Pyridine 4 Carboxaldoxime
pyridine pyrrole pyrazine piperidine piperazine

pyridine-4-carboxaldoxime

    Specifications

    HS Code

    314528

    Name pyridine-4-carboxaldoxime
    Molecular Formula C6H6N2O
    Molar Mass 122.124 g/mol
    Appearance White to off - white solid
    Melting Point 146 - 148 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, methanol, dichloromethane
    Odor Weak, characteristic odor
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    Frequently Asked Questions

    As a leading pyridine-4-carboxaldoxime supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of pyridine-4-carboxaldoxime?
    The chemical structure of pyridine-4-formaldehyde oxime is quite delicate. This is a unique class of organic compounds that builds its structure around the pyridine ring. The pyridine ring, like a stable "cornerstone", is cleverly connected by six atoms, in the shape of hexagons, and has aromatic properties, which is the key to giving the compound its unique chemical properties.
    At the fourth position of the pyridine ring, the aldoxime group is cleverly connected. The aldoxime group is the part formed by the condensation of the aldehyde group and the hydroxylamine. The aldehyde is basically active and can participate in many chemical reactions. After combining with hydroxylamine to synthesize oxime, it adds new properties. In the aldoxime structure, nitrogen atoms and oxygen atoms are arranged in a specific way to form a unique electron cloud distribution, which makes the entire pyridine-4-formaldehyde oxime molecule exhibit special reactivity and physical properties.
    From the perspective of spatial structure, the planarity of the pyridine ring and the spatial orientation of the aldoxime group affect each other, or affect the intermolecular forces, which in turn affect its performance in crystal structure, solubility, etc. Such a chemical structure is of great significance in the fields of organic synthesis, pharmaceutical chemistry, etc. It can be used as a key intermediate to participate in the construction of various complex compounds, providing a cornerstone for the exploration of new drugs and new materials.
    What are the main uses of pyridine-4-carboxaldoxime?
    Pyridine-4-carboxyaldoxime has a wide range of uses and is used in the fields of chemical industry and medicine.
    In the chemical industry, it is often a key raw material for organic synthesis. It can be used to build complex organic molecules with its special chemical structure. According to the principle of organic reaction, its aldehyde-oxime structure can participate in a variety of condensation and cyclization reactions, and then prepare other fine chemicals. For example, condensation with specific amines can produce nitrogen-containing heterocyclic compounds with specific functions. This is often an important step in the synthesis of dyes and fragrances.
    In the field of medicine, pyridine-4-carboxyaldoxime also has its work. First, it can be used as a pharmaceutical intermediate, through a series of chemical modifications, to make biologically active drugs. Second, studies have found that some of its derivatives may have specific pharmacological activities, such as antibacterial, anti-inflammatory, etc. From a pharmacological perspective, its structure may be compatible with the target in the organism, which can regulate the physiological process in the organism and achieve the purpose of treating diseases.
    In summary, pyridine-4-carboxyaldoxime plays a significant role in the chemical and pharmaceutical fields, and is the cornerstone of many chemical reactions and drug preparation. With the advance of science and technology, its use may become more extensive.
    What are the physical properties of pyridine-4-carboxaldoxime?
    Pyridine-4-carboxaldoxime (pyridine-4-carboxaldoxime) is an organic compound with unique physical properties. It is usually in the form of a white to pale yellow crystalline powder. In appearance, it has a regular shape and a fine texture.
    Its melting point has a clear range, generally in a specific temperature range, which makes the melting point determination a key method when identifying and purifying the substance. The solubility of pyridine-4-carboxaldoxime in water is limited, but it exhibits good solubility in some organic solvents, such as ethanol and dichloromethane. This solubility property provides a basis for its application in different chemical processes. For example, in some organic synthesis reactions, the appropriate solvent system can be selected according to this characteristic to promote the smooth progress of the reaction.
    Furthermore, pyridine-4-formaldehyde oxime has certain stability, but its structure will change under specific conditions, such as high temperature, strong acid or strong alkali environment. This requires that when storing and using the substance, the environmental conditions must be strictly controlled to ensure its stability. In addition, it also has a specific odor, although not strong and pungent, it is also unique. This odor can also be used as an auxiliary way to identify the substance in some scenarios. In conclusion, many physical properties of pyridine-4-formaldehyde oxime play a crucial role in its application in chemistry, medicine and other fields.
    What are pyridine-4-carboxaldoxime synthesis methods?
    There are many different methods for the synthesis of pyridine-4-formylaldoxime. The first method begins with pyridine-4-formaldehyde and reacts with hydroxylamine hydrochloride. The two are catalyzed by adding a base, such as sodium acetate, to a suitable solvent, such as ethanol. The appropriate temperature is about the degree of heating and reflux, which takes several hours. After this reaction, pyridine-4-formaldehyde is combined with hydroxylamine hydrochloride to form pyridine-4-formylaldoxime. After the reaction is completed, the solution is cooled, the product is precipitated in it, and then obtained by filtration, and then recrystallized with an appropriate solvent, such as a mixture of ethanol and water, to purify it.
    There is another method, using pyridine-4-formic acid as the initial material, first converted into its acid chloride. In response to thionyl chloride, in the environment of heating, the acid chloride is formed. Second, this acid chloride reacts with salts of hydroxylamines, such as hydroxylamine hydrochloride, in the environment of alkali. The base can be selected from triethylamine or the like, and the solvent can be selected from inert ones such as dichloromethane. In the reaction, the acid chloride interacts with the hydroxylamine salt to gradually form pyridine-4-formylaldoxime. Finally, after extraction, drying, vacuum distillation, etc., the pure product is obtained.
    There is another method, using pyridine-4-methylpyridine as the starting material, through oxidation to form pyridine-4-formaldehyde. This oxidizing agent can be selected as a mild manganese dioxide-sulfuric acid system. After that, pyridine-4-formaldehyde is obtained by reacting with hydroxylamine hydrochloride according to the first method, and pyridine-4-formylaldoxime can also be obtained.
    All kinds of synthesis methods have their own advantages and disadvantages, depending on the availability of raw materials, the level of cost, the difficulty of reaction and the purity of the product, etc., and choose the one that is suitable for use.
    pyridine-4-carboxaldoxime what are the precautions during use
    Pyridine-4-formaldehyde oxime is an important organic compound. During use, many precautions must be paid attention to.
    First safety protection. This compound has certain toxicity and irritation. When handling, be sure to wear suitable protective equipment, such as gloves, protective glasses and laboratory clothes, to avoid skin contact and eye splashing. If inadvertently exposed, rinse immediately with plenty of water and seek medical treatment according to specific conditions.
    Furthermore, pay attention to its chemical properties. Pyridine-4-formaldehyde oxime has specific chemical activity and is prone to react with a variety of substances. When storing, it should be placed in a dry, cool and well-ventilated place, away from fire sources, heat sources and strong oxidants, etc., to prevent dangerous reactions. During use, strictly follow the operating procedures and control the reaction conditions, such as temperature, pH, etc., to ensure that the reaction proceeds as expected and avoid accidents.
    In addition, the use environment should not be ignored. The operation should be carried out in a fume hood to effectively discharge volatile gases and prevent the accumulation of harmful gases, endangering personal health. At the same time, do a good job of waste disposal. This compound waste cannot be discarded at will. It should be properly disposed of in accordance with relevant regulations to prevent environmental pollution.
    In conclusion, when using pyridine-4-formaldehyde oxime, safety awareness is indispensable, careful operation, and strict compliance with regulations can ensure the safety and smoothness of the use process.