4 Amino Pyrazine
pyridine pyrrole pyrazine piperidine piperazine

4-amino-pyrazine

    Specifications

    HS Code

    285311

    Chemical Formula C4H5N3
    Molar Mass 95.10 g/mol
    Appearance Solid
    Melting Point 137 - 140 °C
    Boiling Point 326.8 °C at 760 mmHg
    Solubility In Water Soluble
    Odor Characteristic
    Density 1.29 g/cm³
    Flash Point 151.4 °C
    Pka 4.26

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    Frequently Asked Questions

    As a leading 4-amino-pyrazine 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 4-aminopyrazine?
    4-Hydroxypyridine is an organic compound with unique physical properties. Looking at its morphology, under room temperature and pressure, 4-Hydroxypyridine is mostly in the state of white to light yellow crystalline powder, which is easy to store and use, and also reflects the order of its molecular arrangement.
    When it comes to melting point, 4-Hydroxypyridine has a high melting point, about 145-148 ° C. This higher melting point is due to the interaction forces such as hydrogen bonds between molecules, which make the molecules closely connected, requiring more energy to destroy the lattice and realize the transition from solid to liquid.
    In terms of solubility, 4-Hydroxypyridine is soluble in common solvents such as water, ethanol, and ether. In water, it forms hydrogen bonds with hydroxyl groups and water molecules to enhance the interaction between molecules and water molecules, so it has a certain solubility. In organic solvents, the van der Waals force between its molecules and solvent molecules also makes it well soluble. This property provides convenient conditions for its participation in reactions in organic synthesis and other fields.
    4-hydroxypyridine has sublimation properties, and can be directly converted from solid to gaseous state under specific temperature and pressure conditions. This property has potential application value in material purification. It can be separated from impurities through sublimation operations to obtain high-purity 4-hydroxypyridine.
    In addition, when 4-hydroxypyridine is in the solid state, the molecule forms an ordered crystal structure through hydrogen bonding and other actions, giving it certain crystal characteristics. In the liquid or solution state, the molecular movement is more free, but it is still affected by intermolecular forces. The diversity of its physical properties lays the foundation for chemical research and practical applications. Whether it is used as an intermediate in organic synthesis or in drug development, it shows important value due to its unique physical properties.
    What are the chemical properties of 4-aminopyrazine?
    4-Hydroxypyridine is an organic compound with many unique chemical properties.
    In terms of acidity and alkalinity, 4-Hydroxypyridine is both acidic and basic. Due to the high electronegativity of oxygen atoms in the hydroxyl group, the hydroxyhydrogen atoms are easily dissociated in the form of protons, showing a certain acidity; at the same time, the nitrogen atoms in the pyridine ring have lone pairs of electrons and can accept protons, so they are also alkaline. This amphoteric property makes 4-Hydroxypyridine capable of acting as both acid and base in specific chemical reactions.
    The nucleophilicity and electrophilicity of 4-Hydroxypyridine cannot be ignored. Due to the presence of nitrogen atoms, the electron cloud density distribution of the pyridine ring is uneven, and the electron cloud density of the adjacent and para-position of the nitrogen atom is relatively low, showing electrophilicity; while the hydroxyl oxygen atom is rich in lone pair electrons and has nucleophilicity. In the nucleophilic substitution reaction, the lone pair electrons of the hydroxyl oxygen atom can attack the electrophilic reagent; in the electrophilic substitution reaction, the pyridine ring becomes the target of the electrophilic reagent attack.
    4-hydroxypyridine also has a certain coordination ability. With the lone pair electrons of the hydroxyl oxygen atom and the nitrogen atom of the pyridine ring, it can form coordination bonds with metal ions to form metal complexes. Such metal complexes are widely used in catalysis, materials science and other fields, such as as catalysts to accelerate the process of certain chemical reactions.
    In addition, 4-hydroxypyridine can form intramolecular or intermolecular hydrogen bonds due to the presence of hydroxyl and pyridine rings in the molecule. The formation of hydrogen bonds has a significant impact on its physical properties, such as melting point, boiling point, solubility, etc., and also affects its aggregation state and reactivity in solution.
    In summary, these chemical properties of 4-hydroxypyridine make it have important applications and research values in many fields such as organic synthesis, medicinal chemistry, and materials science.
    What fields are 4-aminopyrazine used in?
    4-Hydroxyacetophenone has its uses in various fields. In the field of medicine, it is an important raw material of traditional Chinese medicine. It can be used to make antibacterial and antiviral drugs. Because of its specific chemical structure, it can interact with the biomacromolecules of pathogens and prevent their growth and reproduction. For example, some drugs for the treatment of respiratory infections, 4-Hydroxyacetophenone is a key link in the synthesis process, helping to improve the efficacy of drugs.
    In the fragrance industry, 4-Hydroxyacetophenone is also highly valued. It has a unique aroma and can add a unique flavor to fragrance formulations. It can be used to prepare floral and fruity fragrances to increase the layering and richness of fragrances. In daily chemicals, such as perfumes and air fresheners, 4-hydroxyacetophenone can make the aroma more lasting and pleasant.
    Furthermore, in the chemical industry, it is an important intermediate for the synthesis of many fine chemicals. After a series of chemical reactions, materials and compounds with different functions can be prepared. In organic synthesis reactions, the hydroxyl and ketone groups of 4-hydroxyacetophenone can participate in many reactions, such as esterification, condensation, etc., resulting in multiple products to meet the diverse needs of the chemical industry.
    In the field of food additives, 4-hydroxyacetophenone can be used as a flavoring agent. Because of its special smell, it can improve the flavor of food and increase the attractiveness of food. In baked goods and beverages, appropriate addition can give a unique aroma and improve the quality of food.
    It can be seen that 4-hydroxyacetophenone plays an important role in the fields of medicine, flavors, chemicals, food, etc. With its unique chemical properties, it has made great contributions to the development of various industries.
    What are the synthesis methods of 4-aminopyrazine?
    4-Hydroxypyridine is an important intermediate in organic synthesis. Its synthesis methods are diverse, and many researchers have studied it through the ages. The following are common methods:
    First, the method of using pyridine as the starting material. Under specific conditions, pyridine reacts with strong oxidants such as peroxyacid, and the pyridine ring is oxidized to form pyridine N-oxide. Pyridine N-oxide reacts with nucleophiles, and the nucleophiles attack specific positions on the pyridine ring. After a series of reactions, 4-hydroxypyridine is finally formed. The starting material pyridine for this route is easy to obtain, but the reaction steps are slightly complicated, and the reaction conditions need to be carefully controlled to improve the yield and purity.
    Second, it is prepared by 4-halopyridine. 4-halopyridine (such as 4-chloropyridine, 4-bromopyridine, etc.) reacts with nucleophiles (such as sodium hydroxide aqueous solution, sodium alcohol, etc.) in an appropriate solvent by heating, and the halogen atom is replaced by hydroxyl to generate 4-hydroxypyridine. This method is relatively direct, and the key lies in the preparation and acquisition of 4-halopyridine, and the activity of halopyridine needs to be fully considered to ensure the smooth progress of the substitution reaction.
    Third, the cyclization reaction is used to construct. Using suitable chain compounds as raw materials, pyridine rings are formed through intra-molecular ring-closing reactions, and hydroxyl groups are introduced to generate 4-hydroxypyridine. For example, some chain compounds containing nitrogen, oxygen and unsaturated bonds can be cyclized within the molecule under conditions such as catalyst and heating to generate the target product. This approach is cleverly designed, requires precise design of the raw material structure, and also has high requirements on the reaction conditions to guide the reaction to the desired cyclization direction.
    Fourth, biosynthesis. With the help of microorganisms or enzymes, 4-hydroxypyridine is synthesized in a specific biological metabolic pathway. Some microorganisms can use simple carbon and nitrogen sources to generate 4-hydroxypyridine and its analogs through complex enzyme catalysis in the body during the metabolic process. Biosynthesis has the advantages of green and mild, but it is currently limited by the complexity and controllability of biological systems, and industrial applications still need to be further studied.
    What is the market prospect of 4-aminopyrazine?
    4-Hydroxyacetophenone has considerable market prospects in this world. This product has a wide range of uses, so the market demand is on the rise.
    In the field of medicine, 4-hydroxyacetophenone is a key intermediate for many drugs. Due to its special chemical structure, it can be used to synthesize a variety of drugs with therapeutic effects. In today's world, people are increasingly concerned about health, the pharmaceutical industry is booming, and the demand for various drugs is also rising. This creates a broad space for 4-hydroxyacetophenone in the pharmaceutical intermediate market. Many pharmaceutical companies are actively seeking high-quality 4-hydroxyacetophenone to meet their drug development and production needs.
    In the fragrance industry, 4-hydroxyacetophenone also has outstanding performance. Its unique aroma can add a different flavor to the fragrance. With the improvement of people's quality of life, the demand for fragrance products such as perfumes and cosmetics is increasingly diverse. 4-hydroxyacetophenone is often used to prepare various high-end fragrances to meet consumers' pursuit of unique fragrances due to its unique aroma characteristics. Therefore, the demand for 4-hydroxyacetophenone in the fragrance industry also continues to grow.
    Furthermore, in the chemical industry, 4-hydroxyacetophenone can be used as an important raw material for organic synthesis. With the continuous progress of the chemical industry, the demand for various high-performance chemical raw materials is also increasing. 4-Hydroxyacetophenone plays an important role in chemical synthesis due to its excellent chemical properties, and many chemical companies have increased their procurement and application efforts.
    However, although the market prospect is good, there are also challenges. The optimization and improvement of production technology is a top priority for enterprises. To meet the growing demand of the market, it is necessary to improve production efficiency and reduce production costs. And environmental protection requirements are becoming stricter, and green environmental protection needs to be paid attention to in the production process to meet the requirements of regulations.
    In general, the market prospect of 4-hydroxyacetophenone is bright, and there is considerable demand in many fields such as medicine, fragrance, and chemical industry. However, enterprises need to deal with challenges such as production technology and environmental protection in order to occupy a favorable position in market competition.