Qiji Chemical
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2-Bromobutane

Qiji Chemical

2-Bromobutane
Specifications

HS Code

484472

Chemical Formula C4H9Br
Molar Mass 137.02 g/mol
Appearance Colorless to light yellow liquid
Odor Characteristic sweet, ether - like odor
Density 1.258 g/cm³ at 20 °C
Boiling Point 91 - 92 °C
Melting Point -112 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in ethanol, ether, chloroform, etc.
Flash Point 18 °C
Refractive Index 1.4368 at 20 °C
Packing & Storage
Packing 100 mL of 2 - Bromobutane in a tightly - sealed glass bottle for safe storage.
Storage 2 - Bromobutane should be stored in a cool, well - ventilated area, away from heat sources and open flames as it is flammable. Keep it in a tightly sealed container to prevent vapor leakage. Store it separately from oxidizing agents and strong bases to avoid potentially dangerous reactions. This storage method helps maintain its stability and safety.
Shipping 2 - Bromobutane is a hazardous chemical. Shipping requires proper packaging in UN - approved containers. It must be labeled clearly with hazard warnings. Transport follows regulations for flammable and toxic substances to ensure safety.
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2-Bromobutane 2-Bromobutane
General Information
Historical Development
Since modern times, the technology of chemistry has become increasingly new, and many compounds have been created. 2-Bromobutane has also emerged in the process of chemical evolution.
At the beginning, chemists studied the reaction mechanism of halogenated hydrocarbons and explored the formation path of halogenated alkanes under different conditions in various experiments. After repeated attempts, 2-Bromobutane was gradually prepared by co-heating butanol and hydrobromic acid. During this process, the reaction temperature, the proportion of reactants, and the selection of catalysts were adjusted and optimized countless times.
With the passage of time, chemical technology has improved, from small-scale preparation in the laboratory to industrial production. Reaction kinetics and thermodynamics have been studied in depth, and the process has been improved to increase the yield and purity of 2-Bromobutane. This compound has been widely used in the field of organic synthesis, providing key raw materials for the synthesis of many fine chemicals such as drugs and fragrances, leaving a strong mark on the history of chemical development.
Product Overview
2 - Overview of Bromobutane Products
2 - Bromobutane, the chemical formula is\ (C_ {4} H_ {9} Br\), which is one of the most common compounds. Its outer color is yellow to light color, and it has a special taste and good performance.
The synthesis of this substance is often obtained by n-butanol bromide under the catalysis of sulfuric acid. In contrast, n-butanol bromide is replaced by bromine atoms to form 2-Bromobutane.
2 - Bromobutane is active, and it is easy to generate nuclear substitution in the chemical compound. The bromine atom is disposed by other nuclei. If oxidized in aqueous solution, 2-butanol can be generated; cyanide can be reversed, and valeronitrile can be obtained. It can also eliminate the reaction. Under the action of alcoholic oxidation, it can be debrominated to form butenes.
It has a wide range of uses in the synthesis of synthetic fields, and can be used in the synthesis of polymers, fragrances and other compounds. Such as the synthesis of a chemical compound, an important starting material for 2-bromobutane, and a multi-step reaction. Molecular skeleton.
Physical & Chemical Properties
2 - Bromobutane is also an organic compound. Its physical and chemical properties can be investigated quite well. Looking at its physical properties, at room temperature, it is a colorless and transparent liquid with a special odor. Its boiling point is about 101.6 ° C, and its density is heavier than water, about 1.258g/cm ³. It is insoluble in water, but it can be miscible with organic solvents such as alcohols and ethers.
When it comes to chemical properties, the bromine atom in 2 - Bromobutane is quite active. When encountering nucleophiles, it is easy to initiate nucleophilic substitution reactions. For example, when co-heated with an aqueous solution of sodium hydroxide, the bromine atom is replaced by a hydroxyl group to form 2 - butanol. If co-heated with an alcohol solution of potassium hydroxide, an elimination reaction occurs to form butene compounds. This is because in its molecular structure, bromine atoms are affected by electron clouds of neighboring carbon atoms, and the density of electron clouds changes, causing their reactivity to be highlighted. They are widely used in the field of organic synthesis.
Technical Specifications & Labeling
2 - Bromobutane is also an organic compound. The technical specifications and identification (product parameters) for its preparation are quite important. The preparation method is usually obtained by co-heating butanol and hydrobromic acid through substitution reaction. During the reaction, the temperature control and the proportion of ingredients must be accurate.
In the technical specifications, the reaction vessel must be clean and dry to prevent impurities from disturbing it. The temperature should be maintained in a suitable range. If it is too high, side reactions will be raw, and if it is too low, the reaction will be slow.
In terms of identification (product parameters), the purity of the product should be clear, and the content of 2 - Bromobutane should reach a certain standard. And its physical properties, such as boiling point, density, etc., also need to be specified. In this way, the quality of the product can be guaranteed and it can be properly applied in various fields of chemical industry.
Preparation Method
To prepare 2-Bromobutane, the raw materials, production process, reaction steps and catalytic mechanism are as follows. The main raw materials are n-butanol and hydrobromic acid, mixed in a flask, and an appropriate amount of sulfuric acid is added as a catalyst. The reaction step is to pour n-butanol into the flask, slowly inject hydrobromic acid, and then add sulfuric acid dropwise, and heat to promote the reaction. This is a nucleophilic substitution reaction mechanism, where the hydroxyl group is replaced by bromine ions. The reaction process needs to be temperature controlled, and the side reactions should not be caused by excessive temperature. After the reaction is completed, pure 2-Bromobutane can be obtained through the steps of separation, washing and drying. In this way, the operation is simpler and the yield can be observed.
Chemical Reactions & Modifications
In the process of nuclear substitution, the atom is easily replaced by the nucleus. In case of an aqueous solution of oxidation, the atom is radicalized to obtain 2-butanol. This reaction rate is affected by the degree of solubility and solubility.
It is also necessary to eliminate the reaction. If the alcohol solution is oxidized, it will be debrominated to form a butene.
If the reaction orientation is checked, the polygenic substituent is more alkene.
To achieve its properties, the reaction parts can be repaired. The overall solubility can be improved and the nuclear substitution can be eliminated. Reducing solubility helps to eliminate inversion; on the contrary, it promotes nuclear substitution. And the degree is also low, high-quality elimination, and low-quality partial substitution. All this is important to control the inversion of 2-Bromobutane.
Synonyms & Product Names
2 - Bromobutane is also an organic compound. Its synonym and trade name are quite important to chemical learners.
This compound has its specific chemical structure and properties. In the heteronym, either according to its structural characteristics or according to the traditional naming method. The trade name is related to production and market circulation.
In the field of chemical research, knowing the synonym and trade name of 2 - Bromobutane helps to communicate accurately and avoid ambiguity. The synonym can show its chemical characteristics from different angles, and the trade name often involves commercial use and brand identity.
Chemists, when discussing 2-Bromobutane, must study its synonyms and trade names in detail, in order to be able to use it correctly in experiments and production, and to promote the progress of chemistry.
Safety & Operational Standards
2 - The safety of Bromobutane operation
2 - Bromobutane is a commonly used item in chemical research, and it is well known that its safety and operation are of paramount importance to ensure the safety and safety of people.
#1. The importance of survival
2 - Bromobutane is suitable for high quality and good quality. Because of its safety, if it is stored in high quality or impassable places, it is easy to cause fatigue, increase fire and explosion. And Fire source, oxidation, etc., to prevent strong reaction.
#2. Operation
Operation 2 - Bromobutane, must be combined to prevent. Those who need to wear clothing, wear anti-gloves and eyes. Due to the irritation of the skin and eyes, it is not necessary to connect it accidentally.
It is also difficult to operate in the passageway. 2 - Bromobutane. If it is not in the room, it will be inhaled, which is harmful to health. The passageway can effectively drain the air and reduce the air temperature.
The operation method must be careful. Remove 2 - Bromobutane. A dropper or pipette should be used to prevent it from leaving. Pour slowly and the container mouth is broken to avoid falling off.
#3. If the skin is accidentally connected to 2 - Bromobutane, wash it with plenty of water immediately, and then clear it with soap. If the eyes are connected, wash with physiological water or water immediately.
In case of leakage, cut the ignition source first to avoid human leakage. Small leakage can be collected with adsorption materials such as sand and vermiculite; large leakage needs to be plugged, and then dealt with by the method.
Of course, 2 - The safe operation of Bromobutane should not be ignored. Only those who comply with the standard can effectively avoid leakage and benefit from research.
Application Area
2 - Bromobutane is also an organic compound. Its application field is quite wide. In the field of organic synthesis, it is often used as an alkylation reagent. It can react with many nucleophiles to form carbon-carbon bonds or carbon-heteroatomic bonds to form a variety of complex organic molecules, which is of great significance in the field of medicinal chemistry. In pharmaceuticals, the reaction of 2 - Bromobutane can be used to synthesize drug molecules with specific biological activities, or as key intermediates.
Furthermore, it is also useful in the field of materials science. It can be introduced into the polymer structure through specific reactions to improve the properties of polymers, such as solubility and thermal stability, providing a way to create new functional materials. From this perspective, 2 - Bromobutane plays an indispensable role in the application fields of organic synthesis and materials science, and contributes greatly to the development of related disciplines and industrial production.
Research & Development
I am dedicated to the research of 2-Bromobutane. This compound has a unique structure and interesting properties. I began to explore its reaction mechanism and observe its changes under different conditions in detail. After repeated experiments, it was found that when it participated in the nucleophilic substitution reaction, the different conditions would lead to product differences. When it was high temperature and strong alkalinity, the reaction tended to eliminate the reaction, while under mild conditions, nucleophilic substitution was more likely to occur.
During the study, I also paid attention to the optimization of its synthesis path. After many attempts, a more efficient method was found, which could increase the yield and reduce the generation of by-products. This achievement is expected to lay the foundation for the industrial production of 2-Bromobutane, promote its wider application in the field of organic synthesis, and promote the development of related industries.
Toxicity Research
Recently, I studied the product of 2-Bromobutane in the room. This product is also an organic halide, and it is quite important to observe its toxicity.
At the beginning, observe its chemical properties, and know that it interacts with other things, or changes. It enters the body, or interacts with the plasticity of cells, causing physiological chaos. I study it with various methods to observe its effect on living things. Take small animals as an experiment, put an appropriate amount of 2-Bromobutane, and observe its condition. See the beast under test, there are signs of restlessness and fatigue, and it can be seen that this product is disturbing to living things.
And explore its poison in the environment. Scattered outside, or into the water and soil, it is a disaster to the ecology. Over time, or accumulated in the body of organisms, move up the food chain, and cause widespread harm. Therefore, the toxicity of Research 2-Bromobutane is essential for the protection of people and ecology, and cannot be ignored.
Future Prospects
I will study the product of 2 - Bromobutane and think about its future prospects. This substance has great potential in the way of organic synthesis. Its unique structure can open many reaction paths.
To see the future of husband, or to emerge in the field of pharmaceutical creation. Based on it, it may be able to derive special effects of drugs, cure various diseases, and solve the suffering of the world. It is also expected to shine in the field of material science, help the birth of new materials, and contribute to industrial progress.
Although there may be thorns in the road ahead, the road of scientific exploration lies in moving forward bravely. When we study diligently, we will use the hidden wonders of Kai 2-Bromobutane in the future to benefit the academic community and the world, and live up to the mission of scientific research.
Frequently Asked Questions
What are the physical properties of 2-bromobutane?
2-% cyanoethylfuran is an organic compound with unique physical properties. Its properties are colorless to light yellow liquid, which exists stably at room temperature and pressure.
Looking at its appearance, colorless to light yellow liquid, clear and transparent, without obvious impurities, this is an intuitive physical characteristic.
Smell the smell, often has a special irritating smell, although not foul odor and unpleasant smell, it has a certain degree of irritation. When operating, pay attention to the ventilation environment to avoid discomfort to the human respiratory tract.
When it comes to boiling point, 2-% cyanoethylfuran has a relatively high boiling point. This property causes it to boil into a gaseous state at a higher temperature. In the field of organic synthesis, boiling point characteristics are related to material separation and purification operations.
In addition to the melting point, the melting point is relatively low, and it is in a liquid state at room temperature, which is convenient for direct use as a reaction solvent or as a raw material for participating in the reaction under most reaction conditions.
2-% cyanoethylfuran density is different from water, generally slightly larger than water. When it comes to liquid-liquid mixing and other operations, the density difference can cause stratification phenomenon, which can be used to realize preliminary separation and other operations.
In terms of solubility, it can be soluble in some organic solvents, such as ethanol, ether, etc. This property makes it possible to select a suitable solvent system according to the reaction requirements in organic synthesis to promote the smooth progress of the reaction and improve the reaction yield and selectivity.
Its volatility is relatively low, and it is not easy to evaporate quickly into the air, which reduces the loss and safety risk caused by volatilization during storage and use, and ensures a stable operating environment.
Overall, the physical properties of 2-% cyanoethylfuran are of great significance in the fields of organic synthesis, chemical production, etc., and have a profound impact on its application methods and process conditions.
What are the chemical properties of 2-bromobutane?
Dicyanoanthraquinone is an important raw material for organic synthesis and is widely used in the chemical industry. Its chemical properties are unique, with the following ends:
First, it has strong oxidation. The quinone structure of dicyanoanthraquinone makes it easy to obtain electrons and is oxidizing. In a specific chemical reaction, it can oxidize other substances and be reduced by itself. This property is often used in oxidation reactions to promote the reaction process and synthesize specific products.
Second, it has a conjugate system. Its molecular structure contains a large conjugate system, which gives it certain stability and special optical properties. The conjugate system delocates the intra-molecular electrons, reduces the molecular energy and improves the stability. At the same time, due to the conjugation effect, dicyanoanthraquinone has specific absorption in the ultraviolet-visible region, showing unique color and optical properties.
Third, it has electrophilic substitution activity. The electron cloud density at some positions in the molecule is relatively low, which is vulnerable to the attack of electrophilic reagents and occurs electrophilic substitution reaction. This reactivity provides the possibility for the introduction of different functional groups. Through electrophilic substitution, dicyanoanthraquinone can be structurally modified to synthesize a series of derivatives and expand its application in different fields.
Fourth, it has certain stability to acid and base. Under common acid and base conditions, the chemical structure of dicyanoanthraquinone is relatively stable, and it is not easy to hydrolyze or other destructive reactions. However, under strong acid and alkali or specific catalytic conditions, corresponding chemical reactions may occur, or molecular structures may be changed, or new reaction pathways may be involved.
In short, dicyanoanthraquinone has shown important value and broad application prospects in many fields such as organic synthesis and materials science due to its chemical properties such as oxidation, conjugation system, electrophilic substitution activity and acid-base stability.
What are the common synthesis methods of 2-bromobutane?
The common synthesis methods of 2-% nitrile pyridine are described in the paradigm of "Tiangong Kaiwu" as follows:
First, pyridine is used as a group and is replaced by electrophilic substitution. The pyridine ring has the characteristics of electron cloud distribution and can interact with electrophilic reagents under specific conditions. If an appropriate halogenating agent is used, a halogen atom is first introduced into the pyridine ring, and then a cyanide group is used to replace the halogen. This process requires attention to the control of the reaction conditions, the temperature during halogenation, the proportion of reagents, and the activity and reaction environment of the cyanide reagents in the cyanide step to prevent side reactions and low yields.
Second, the coupling reaction catalyzed by metal. Select suitable metal catalysts, such as palladium, nickel, etc., with specific ligands. Halopyridine derivatives and cyanyl sources, such as zinc cyanide, potassium cyanide, etc., are used under the action of the catalyst to realize the construction of carbon-cyanide bonds. This approach requires quite strict requirements on the purity of the reaction system, the activity and stability of the catalyst. The amount of catalyst and the choice of reaction solvent are all related to the success or failure of the reaction and the efficiency.
Third, the formaldehyde or ketone is used as the starting material and synthesized through a multi-step reaction. First, the aldehyde or ketone is synthesized with ammonia and a specific nitrile reagent in a suitable acid-base environment. After a series of reactions such as condensation and cyclization, the pyridine ring is constructed and the nitrile group is introduced. The steps of this synthesis path are complicated, but the precise control of the product structure can be achieved by fine-tuning the selection of starting materials and reaction conditions. The intermediates in each step of the reaction need to be properly separated and purified to avoid the accumulation of impurities and affect the quality and yield of the final product.
All synthesis methods have advantages and disadvantages. In practical application, when considering the availability of raw materials, the cost of the reaction, the purity and yield of the product, etc.
What are the applications of 2-bromobutane in organic synthesis?
2-% hydroxyethyl imidazole has many applications in organic synthesis. Although this specific compound was not specifically discussed in "Tiangong Kaiwu", its possible uses can be inferred based on the wisdom and chemical technology of the application of chemical substances in ancient times.
In organic synthesis, 2-% hydroxyethyl imidazole is often used as a catalyst. Because its structure contains nitrogen atoms, it has a certain alkalinity and can effectively catalyze specific chemical reactions. For example, in some esterification reactions, it can promote the reaction of carboxylic acids and alcohols, and improve the reaction rate and yield. This is like the ancient alchemists or craftsmen who used certain additives to improve the process effect when refining medicinal pills and building utensils.
Furthermore, 2-% hydroxyethyl imidazole can be used as a ligand. In the field of metal-organic chemistry, it can coordinate with metal ions to form complexes. This complex may have unique catalytic properties and is used for specific organic reactions. This is similar to the ancients who knew that the combination of different substances can produce unique effects. In metallurgy or dyeing processes, different materials are combined to achieve the desired quality.
In addition, 2-% hydroxyethyl imidazole is also used in material synthesis. It can participate in polymer synthesis and give materials special properties. For example, when preparing some functional polymer materials, it is introduced into the polymer chain, or the material has better hydrophilicity and thermal stability. Just like the ancients when dyeing fabrics or firing ceramics, adding special substances to change the properties of materials to meet the needs of life or process. Overall, 2-% hydroxyethyl imidazole plays an important role in many aspects of organic synthesis, just like various process aids in ancient times, helping to achieve specific chemical conversions and material properties optimization.
What are the precautions in the preparation of 2-bromobutane?
The method of making bait is related to the success or failure of fishing, especially the two-in-one earthworm bait. When making this bait, all details must be paid attention to.
The choice of the first heavy earthworm. When choosing a fresh and fat one, its color is bright and powerful. These earthworms are full of vitality, can release a strong fishy smell, and have a good effect on luring fish. If the earthworm is weak and the fishy smell is weak, it is difficult to lure the fish to the hook.
This is the preparation of the bait. Take an appropriate amount of earthworms and place them in a clean vessel. Break them into several pieces, not too broken, to maintain their shape. Add a little spice, or honey, or clove juice to increase the taste of the bait. The amount of spice must be pinched accurately. If it is too much, the taste will be flushed, and the fish will be repelled; if it is too little, the taste will be weak, and it will be difficult to attract the attention of the fish.
Furthermore, the preservation of the bait should not be underestimated. The prepared bait should be placed in a cool place to prevent it from deteriorating. If the weather is hot, the bait can be placed in an ice box to delay its decay. When using, gently pinch the bait on the hook to ensure that the bait is tightly attached to the hook body and does not fall off easily when entering the water.
When stirring, the method is also exquisite. Stir it slowly, so that the earthworms and the spice are fully integrated, and the taste is uniform but not dissipated. And the stirring speed should not be fast, so as not to hurt the earthworms,
To make two-in-one earthworm bait, you need to be careful from the selection of earthworms to the preparation, preservation and stirring. All kinds of links are interconnected, and a slight difference will affect the fishing performance. Only with caution can you make good bait and get something out of fishing.