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What are the main uses of 3,5-dibromo-2-aminopyridine?
3,5-Dibromo-2-hydroxyacetophenone is a crucial intermediate in the field of organic synthesis. It is widely used in many industries such as medicine, pesticides, and dyes. Its main uses are listed below:
- ** Pharmaceutical Synthesis **: This compound can be used as a key intermediate for the preparation of a variety of drugs. For example, in the synthesis of some antibacterial drugs, it can be combined with other reagents through specific chemical reactions to form a molecular structure with antibacterial activity. This is due to the bromine atom and hydroxyl group in its molecular structure, which can endow the drug with unique physical and chemical properties and help to improve the drug's ability to inhibit or kill specific bacteria. Or when developing drugs for the treatment of cardiovascular diseases, 3,5-dibromo-2-hydroxyacetophenone can be used as a starting material. After a multi-step reaction, other functional groups can be introduced to shape drug molecules that regulate cardiovascular physiological functions.
- ** Pesticide preparation **: In the field of pesticides, it can be used to synthesize new pesticides. With its structural characteristics, it can participate in the reaction to generate pesticide ingredients that have high toxic effects on pests and have a small impact on the environment. For example, by reacting with nitrogen-containing heterocyclic compounds, pesticides with unique insecticidal mechanisms can be prepared, which can interfere with the nervous system or physiological metabolic processes of pests, and then achieve the purpose of pest control.
- ** Dye manufacturing **: 3,5-dibromo-2-hydroxyacetophenone also plays an important role in dye synthesis. Its structure can participate in the formation of conjugated systems, and the presence of conjugated systems often makes compounds exhibit rich colors. Based on this compound, it can be used to produce various colorful and high-fastness dyes by linking with different chromophore groups, which are widely used in textile, printing and dyeing industries.
What are the synthesis methods of 3,5-dibromo-2-aminopyridine?
The synthesis method of 3,5-dibromo-2-hydroxyacetophenone, as described in ancient books, relies on various chemical techniques and steps.
First, starting with phenols, the target compound can be gradually achieved through halogenation. When phenols meet bromine, under specific reaction conditions, bromine atoms replace hydrogen atoms on the benzene ring in sequence, resulting in halogenated intermediates. This reaction requires careful adjustment of temperature, solvent and reactant ratio to obtain the desired halogenated product. For example, by dissolving phenols in a suitable organic solvent, such as dichloromethane, and slowly dropping bromine at low temperature, the reaction can proceed smoothly, and 3-bromophenol or 3,5-dibromophenol can be obtained, which is the cornerstone for subsequent reactions.
Furthermore, the product of halogenation can be converted into 3,5-dibromo-2-hydroxyacetophenone by acylation. During acylation, acyl halides or acid anhydrides are often used as acylating reagents. Under the catalysis of bases, acyl groups replace the hydrogen of phenolic hydroxyl groups to form a structure in which the carbonyl group is connected to the phenyl ring. If acetyl chloride is used as the acylating agent and pyridine is used as the base, the reaction is stirred at an appropriate temperature, and the hydroxyl group of phenol is combined with the acetyl group, and the final product is obtained.
Another route, or starting from acetophenone, is to introduce bromine atoms by halogenation and then hydroxylation steps. When halogenated, the benzene ring of acetophenone is substituted by bromine atoms under specific conditions to form bromoacetophenone. After hydroxylation, under suitable oxidant and reaction conditions, hydroxyl groups are introduced on the benzene ring, and 3,5-dibromo-2-hydroxyacetophenone can also be synthesized.
However, all synthesis methods require fine regulation of reaction conditions, such as temperature, pH, reaction time, etc., in order to improve the purity and yield of the product. A little carelessness, or side reactions may occur, and the products are mixed, making it difficult to achieve the expected goal.
What is the market price of 3,5-dibromo-2-aminopyridine?
Today there is 3% 2C5-dibromo-2-hydroxyacetophenone, which is a fine chemical raw material, and its market price varies depending on various factors such as quality, supply and demand.
At the quality end, if the purity is very high and the impurities are rare, it can reach the high purity level of the laboratory. Because of the complex preparation process, it takes effort and requires high cost, so the price per gram can reach tens of gold, or even hundreds of gold. Such high purity is mostly used in scientific research experiments, and the accuracy of the composition is strictly required.
When it comes to industrial grade, although the purity is slightly lower than that of high purity products, it still needs to meet specific industrial standards. The price is relatively affordable, measured in kilograms, or hundreds of gold per kilogram. Due to the large scale of industrial production, the cost control is stricter, but it also needs to ensure a certain quality before it can be used in subsequent industrial synthesis and other processes.
Furthermore, the supply and demand situation has a deep impact on its price. If the market demand is strong, such as the pharmaceutical industry's enthusiasm for the research and development of drugs containing this ingredient, or the organic synthesis field's demand for it increases sharply, and the supply is difficult to keep up in time, the price will rise. On the contrary, if the demand is low and the supply is sufficient, the price will decline.
Factors such as origin and transportation costs should not be underestimated. If the origin is far away, the transportation will be disrupted, and the cost will increase, and the price will also increase. And the market competition situation also affects its price. When the competition in the same industry is fierce, in order to compete for market share, the price may be favorable.
In summary, the market price of 3% 2C5-dibromo-2-hydroxyacetophenone fluctuates, ranging from a few gold per gram to hundreds of gold per gram, and about hundreds of gold per kilogram for kilogram-level industrial products. It depends on the specific situation.
What are the precautions for storing and transporting 3,5-dibromo-2-aminopyridine?
For 3,5-dicarboxylic-2-hydroxypyridine, there are several ends that should be paid attention to during storage and transportation.
First heavy packaging. It must be contained in a sealed and suitable container. Because of its specific chemical properties, if the packaging is not dense, it is easy to interact with external air, moisture, etc. For example, moisture intrusion or deliquescence will affect the quality and then damage its effectiveness in subsequent applications. And the packaging material must also be carefully selected, and chemical reactions with the substance should not occur, so as not to cause damage to the packaging and cause the risk of leakage.
Second and environment. Storage must be dry, cool and well ventilated. High temperature can easily cause chemical changes, or even cause bad conditions such as decomposition. And humid environments, as mentioned above, can cause damage to them. Well ventilated can avoid the accumulation of volatile gas and reduce potential safety risks. When transporting, it is also necessary to avoid hot topics and humid places, and prevent violent vibration and collision to prevent package damage.
Furthermore, it is related to isolation. This substance should be stored and transported in isolation from oxidizing and reducing substances, acids and alkalis. Due to its chemical activity, if it comes into contact with the above substances, or triggers violent chemical reactions, such as oxidation-reduction reactions, acid-base neutralization, etc., it will not only damage the structure and properties of 3,5-dicarboxy- 2-hydroxypyridine itself, but also cause serious accidents such as fires and explosions.
In addition, during the storage and transportation process, there must be clear signs indicating its chemical properties, hazard warnings and other key information. In this way, relevant personnel can follow correct procedures when handling to ensure safety. And the storage and transportation conditions should be checked regularly. If the packaging is damaged or the environment is abnormal, appropriate measures should be taken immediately.
What are the physical and chemical properties of 3,5-dibromo-2-aminopyridine?
3,5-Dibromo-2-hydroxyacetophenone is one of the organic compounds. Its physical and chemical properties are unique and have applications in chemical, pharmaceutical and other fields.
In terms of its physical properties, under normal conditions, 3,5-dibromo-2-hydroxyacetophenone is mostly white to light yellow crystalline powder. Looking at its color, it may vary slightly due to the preparation process and purity. This substance has a certain melting point, about 132-136 ° C. The stable melting point is one of the important indicators for identifying its purity. It has little solubility in water, but it can be soluble in some organic solvents, such as ethanol, acetone, chloroform, etc. This difference in solubility is of great significance in its separation, purification and choice of reaction medium.
As for chemical properties, in 3,5-dibromo-2-hydroxyacetophenone, the presence of hydroxyl groups (-OH) and carbonyl groups (C = O) endows it with active chemical activity. Hydroxyl groups can participate in esterification reactions and form corresponding esters with acid compounds under appropriate catalysts and conditions. Carbonyl groups can undergo nucleophilic addition reactions, such as reacting with alcohols to form acetal or semi-acetal structures. At the same time, the bromine atom on the benzene ring also changes its activity due to the influence of ortho-hydroxyl and para-carbonyl groups, which can participate in nucleophilic substitution reactions and be replaced by other functional groups, thus providing the possibility for the synthesis of more complex organic compounds.
Because of its unique physical and chemical properties, 3,5-dibromo-2-hydroxyacetophenone is often used as a drug synthesis intermediate in the pharmaceutical field; in the chemical industry, it can be used to prepare fine chemicals such as special coatings and fragrances.