N N Diethylpyridine 3 Carboxamide
pyridine pyrrole pyrazine piperidine piperazine

N,N-diethylpyridine-3-carboxamide

    Specifications

    HS Code

    322892

    Chemical Formula C10H14N2O
    Molar Mass 178.23 g/mol
    Appearance Typically a solid (physical state may vary based on conditions)
    Melting Point Specific value would depend on purity and experimental conditions
    Boiling Point Boiling point information varies by purity and external conditions
    Solubility In Water Limited solubility in water, being an organic compound
    Solubility In Organic Solvents Soluble in many common organic solvents like ethanol, chloroform
    Density Density data depends on physical state and conditions
    Vapor Pressure Low vapor pressure as it is often in solid state under normal conditions
    Odor May have a faint, characteristic organic odor

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    General Information
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    Frequently Asked Questions

    As a leading N,N-diethylpyridine-3-carboxamide 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-diethylpyridine-3-carboxamide?
    The chemical structure of N, N-diethylpyridine-3-formamide is one of the structures of organic compounds. Looking at its name, it can be seen that this compound contains a pyridine ring, which is a six-membered heterocyclic ring with a nitrogen atom in it, which is aromatic. The third position of the pyridine ring is connected with a formamide group, that is, the -CONH-structure, and the nitrogen atom of this amide group is connected with two ethyl groups, that is, -C ² H groups. In this structure, the pyridine ring endows the compound with certain stability and unique electron cloud distribution, and the formamide group is introduced into the polar group, which affects the physical and chemical properties of the compound, such as solubility and reactivity. The existence of two ethyl groups also affects the properties of the compound, such as increasing its fat solubility. Such a structure makes N, N-diethylpyridine-3-formamide have unique uses and reaction characteristics in organic synthesis, medicinal chemistry and other fields.
    What are the main uses of N-diethylpyridine-3-carboxamide?
    N, N-diethylpyridine-3-formamide is one of the organic compounds. It has a wide range of uses in the field of medicine and is often a key intermediate for the creation of new drugs. Because the compound has a specific chemical structure and activity, it can be chemically modified to generate derivatives with pharmacological activity, and then used in the treatment of diseases.
    In the field of materials science, there is also no shortage of its use. Or it can be used as a synthetic raw material for special functional materials. After specific reactions, materials with unique properties can be constructed, such as those with special optical and electrical properties, which are used in optoelectronic devices and other fields.
    In addition, it is an important chemical reagent in scientific research and exploration. Chemists use it to participate in a variety of organic reactions, explore reaction mechanisms, expand organic synthesis paths, and contribute to the development of organic chemistry. Due to the properties of pyridine rings and amide groups in its structure, it can exhibit a variety of chemical behaviors and provide rich research materials for scientific research.
    In summary, N, N-diethylpyridine-3-formamide has indispensable and important uses in many aspects such as medicine, materials, and scientific research.
    What are the physical properties of N-diethylpyridine-3-carboxamide?
    N, N-diethylpyridine-3-formamide is one of the organic compounds. Its physical properties are quite unique, let me tell them one by one.
    This substance is usually in the shape of a solid state at room temperature. Looking at its appearance, it may be a white crystalline powder with uniform and fine quality, like frost and snow, smooth and not dazzling. Its melting point is within a specific range, and this temperature value is crucial for identifying and purifying this substance. It is like a door to precision, leading to the mystery of its characteristics.
    When it comes to solubility, it shows a different affinity in organic solvents. For example, in organic solvents such as ethanol and ether, it can dissolve well, just like a fish entering water, and it fuses seamlessly. This solubility is due to the special interaction between its molecular structure and the molecules of the organic solvent, or van der Waals force, or hydrogen bond, etc., so that the two are closely combined. However, in water, its solubility is relatively limited, like oil and water, it is difficult to completely blend, and this characteristic is also due to its hydrophobic groups.
    Its density is also fixed. This value reflects the mass per unit volume of the substance, which is its inherent property, just like a human fingerprint, and is unique. The density is related to many practical applications, such as in separation, mixing, etc., all need to consider this factor.
    Furthermore, the boiling point of this substance is also an important physical parameter. The boiling point is the critical temperature at which a substance changes from a liquid to a gaseous state. Above this temperature, the form of the substance will undergo qualitative changes. Knowing the boiling point is of great significance in the operation of distillation and purification processes, just like a beacon on a ship, guiding the operation direction.
    In addition, its refractive index cannot be ignored. The refractive index reflects the degree to which the direction of light propagation in the substance changes, just like the "bending code" of light, which can be used to identify the purity and concentration of the substance. It has a significant role in the field of analysis and detection.
    This is the approximate physical properties of N, N-diethylpyridine-3-formamide, which are related to each other and together outline its unique physical "picture".
    What are the synthesis methods of N, N-diethylpyridine-3-carboxamide
    To prepare N, N-diethylpyridine-3-formamide, there are two common methods. First, pyridine-3-formic acid is used as the starting material. First, pyridine-3-formic acid is heated with thionyl chloride, which is the step of acid chlorination. Pyridine-3-formic acid can be converted into pyridine-3-formyl chloride, and the reaction is violent. It needs to be controlled at temperature and done in a well-ventilated place. After obtaining pyridine-3-formyl chloride, it is slowly dripped into the organic solution of diethylamine. This step is an amidation reaction, which should be stirred at low temperature and fully to prevent side reactions. After dripping, continue to stir, until the reaction is complete, purify by conventional methods, such as column chromatography, recrystallization, etc., pure N, N-diethylpyridine-3-formamide can be obtained.
    Second, pyridine-3-formate ethyl ester is used as the starting material. First, ethyl pyridine-3-formate is mixed with diethylamine, an appropriate amount of catalyst, such as potassium carbonate, is added, and the reaction is refluxed at an appropriate temperature. This reaction is based on the principle of ester exchange. The ethoxy group of ethyl pyridine-3-formate is replaced by the amino group of diethylamine to form N, N-diethylpyridine-3-formamide. After the reaction is completed, the target product can also be obtained through washing with water, liquid separation, drying, and vacuum distillation. These two methods have their own advantages and disadvantages. The former reaction step is slightly more complicated, but the yield may be higher; the latter step is slightly simpler, but the control requirements for the reaction conditions may be stricter. In practice, the choice should be based on a comprehensive balance of factors such as raw material availability, cost, and product purity.
    N, N-diethylpyridine-3-carboxamide what are the precautions during use
    For N, N-diethylpyridine-3-formamide, many matters need to be paid attention to when using it. This substance has specific chemical properties and is safe when used. Because it may be potentially dangerous, protection must be taken when exposed. Handle this object in front of suitable protective equipment, such as gloves, goggles and protective clothing, to prevent skin and eyes from coming into contact with it and causing injury.
    In addition, its stability under specific conditions also needs to be concerned. Avoid high temperatures, open flames and strong oxidants, which may cause the risk of ignition. When storing, it should be placed in a cool, dry and well-ventilated place, and properly stored according to regulations to prevent leakage. If there is a leakage, take immediate and proper measures to dispose of it, so as not to cause environmental pollution due to diffusion.
    During use, accurate control of the dosage is also the key. According to the needs of experiment or production, accurately measure and use, do not overuse, avoid material waste, and avoid the difficulty of subsequent treatment. At the same time, be familiar with its reaction characteristics. When participating in chemical reactions, clarify its role with other substances, follow the correct operation process, and ensure a smooth and safe reaction.
    In addition, after use, the disposal of residual substances should not be ignored. Proper disposal according to regulations, do not dispose of at will, to protect the environment and the safety of others. In short, with N, N-diethylpyridine-3-formamide, safety, standardization, and accuracy are essential, and all links should be treated with caution in order to achieve the expected purpose and avoid accidents.