N Hydroxypyridine 2 Carboximidamide
pyridine pyrrole pyrazine piperidine piperazine

N'-HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE

    Specifications

    HS Code

    681207

    Chemical Formula C6H7N3O
    Molar Mass 137.14 g/mol
    Appearance Solid (presumably, based on common chemical properties)

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    General Information
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    Frequently Asked Questions

    As a leading N'-HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE 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 N -HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE?
    Alas! The chemical structure of "N '-hydroxypyridine-2-formamidine" is involved in the field of organic chemistry. Looking at its name, the pyridine ring is the base, and this ring has the structure of a six-membered aromatic heterocycle, which is cleverly connected by five carbon atoms and one nitrogen atom. It is planar and aromatic.
    At the second position of the pyridine ring, there is a formamidine group attached. Formamidine is a structural unit connected by a carbon-nitrogen double bond (C = N) and an amino group (-NH ²). And "N' -hydroxyl" is represented on the nitrogen atom of formamidine, connected with a hydroxyl group (-OH).
    In this structure, the pyridine ring endows it with certain stability and electron cloud distribution characteristics, and the formamidine group may participate in many reactions because of its active nitrogen atom and carbon-nitrogen double bond. The presence of hydroxyl groups adds hydrophilicity and reactivity, and can participate in the formation of hydrogen bonds, or substitution and dehydration reactions under appropriate conditions. Its overall structure makes the compound have unique properties and uses in the fields of organic synthesis, pharmaceutical chemistry, etc.
    What are the main uses of N -HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE?
    The use of N '-hydroxypyridine-2-formamidine is quite critical and has applications in many fields.
    First, in the process of pharmaceutical research and development, this compound has a significant effect. It can be used as a lead compound for medical scientists to explore in depth. Because it has a specific chemical structure and activity, it may have an impact on specific physiological mechanisms of the human body. For example, after modification and optimization, it can be used to develop antibacterial drugs. Its structural properties may interfere with the synthesis and metabolic pathways of bacterial cell walls, etc., so as to inhibit or kill bacteria, providing new possibilities for dealing with bacterial infections.
    Second, it also has potential applications in the field of materials science. Due to its unique chemical properties, it can participate in the synthesis and modification of materials. For example, in the preparation of some polymer materials, adding an appropriate amount of N '-hydroxypyridine-2-formamidine can change the physical properties of the material, such as enhancing the stability of the material and improving its mechanical strength. This allows materials to have more choices and optimization directions in fields that require strict material properties such as aerospace and automobile manufacturing.
    Furthermore, in the field of organic synthesis, N' -hydroxypyridine-2-formamidine is often used as an important intermediate. With the active groups in its structure, it can participate in a variety of organic reactions, such as nucleophilic substitution, addition and other reactions. Through these reactions, more complex organic molecular structures can be constructed, which lays the foundation for the synthesis of organic compounds with specific functions, greatly enriching the paths and methods of organic synthesis.
    What are the physical properties of N -HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE?
    The physical properties of N '-hydroxypyridine-2-formamidine are particularly important and are related to many uses and characteristics.
    Looking at its appearance, it is mostly white to off-white crystalline powder. This morphological state is helpful in identifying and preliminarily judging its quality. Its texture is fine, tactile or relatively smooth, and this microscopic characteristic is also one end of its physical manifestation.
    When it comes to solubility, it shows a certain solubility in organic solvents, such as methanol, ethanol, dichloromethane, etc. This property makes it convenient in the field of organic synthesis, in the preparation of reaction systems, and in promoting reaction processes. In water, although the solubility is not as good as that of organic solvents, it also dissolves to a certain extent. This interaction with water molecules affects its behavior in aqueous environments.
    Melting point is a term, the melting point of this substance is about a specific range, and this value is its inherent physical constant. Accurate determination of melting point can not only be used as the basis for purity judgment, but also an indispensable reference in the identification of substances. The determination of melting point also reflects the magnitude and characteristics of the forces between molecules, revealing the law of molecular arrangement and interaction.
    Density is also one of its physical properties. The density value is specific, indicating that the mass of the substance contained in the unit volume is constant. This property is of great significance in the application of materials, in considering the mixing ratio with other substances, filling effect, etc.
    In addition, its stability also belongs to the category of physical properties. Under normal temperature and pressure, N '-hydroxypyridine-2-formamidine is relatively stable, and may change under high temperature, high humidity or specific light conditions. Understanding this stability provides key guidelines for ensuring its quality during storage and transportation.
    What is the synthesis method of N -HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE?
    To prepare N '-hydroxypyridine-2-formamidine, the method is as follows:
    Starting material, pyridine-2-formonitrile is often selected. This is because in the structure of pyridine-2-formonitrile, the cyanyl activity is quite good, which can be used for subsequent reaction conversion.
    The first step is to add an appropriate amount of basic catalyst, such as potassium carbonate, to pyridine-2-formonitrile and hydroxylamine in a suitable solvent, such as ethanol. This alkaline environment can promote the reaction. The nucleophilic addition reaction occurs between the two. The carbon atom of the cyanyl group is attacked by the nucleophilic attack of the nitrogen atom in the hydroxylamine, and then forms an intermediate product.
    This intermediate product needs to be further transformed. Then, the pH of the reaction system is adjusted to be weakly acidic, or a little dilute hydrochloric acid can be added. Under these conditions, the intermediate undergoes intramolecular rearrangement and hydrolysis, and after electron transfer and chemical bond rearrangement, the final product is N '-hydroxypyridine-2-formamidine.
    After the reaction is completed, the product is separated and purified. First, most of the solvents in the reaction system are removed by vacuum distillation. Then, column chromatography is performed. Silica gel is used as the fixed phase, ethyl acetate and petroleum ether in a suitable ratio are used as the mobile phase, and the difference in the distribution coefficient between the fixed phase and the mobile phase between the product and the impurity is used to realize the purification of the product. Thus, pure N '-hydroxypyridine-2-formamidine can be obtained.
    What are the precautions in the use of N -HYDROXYPYRIDINE-2-CARBOXIMIDAMIDE?
    For N '-hydroxypyridine-2-formamidine, many things need to be paid attention to when using it.
    First, the toxicity and safety of this product must be carefully observed. Although its exact toxicity is not known, many chemicals are potentially harmful. When taking it, protective gear, such as gloves, goggles, masks, etc., are indispensable to prevent skin, eyes and respiratory tract from being damaged. If you accidentally touch it, rinse it with plenty of water quickly, and seek medical attention as soon as possible.
    Second, storage methods are also important. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because many chemical substances are easy to react with the surrounding environment, improper storage, or deterioration, or dangerous. And must be stored separately from oxidizing agents, acids, bases, etc., to prevent mutual reaction and cause disasters.
    Third, during use, the operation must be accurate and standardized. According to the established process and dosage, do not be good at increasing or decreasing. Chemical experiments, millimeter difference, or cause very different results, or even cause safety accidents. If solution preparation is involved, pay attention to the selection and proportion of solvents to ensure their solubility and stability.
    Fourth, it is essential to know its chemical properties and reaction mechanism. Understand its reaction trend under different conditions in order to avoid harmful reactions. If you encounter some reagents, or there is gas escape, heat release, etc., you can take precautions if you know in advance.
    Fifth, the ventilation of the experimental site should not be neglected. Good ventilation can disperse harmful gases in time to ensure the health of the experimenter, and also prevent gas accumulation and explosion. In short, the use of N '-hydroxypyridine-2-formamidine requires caution everywhere to ensure safety and effectiveness.