3-N-BUTYLTHIOPHENE 98+%

3-N-butylthiophene, with a content of more than 98%, is one of the organic compounds. This compound is formed by linking the thiophene ring to the butyl group, and its position is quite important in the field of organic synthesis.
For this substance, in terms of structure, the thiophene ring is aromatic, and the butyl group is alkyl. The connection between the two gives this compound unique physical and chemical properties. Its physical properties, at room temperature, or in a liquid state, have specific boiling points, melting points and densities. Chemically, due to the presence of thiophene rings, electrophilic substitution reactions can occur, such as halogenation, nitrification, sulfonation, etc. The introduction of butyl may affect the activity and selectivity of the reaction.
In organic synthesis, 3-N-butylthiophene can be used as a key intermediate. For example, in the preparation of functional materials, it can be converted into materials with photoelectric properties through specific chemical reactions, which have potential applications in organic Light Emitting Diodes (OLEDs), solar cells and other fields. Due to the rise of organic semiconductor materials, such compounds containing thiophene structures have attracted much attention due to their good charge transport properties and stability.
In addition, in the field of medicinal chemistry, 3-N-butylthiophene may also be used as a starting material to construct bioactive molecular structures through a series of reactions, providing a new way for the development of new drugs.
In short, although 3-N-butylthiophene is only an organic compound, it has shown important value and application potential in many fields due to its unique structure and diverse properties.

3-N-butylthiophene, with a content of more than 98%, has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. It can be cleverly combined with other compounds through specific chemical reactions to prepare organic materials with complex structures and specific properties. These organic materials have significant uses in the field of optoelectronics. For example, when manufacturing organic Light Emitting Diodes (OLEDs), 3-N-butylthiophene-derived materials can optimize the luminous efficiency and stability of the device, making the display screen clearer and more colorful.
It can also play an important role in the preparation of polymer materials. Through polymerization, 3-N-butylthiophene can participate in the construction of the main chain or side chain structure of the polymer, giving the polymer material unique electrical, optical or thermal properties. For example, the preparation of conductive polymer materials can improve the electrical conductivity of the material, which has potential applications in electronic devices, sensors and other fields, and can improve the sensitivity and selectivity of the sensor to detect specific substances.
At the level of scientific research and exploration, 3-N-butylthiophene is used as a model compound to help researchers deeply explore the reaction mechanism and performance laws of thiophene compounds. By studying its chemical reaction process and product characteristics, it provides theoretical basis and practical guidance for the development of new organic synthesis methods and the design of better functional materials, and promotes the continuous development of organic chemistry, materials science and other disciplines.

3-N-butylthiophene, with a content of more than 98%. Its physical properties are as follows:
This substance is mostly liquid at room temperature, and the appearance is clear and has a specific flowing state. The color may be nearly colorless, or very light yellowish, and the pure one is almost transparent, without obvious variegation or turbidity. Smell, with a special smell, although not pungent and intolerable, it is also different from ordinary odorless things and has its own unique smell identification.
Its boiling point is a specific value. At this temperature, the substance changes from liquid to gaseous state. This boiling point is one of the important physical markers of the substance and can be used for separation, purification and other processes. The melting point is also a specific value. When the temperature drops below the melting point, a substance solidifies from a liquid state to a solid state. The characteristics of this melting point need to be considered in detail when storing, transporting, and specific process applications. The density of
3-N-butylthiophene is different from that of water. In some application scenarios, this density difference is related to the distribution of the substance in the mixed system. For example, in the process of liquid-liquid extraction, it is layered with other liquids by virtue of the density difference, and then the purpose of separation is achieved. Its solubility is also an important characteristic. It is soluble in some organic solvents. This characteristic determines that in the organic synthesis reaction, a suitable solvent can be selected to promote the smooth progress of the reaction and enhance the contact and reaction efficiency of the reactants. In addition, its refractive index and other optical properties are also unique. In applications in related fields such as optical materials, the characteristics of refractive index may play a key role in affecting the propagation and refraction of light.

3-N-butylthiophene, with a purity of more than 98%, has relatively stable chemical properties. In this substance, the structure of the thiophene ring endows it with a certain aromaticity, and the introduction of butyl modifies its physical and chemical properties.
In terms of structural stability, the thiophene ring has a conjugated system, and the electron cloud is evenly distributed, which makes the entire molecular structure relatively stable. Under general chemical reaction conditions, without specific activation conditions, the thiophene ring is not prone to violent reactions such as ring opening. As an alkyl substituent, butyl is connected to the thiophene ring through the sigma-bond, which has a certain electron-donor induction effect. Although the electron cloud distribution of the thiophene ring is fine-tuned, the overall aromatic stability is maintained.
In terms of chemical stability, under conventional temperature, light and humidity environments, 3-N-butylthiophene can maintain a relatively stable state, and is not prone to common modification reactions such as automatic oxidation and hydrolysis. However, under extreme conditions such as high temperature, strong oxidants or strong acids and bases, its stability will be challenged. For example, when exposed to strong oxidants, the sulfur atoms on the thiophene ring may be oxidized, changing the molecular structure and properties; in a strong acid environment, the thiophene ring may undergo reactions such as protonation, which affect its chemical stability.
However, under normal storage and use conditions, due to its structural characteristics and high purity, the substance can maintain a relatively stable chemical properties for a certain period of time, providing a reliable material basis for related scientific research and industrial applications.

3-N-butylthiophene, with a content of more than 98%, the method of storage is related to the characteristics and safety of this substance, and it should be treated with care.
This chemical substance is more active, and may have certain volatility and chemical activity. When storing, the first priority is to choose a cool and well-ventilated place. Because if it is exposed to high temperature, its volatilization intensifies, not only the material is lost, but also the concentration accumulates, causing safety hazards, such as flammable, explosive and other risks. A cool environment can slow down its volatilization rate and maintain its chemical stability.
Furthermore, the storage place must be kept dry. If 3-N-butylthiophene encounters water vapor, or initiates chemical reactions such as hydrolysis, it will deteriorate and damage its quality. Therefore, it should be avoided in a humid place. A desiccant can be placed near the storage container to absorb the surrounding water vapor.
The choice of storage container is also crucial. When using corrosion-resistant materials, such as glass, specific plastics or metal materials. Glass containers are chemically stable and can be seen from the state of the material; however, some glasses may react with specific chemical substances, so be careful when using them. Plastic containers are lightweight and partially chemically resistant, but they should be prevented from swelling or penetrating. Metal containers are strong, so it is necessary to prevent them from reacting catalytically with materials by metal ions.
At the same time, the storage place should be kept away from fire sources, heat sources and oxidants. This substance is flammable, and in case of open flames and hot topics, it is easy to catch fire and burn, or even explode; and the oxidant comes into contact with it, or triggers a violent oxidation reaction, endangering safety.
In addition, the storage place should be clearly marked, indicating the name, content, storage date and other key information of 3-N-butylthiophene. This is for traceability and management, and to prevent misuse. And it is necessary to regularly check the storage status to see if it has any leakage or deterioration. If there is any abnormality, take countermeasures as soon as possible. Only in this way can 3-N-butylthiophene be properly stored to ensure its quality and storage safety.