Pyrazine 2 3 Diethyl 5 Methyl
pyridine pyrrole pyrazine piperidine piperazine

pyrazine, 2,3-diethyl-5-methyl-

    Specifications

    HS Code

    473702

    Name pyrazine, 2,3 - diethyl - 5 - methyl -
    Molecular Formula C9H14N2
    Molar Mass 150.22 g/mol
    Appearance Unknown (no common default appearance data for this specific compound)
    Boiling Point Unknown (no common default data for this specific compound)
    Melting Point Unknown (no common default data for this specific compound)
    Solubility In Water Unknown (no common default data for this specific compound)
    Density Unknown (no common default data for this specific compound)
    Vapor Pressure Unknown (no common default data for this specific compound)
    Flash Point Unknown (no common default data for this specific compound)

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of pyrazine, 2,3-diethyl-5-methyl-?
    This is a difficult problem in organic chemistry. The chemical structure of the compound referred to in "pyrazine, 2,3-diethyl-5-methyl -" is investigated as follows.
    The first concept of "pyrazine" is pyrazine, which is a hexadecyclic compound containing two nitrogen atoms. Its ring has a conjugated system and is quite stable. The structure of pyrazine is like a hexagonal ring, with two nitrogen atoms intersected on the ring.
    Next, "2,3-diethyl -" is said to be in the 2nd and 3rd positions of the pyrazine ring, each connected with an ethyl group ($- C_ {2} H_ {5} $). Ethyl, an alkyl group composed of two carbon atoms and five hydrogen atoms, which is in the shape of a chain and connected to a specific position of the pyrazine ring.
    Looking at "5-methyl -" again, it means that at the 5th position of the pyrazine ring, there is a methyl group ($- CH_ {3} $). The methyl group contains only one carbon atom and three hydrogen atoms, and is also connected to the corresponding check point of the pyrazine ring.
    In summary, the structure of this compound is based on the pyrazine ring as the parent nucleus, with one ethyl group at the 2nd and 3rd positions, and one methyl group at the 5th position. In this way, the chemical structure of "pyrazine, 2,3 - diethyl - 5 - methyl -" is obtained. The analysis of this structure requires a thorough understanding of the naming rules of organic chemistry and the characteristics of various groups in order to be correct.
    What are the physical properties of pyrazine, 2,3-diethyl-5-methyl-
    "Tiangong Kaiwu" is the treasure of ancient science and technology in our country, but now I am asking "pyrazine, 2,3-diethyl-5-methyl -" This thing is an organic matter named by modern chemistry, named 2,3-diethyl-5-methyl pyrazine, which is not known in the era of "Tiangong Kaiwu". I will describe its physical properties in modern chemical knowledge and ancient words.
    This 2,3-diethyl-5-methyl pyrazine is mostly liquid under normal conditions. When it is pure, it may be colorless and transparent, if it contains some impurities, or has a very light yellow. It has a special smell, like the aroma of baking mixed with nutty smell, subtle and unique, and is often used in the field of food flavoring to enhance flavor.
    In terms of its boiling point, it is about 190-200 ° C, which fluctuates slightly due to the difference in ambient air pressure. The boiling point is the critical temperature at which a substance changes from a liquid state to a gas state. At this temperature, the inside and surface of the liquid are violently vaporized at the same time. Its melting point is low, and it is usually at room temperature, showing a flowing liquid state. The melting point is the temperature at which a substance changes from a solid state to a liquid state.
    As for the density, it is slightly smaller than that of water, about 0.9-1.0 g/cm ³, so if mixed with water, it floats on water. In terms of solubility, it is slightly soluble in water, with fewer hydrophilic groups and more hydrophobic alkyl groups in its molecular structure. However, it is soluble in many organic solvents, such as ethanol, ether, etc. This is due to the principle of "similar phase dissolution". The structure of the organic solvent is similar to that of the organic substance, and the intermolecular forces are appropriate, so it is compatible.
    Its volatility is moderate, and it can slowly evaporate in the air, emitting a unique odor. And its vapor pressure has a certain value at room temperature. For the vapor pressure, when the gaseous state and the liquid state of the substance are in equilibrium, the pressure of the gaseous state is related to its volatility.
    What are the chemical properties of pyrazine, 2,3-diethyl-5-methyl-
    2,3-Diethyl-5-methylpyrazine is an organic compound with unique chemical properties and is useful in many fields.
    This compound is volatile and may emit a special odor at room temperature. Its odor is often described as having roasted, nutty or popcorn-like aroma, which makes it widely used in the field of food flavoring. It can be used as a flavoring agent to impart unique flavors to various foods, such as baked goods, nut products, etc., to enhance the aroma level and richness of food, making it more attractive.
    From the perspective of chemical structure, the pyrazine ring is its core structure, and the diethyl and methyl groups connected to the ring have a great impact on its properties. The presence of these alkyl groups alters molecular polarity and steric resistance, affecting the solubility of compounds. Relatively speaking, its solubility in organic solvents may be better than in water, which is conducive to its separation, purification and reaction operation in organic synthesis and industrial production processes.
    In chemical reactions, hydrogen atoms on the 2,3-diethyl-5-methylpyrazine ring have certain activity and can participate in various substitution reactions. For example, under appropriate conditions, electrophilic substitution reactions can occur with electrophilic reagents, introducing new functional groups, and then synthesizing compounds with more complex structures for the preparation of pharmaceutical intermediates or other fine chemicals.
    Due to its unique chemical structure and properties, 2,3-diethyl-5-methylpyrazine occupies an important position in many fields such as fragrance preparation, organic synthesis and food industry. With the deepening of research and technological development, its application prospect may be broader.
    What are the main uses of pyrazine, 2,3-diethyl-5-methyl-?
    Pyrazine, 2,3-diethyl-5-methyl, is used in many fields. In the field of medicine, it is often the key raw material for the creation of new medicines. Doctors use its chemical characteristics to carefully develop and prepare it, hoping that it can become a cure for diseases, or an antibacterial agent to control the invasion of pathogens; or a medicine for regulating the body, so that the functions of the viscera can be restored.
    In the world of fragrances, it also has extraordinary performance. Fragrances use its unique smell skillfully, either quiet and elegant, or rich and charming, integrated into various fragrance formulas. It can add a mysterious charm to the perfume, making the user linger with a unique fragrance, as if in a dreamland; it can also add a different flavor to the food, making cakes, candies and other delicacies more tempting, and arousing diners.
    In the chemical industry, as an important chemical raw material, it participates in many synthetic reactions. Chemical craftsmen use it to participate in complex chemical processes to produce various chemical products such as high-performance plastics and high-quality fibers, which are widely used in the manufacture of various objects in life, bringing convenience and quality improvement to people's lives.
    In the path of scientific research and exploration, pyrazine, 2,3-diethyl-5-methyl, is also a weapon in the hands of researchers. To help them delve deeper into the mechanism of chemical reactions, gain insight into the mysteries of the microscopic world, and contribute to the development of chemistry, thus promoting the continuous advancement of science and technology.
    What are the preparation methods of pyrazine, 2,3-diethyl-5-methyl-
    To prepare 2,3-diethyl-5-methylpyrazine, there are many methods, and the main ones are selected.
    First, it can be obtained from the condensation reaction of the corresponding aldehyde and amine compounds. First, take an appropriate amount of aldehyde and amine, put them in a clean container, and dissolve them in a specific organic solvent. This organic solvent must have good solubility and no side reactions with the reactants. Add an appropriate amount of catalyst. The choice of catalyst is related to the reaction rate and yield, usually acid or alkali catalysts. Under suitable temperature and pressure, stir the reaction. The temperature control is very important. If it is too high, side reactions will occur frequently, and if it is too low, the reaction will be slow. After a certain period of time, the desired crude product of 2,3-diethyl-5-methylpyrazine can be obtained, and then purified by distillation, recrystallization, etc. to remove its impurities and obtain a pure product.
    Second, compounds containing specific groups can also be prepared by intramolecular cyclization. First, chain compounds containing appropriate substituents are heated under specific reaction conditions, such as metal salts as catalysts, in an inert gas protective atmosphere. Metal salt catalysts can effectively promote intramolecular cyclization, and inert gases can prevent oxidation of reactants. After the reaction is completed, the mixture of products is obtained, and then 2,3-diethyl-5-methylpyrazine is separated by chromatographic separation and other means.
    Third, there is still a way to use natural products as starting materials. Some natural plant or microbial metabolites contain ingredients that can be converted into target products. First, the relevant ingredients are extracted from natural resources. This process may require multiple steps such as extraction and filtration. After the extracted ingredients are chemically modified, and after several steps of reaction, the target molecular structure is gradually constructed, and finally 2,3-diethyl-5-methylpyrazine is obtained.
    The above methods have their own advantages and disadvantages. In actual preparation, they should be selected according to factors such as raw material availability, cost, and product purity requirements.