
Bromoindole is then reacted with the related raw materials of butyric acid. Although there is no pure butyric acid in ancient times, the acidic substance obtained by fermentation can be separated and purified to obtain a substance with similar properties of butyric acid. Bromoindole is mixed with the treated butyric acid-like substance and catalyzed by a specific catalyst. Although there is no modern catalyst in ancient times, some metal salts or special ore powders have been tested or catalyzed. React under suitable conditions to combine the two to form the prototype of 3-bromo-indolebutyric acid.
After the reaction is completed, it needs to go through the process of separation and purification. The ancient methods of filtration, distillation, crystallization, etc. are used to remove impurities and make the product pure. If filtered with fine fabrics, insoluble matter is removed; by distillation, different components are separated according to the difference in boiling point; by crystallization, the product is precipitated in crystal form, resulting in a relatively pure 3-bromo-indolebutyric acid.
Although the ancient method is different from the modern chemical synthesis method, the ancient people also explored the preparation of plant cultivation-related substances with their wisdom, which can provide ideas and reference for today's research.
What should be paid attention to when storing and transporting 3-chloro-phenethylamine?
3 - It is necessary to pay attention to the following general things in the storage and storage of the waist:
First, the storage environment is very important. It needs to be used in a dry place, because of its damp, the damp is easy to cause corrosion, and its performance and quality. It can be placed in a well-connected building or a storage room, and the temperature should be kept cool, not high, and its active ingredients are easy to dissipate, preferably at 15-25 degrees Celsius.
Second, the packaging should not be ignored. Moisture-proof and opaque packaging materials, such as sealed plastic bags, cans, etc., should be used to prevent external and air intrusion. Before packing, it is necessary to ensure that 3 - the waist has been fully dry, and a lot of water is retained.
Third, it is necessary to prevent bumps and collisions on the way. Because of its crumbling or fragile, it may be broken due to strong shock, which affects the use and phase.
Fourth, avoid the mixing of tasteless things. 3 - The waist is easy to absorb tastiness. If the items with strong tastiness are placed together, they will be contaminated with tastiness, and their original tastiness and products will be damaged.
Fifth, the existing utensils will be polluted. The container may be filled with bacteria, bacteria, etc., to stain the waist and make it raw.
If you want to properly store the waist, you must pay attention to the above, in order to improve the efficacy of its products.
First, the storage environment is very important. It needs to be used in a dry place, because of its damp, the damp is easy to cause corrosion, and its performance and quality. It can be placed in a well-connected building or a storage room, and the temperature should be kept cool, not high, and its active ingredients are easy to dissipate, preferably at 15-25 degrees Celsius.
Second, the packaging should not be ignored. Moisture-proof and opaque packaging materials, such as sealed plastic bags, cans, etc., should be used to prevent external and air intrusion. Before packing, it is necessary to ensure that 3 - the waist has been fully dry, and a lot of water is retained.
Third, it is necessary to prevent bumps and collisions on the way. Because of its crumbling or fragile, it may be broken due to strong shock, which affects the use and phase.
Fourth, avoid the mixing of tasteless things. 3 - The waist is easy to absorb tastiness. If the items with strong tastiness are placed together, they will be contaminated with tastiness, and their original tastiness and products will be damaged.
Fifth, the existing utensils will be polluted. The container may be filled with bacteria, bacteria, etc., to stain the waist and make it raw.
If you want to properly store the waist, you must pay attention to the above, in order to improve the efficacy of its products.
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