2 Aminopyrazine Aminopyrazine
pyridine pyrrole pyrazine piperidine piperazine

2-aminopyrazine Aminopyrazine

    Specifications

    HS Code

    209776

    Name 2-aminopyrazine
    Molecular Formula C4H5N3
    Molecular Weight 95.10 g/mol
    Appearance Pale yellow to light brown solid
    Melting Point 90 - 93 °C
    Boiling Point 254 - 255 °C
    Solubility Soluble in water, ethanol, ether
    Density 1.24 g/cm³
    Pka 3.79
    Flash Point 115 °C
    Cas Number 139-12-8

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    General Information
    Where to Buy 2-aminopyrazine Aminopyrazine in China?
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    Frequently Asked Questions

    As a leading 2-aminopyrazine Aminopyrazine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the physical properties of 2-aminopyrazine?
    2-%E6%B0%A8%E5%9F%BA%E5%90%A1%E5%97%AA, its color is white and crystalline, often in the state of powder. This material has a specific smell, although not pungent and intolerable, it is also unique, and its unique smell can be distinguished by the smell.
    In terms of its melting and boiling point, the melting point is about [specific value] ℃. When heated to this temperature, the 2-%E6%B0%A8%E5%9F%BA%E5%90%A1%E5%97%AA gradually melts from the solid state into a liquid state, and the process is smooth and orderly. The boiling point is about [specific value] ℃. Under a specific pressure environment, it turns into gaseous ascension when it reaches this temperature.
    Its solubility is also an important physical property. In water, 2-%E6%B0%A8%E5%9F%BA%E5%90%A1%E5%97%AA has a certain solubility. Although it is not very soluble, it can be partially dissolved in water when appropriate, forming a uniform mixed system. In organic solvents, such as ethanol and acetone, its solubility is better, and it can be well miscible with solvents, which makes it useful in many organic synthesis reactions and related experimental operations.
    As for the density, 2-%E6%B0%A8%E5%9F%BA%E5%90%A1%E5%97%AA is different from common solvents, about [specific value] g/cm ³. This value determines its position and distribution in a specific system. It is one of the key considerations when involving experimental phenomena such as stratification and industrial production process design.
    In addition, the stability of light and heat 2-%E6%B0%A8%E5%9F%BA%E5%90%A1%E5%97%AA also needs to be paid attention to. In moderate light and normal temperature range, its properties are relatively stable, but if it is exposed to strong light for a long time or in a high temperature environment, its structure may change, which in turn affects its chemical activity and related applications.
    What are the chemical properties of 2-aminopyrazine?
    2-Aminopyrazine (2-aminopyrazine, Aminopyrazine) is an organic compound with unique chemical properties.
    It is basic, and the nitrogen atom in the guain amino group contains lone pairs of electrons, which can bind protons and form salts in acidic solutions. This property makes it act as a base in chemical reactions, neutralizing with acids.
    2-aminopyrazine is aromatic, the pyrazine ring conforms to the Shocker rule, has a closed conjugate system, and the number of π electrons is 6, which makes it stable. And the aromaticity has a great influence on its chemical properties. For example, in the electrophilic substitution reaction, the pyrazine ring can stabilize the reaction intermediate, which is conducive to the reaction. < Br >
    It can participate in the electrophilic substitution reaction. Because the amino group is the power supply group, the electron cloud density of the pyrazine ring will increase, especially the amino ortho and para-positions, and the electrophilic reagents are easy to attack these positions. Like halogenation, nitrification, sulfonation and other electrophilic substitution reactions, 2-aminopyrazine can occur.
    2-aminopyrazine can also participate in nucleophilic substitution reactions. When the pyrazine ring is connected with a suitable leaving group, the nucleophilic reagent can attack the pyrazine ring, leaving the leaving group and realizing nucleophilic substitution.
    In redox reactions, 2-aminopyrazine also exhibits. Amino groups can be oxidized, and pyrazine rings can also undergo oxidation reactions under specific conditions; at the same time, under the action of reducing agents, pyrazine rings can be reduced and hydrogenation reactions can occur.
    In addition, 2-amino pyrazines can form complexes with metal ions, and the lone pair electrons of amino nitrogen atoms can coordinate with metal ions to form stable complexes. This property may have applications in materials science, catalysis and other fields.
    What are the main applications of 2-aminopyrazine?
    2-Aminopyrazine has a wide range of uses and has its own impact in many fields.
    In the field of medicine, its importance cannot be underestimated. It is often a key intermediate in the synthesis of various drugs. The unique chemical structure of 2-aminopyrazine gives it the potential to interact with specific targets in organisms. With this, medicinal chemists can modify and modify its structure to create drugs for the treatment of various diseases, such as antibacterial drugs, which can effectively inhibit the growth and reproduction of bacteria and protect human health; and anticancer drugs, which are expected to play a role in the specific physiological mechanisms of cancer cells and help solve cancer problems.
    In the field of materials science, it also plays an important role. Often involved in the synthesis of functional materials. For example, in the preparation of organic optoelectronic materials, 2-aminopyrazine can be used as a construction unit to affect the photoelectric properties of the materials. After rational design and synthesis, materials containing 2-aminopyrazine may have excellent luminescence properties and can be applied to organic Light Emitting Diode (OLED) devices, contributing to the development of display technology; or have unique electrical properties, emerging in the field of semiconductor materials, promoting the miniaturization and efficiency of electronic devices.
    In the field of pesticides, it also plays a role. Or as a raw material for the synthesis of new pesticides. The synthetic pesticides may have the characteristics of high efficiency, low toxicity and environmental friendliness, which can not only effectively control crop diseases and pests, ensure food yield and quality, but also reduce the negative impact on the environment, and meet the needs of the current green agriculture development.
    In the field of fine chemicals, it is also a commonly used raw material. It is used to synthesize various fine chemicals, such as dyes, fragrances, etc. Taking dye synthesis as an example, 2-aminopyrazine can introduce a specific structure, endow dyes with unique colors and properties, and meet the diverse needs of different industries for dyes.
    In summary, 2-aminopyrazine occupies an important position in the fields of medicine, materials science, pesticides, and fine chemicals, and plays a positive role in promoting the development of various fields.
    What is the preparation method of 2-aminopyrazine?
    For 2-aminopyrazine, there are various ways to prepare it. One is to use pyrazine as a base to react with ammonia under suitable conditions. Among them, an appropriate catalyst, such as metal oxides, needs to be selected. In a high temperature and high pressure environment, the hydrogen atom on the ring of pyrazine is replaced by an amino group, so 2-aminopyrazine is obtained. In this process, the control of temperature is the key. If it is too high, side reactions will occur, and if it is too low, the reaction will be slow and the efficiency will be poor.
    The second method is to conduct a condensation reaction between a nitrogen-containing compound and a substance with active functional groups. For example, when a compound containing an amino group and a pyrazine derivative containing a halogen atom are catalyzed by a base, the halogen atom and the amino group undergo a nucleophilic substitution reaction. The strength of the base and the ratio of the reactants will affect the yield and purity of the reaction. Fine regulation is required to make the reaction proceed smoothly in the direction of generating 2-aminopyrazine.
    Furthermore, it can be obtained from other heterocyclic compounds through a series of conversions. First, the heterocyclic ring is opened or modified by a specific reaction, the amino-related group is introduced, and then the ring is closed to form the pyrazine ring and retain the amino group, so as to obtain 2-aminopyrazine. This path is more complicated, but it is also a feasible method under specific raw materials and conditions. In the process of preparation, separation and purification are also important, and impurities are often removed by recrystallization, column chromatography, etc., to obtain pure 2-aminopyrazine to meet the required quality.
    What is the market outlook for 2-aminopyrazine?
    2-Aminopyrazine is a key raw material and intermediate in the field of organic synthesis. It is widely used in many industries such as medicine, pesticides, dyes and materials.
    Looking at the pharmaceutical industry, with the increasing aging of the global population and the increasing emphasis on health, the research and development of various drugs continues to heat up. 2-Aminopyrazine, as an important intermediate, plays an indispensable role in the synthesis of antibacterial, antiviral, anti-tumor and other drugs. For example, the creation of some new antibacterial drugs relies on the unique chemical structure of 2-Aminopyrazine to enhance the effect of drugs on bacteria. Therefore, the demand for 2-Aminopyrazine in the pharmaceutical field is likely to rise steadily in the future.
    In the pesticide industry, in order to ensure the yield and quality of agricultural products, the demand for high-efficiency and low-toxicity pesticides is growing. 2-Aminopyrazine can be used to synthesize pesticides with unique mechanisms of action, such as some pesticides and fungicides that target specific pests or diseases. With the increasing awareness of environmental protection and the increasing attention to food safety, the development of green and environmentally friendly pesticides has become a trend. 2-Aminopyrazine, with its own characteristics, is expected to gain more application opportunities in the creation of new pesticides, and the market prospect is quite broad.
    In the dye industry, people are increasingly demanding on the color brightness, stability and environmental protection of dyes. 2-Aminopyrazine can endow dye molecules with special structures and properties, and help to develop high-quality dye products that meet environmental standards. With the development of textile, printing and dyeing industries, the demand for high-quality dyes will also promote the expansion of the 2-aminopyrazine market.
    In the field of materials, with the advancement of science and technology, the exploration of functional materials continues to deepen. 2-aminopyrazine can participate in the synthesis of materials with special optoelectronic properties and thermal stability, and may have potential applications in electronic devices, optical materials, etc. The rise of emerging materials industries will open up a new market space for 2-aminopyrazine.
    Overall, 2-aminopyrazine is widely used in many industries, accompanied by the continuous development and technological innovation of various industries. Its market prospect is relatively optimistic, and the demand is expected to gradually increase.