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1-ethyl-1H-pyrrole-2, what is the chemical structure of 5-dione?
1 - ethyl - 1H - pyrrole - 2,5 - dione, which is also a kind of thing. Its transformation is made up of a pyrrole. Pyrrole, which contains five-element nitrogen, has a total of four carbon atoms and one nitrogen atom. In the first position of pyrrole, there is an ethyl group, which is formed from one carbon atom and three carbon atoms on the nitrogen atom of pyrrole. And in the second position and the fifth position of pyrrole, there is a carbonyl group. The carbonyl group is a functional group composed of one carbon atom and one oxygen atom. Therefore, the integration of 1 - ethyl - 1H - pyrrole - 2,5 - dione is based on pyrrole, 1 has ethyl repair, and 2 has 5 have a carbonyl connection, which shows a specific transformation image. This gives it a specific transformation property, so that it can exhibit a specific role in the reaction and transformation domains.
1-ethyl-1H-pyrrole-2, what are the main uses of 5-dione
1 - ethyl - 1H - pyrrole - 2,5 - dione, the Chinese name of 1 - ethyl - 1H - pyrrole - 2,5 - dione, its main use.
First, in the field of synthesis, this is the most important raw material. It can be synthesized by general reaction, such as nuclear substitution, addition, etc., and various kinds of chemical compounds. Its molecules contain special functionalities and can be enriched to obtain compounds with specific chemical functions. For example, it is used in the synthesis of materials with special light and chemical properties, or in materials with specific biological activities.
Second, in terms of materials science, it can be synthesized into polymers. The copolymerization of other polymers can improve the properties of polymers, such as improving their mechanical strength, resistance, solubility, etc. The obtained polymer materials can be used to create high-performance engineering plastics, which can be used in aerospace, steam and other materials with strict performance requirements; or can be used as special materials to ensure good performance of the coating.
Third, in the field of material research, its biological activity is affected. Some of the compounds based on 1-ethyl-1H-pyrrole-2,5-dione are studied to have antibacterial, anti-inflammatory, anti-cancer and other biological activities. The scientific research team uses the mother nucleus to synthesize a series of derivatives, resulting in better activity and lower toxicity, providing an important direction for new research.
Fourth, it also has a place in the dye industry. Because it can derive compounds with specific color and light quality, it can be used as a dye for printing, printing and other industries, so that the material or printed matter has a long-lasting color.
1-ethyl-1H-pyrrole-2, what are the physical properties of 5-dione
1 - ethyl - 1H - pyrrole - 2,5 - dione, the Chinese name is often called N - ethylmaleimide. This substance has the following physical properties:
Viewed at room temperature, it is colorless to light yellow liquid, its quality is clear and its visibility is good. Smell, there is a pungent smell that is pungent and uncomfortable to smell. This smell can spread rapidly in the air and is easily detectable by people.
Its melting point is about -21 ° C. At this temperature, the substance gradually changes from liquid to solid, and the molecular movement slows down and the arrangement tends to be orderly. The boiling point is at 215-218 ° C. When the temperature rises to the boiling point, the liquid vaporizes violently, and the molecules can break free from the shackles of the liquid phase and escape into the gas phase.
N-ethylmaleimide has a density of about 1.104 g/cm ³, which is slightly heavier than water. If mixed with water, it sinks underwater. In terms of solubility, it can be soluble in a variety of organic solvents, such as ethanol, ether, acetone, etc., which can be uniformly dispersed and interact with organic solvent molecules to form a uniform system; however, its solubility in water is limited. Due to its molecular structure characteristics, the force between water molecules is weak, and it is difficult to miscible with water.
In addition, N-ethylmaleimide is volatile. In the air, its molecules constantly move and escape from the liquid surface, causing its concentration in the air to gradually change. Because of its irritation, it evaporates in the air and can cause irritation to the human respiratory tract, eyes, and other parts.
1-ethyl-1H-pyrrole-2, what is the preparation method of 5-dione
1-Ethyl-1H-pyrrole-2,5-dione is 1-ethyl-1H-pyrrole-2,5-dione, also known as N-ethylmaleimide. The preparation method is as follows:
To prepare 1-ethyl-1H-pyrrole-2,5-dione, maleic anhydride and ethylamine are often used as starting materials. First take an appropriate amount of maleic anhydride and place it in a suitable reaction vessel. This maleic anhydride, if white crystalline and active in nature, is the key substrate for the reaction.
Then, ethylamine is slowly added dropwise to a container containing maleic anhydride. Ethylamine has a pungent odor and is chemically active. When adding dropwise, care should be taken to control the dropwise rate to prevent the reaction from being too violent. When the two meet, an aminolysis reaction occurs first, and the amino group of ethylamine attacks the carbonyl carbon of maleic anhydride to form an intermediate product. During this process, the temperature of the system may change, and appropriate means must be used to regulate the temperature to make the reaction proceed smoothly.
After a period of reaction, the intermediate product is dehydrated and cyclized in the molecule to obtain 1-ethyl-1H-pyrrole-2,5-dione. In order to complete the reaction, it is often necessary to heat and maintain for a certain period of time to promote the full occurrence of dehydration cyclization.
After the reaction is completed, the product may contain impurities such as unreacted raw materials and by-products. Purification can be obtained by means of distillation and recrystallization. During distillation, the target product is separated according to the difference in the boiling point of each component. Recrystallization is to use the different solubility of the product and impurities in a specific solvent to obtain a pure 1-ethyl-1H-pyrrole-2,5-dione. In this way, a purer target product can be obtained.
1-ethyl-1H-pyrrole-2, what are the precautions in the use of 5-dione
1-Ethyl-1H-pyrrole-2,5-dione is 1-ethyl-1H-pyrrole-2,5-dione, also known as N-ethylmaleimide. When using, pay attention to the following things:
First, this product has certain toxicity and irritation, and can cause discomfort if it touches the skin, eyes or inhales its vapors. When operating, be sure to wear appropriate protective equipment, such as gloves, goggles and masks, to prevent direct contact with it. In case of accidental contact, rinse with plenty of water immediately and seek medical attention according to the specific situation.
Second, 1-ethyl-1H-pyrrole-2,5-dione has active chemical properties and is easy to react with many compounds under specific conditions. When storing, it should be placed in a dry, cool and well-ventilated place, away from fire, heat and oxidants, etc., to prevent dangerous reactions. Before use, it is also necessary to carefully check its chemical properties and reaction characteristics to ensure that the operating environment and conditions are suitable to avoid safety accidents caused by uncontrolled reactions.
Third, during the weighing and transfer of the substance, it is necessary to operate with precision. Due to its high reactivity, the amount may have a significant impact on the reaction results. After taking it, the container should be sealed in time to prevent it from deteriorating in contact with air, moisture and other substances.
Fourth, after use, the waste containing 1-ethyl-1H-pyrrole-2,5-dione should be properly disposed of in accordance with relevant regulations. Do not dump it at will to avoid polluting the environment. According to its chemical properties, use appropriate methods for harmless treatment or recycling.