6 Chloropyridine 3 Carboxaldehyde
pyridine pyrrole pyrazine piperidine piperazine

6-Chloropyridine-3-carboxaldehyde

    Specifications

    HS Code

    487164

    Name 6-Chloropyridine-3-carboxaldehyde
    Molecular Formula C6H4ClNO
    Molecular Weight 141.55
    Appearance Pale yellow to light brown solid
    Cas Number 13066-04-1
    Boiling Point 243 - 245 °C
    Melting Point 52 - 56 °C
    Density 1.328 g/cm³
    Solubility Soluble in organic solvents like ethanol, acetone
    Flash Point 100.7 °C
    Purity Typically high - purity grades available, e.g., 98%+

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    General Information
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    Frequently Asked Questions

    As a leading 6-Chloropyridine-3-carboxaldehyde 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 6-Chloropyridine-3-carboxaldehyde?
    6-Chloropyridine-3-formaldehyde is one of the organic compounds. Its physical properties are particularly important and are related to many chemical applications.
    This compound is generally in a solid state at room temperature, and it may be white to light yellow powder or crystalline. This is a common physical appearance. Its melting point and boiling point also have specific values. The melting point is about [specific melting point value], and the boiling point is about [specific boiling point value]. The determination of the melting point is related to its purity and the initial temperature of the thermal change, and the boiling point is the key temperature point at which the substance changes from liquid to gaseous state. Both of these are important basis for the identification and separation of the compound.
    Furthermore, its solubility cannot be underestimated. In common organic solvents, such as ethanol, ether, etc., 6-chloropyridine-3-formaldehyde may have certain solubility. In ethanol, it may be moderately soluble, but in water, its solubility is quite limited. The difference in solubility is due to the characteristics of its molecular structure, the polarity of the molecule, and the interaction force with the solvent molecule, resulting in different solubility in different solvents.
    The density is also one of its physical properties. Its density is about [specific density value], which reflects the mass per unit volume of the substance, and is of great significance in chemical production and experimental operations, for accurate measurement, mixing ratio determination, etc.
    In addition, the volatility of 6-chloropyridine-3-formaldehyde is relatively low, and it is not easy to evaporate and dissipate at room temperature and pressure. This characteristic also affects its storage and use. When storing, there is no need to worry too much about its rapid volatilization and loss.
    The above physical properties are interrelated and jointly characterize the characteristics of 6-chloropyridine-3-formaldehyde, which lays the foundation for its application in chemical synthesis, drug development and other fields. Chemists can rationally design experiments and select processes according to these properties to achieve the desired chemical purpose.
    What are the chemical properties of 6-Chloropyridine-3-carboxaldehyde?
    6-Chloropyridine-3-formaldehyde is one of the organic compounds. It has unique chemical properties and is widely used in the field of organic synthesis.
    This compound contains chlorine atoms and aldehyde groups. Chlorine atoms have electron-absorbing properties, which can affect the distribution of molecular electron clouds, reduce the density of adjacent and para-potential electron clouds, and cause different electrophilic substitution reactivity. Electrophilic reagents are easy to attack the relatively high electron cloud density of the pyridine ring. Chlorine atoms also make the compound have a certain polarity, which affects its solubility and reactivity.
    aldehyde groups are the key functional groups of this compound and have high reactivity. Many typical aldehyde reactions can occur, such as oxidation reactions. Under the action of suitable oxidizing agents, aldehyde groups can be oxidized to carboxyl groups to form 6-chloropyridine-3-carboxylic acids; in reduction reactions, aldehyde groups can be reduced to alcohol hydroxyl groups to obtain 6-chloropyridine-3-methanol. And aldehyde groups can condensate with compounds containing active hydrogen, such as amines and alcohols. Reaction with amines can form imines, and reaction with alcohols produces acetals. Such reactions are often used in organic synthesis as means of functional group conversion and protection.
    6-chloropyridine-3-formaldehyde is active due to the synergistic effect of pyridine ring, chlorine atom and aldehyde group. It is an important intermediate in drug synthesis, materials science and other fields. It can construct complex organic molecular structures through various reactions.
    What are the common synthetic methods of 6-Chloropyridine-3-carboxaldehyde?
    The common synthesis methods of 6-chloropyridine-3-formaldehyde are the key content of chemical synthesis. There are various methods, and each has its own advantages, which must be selected according to the specific situation and needs.
    One is the method of using 6-chloronicotinic acid as the starting material. First, 6-chloronicotinic acid and suitable reducing agents, such as lithium aluminum hydride (LiAlH), are used under suitable reaction conditions. In this reaction, lithium aluminum hydride has strong reductive properties, and the carboxyl group (-COOH) of 6-chloronicotinic acid can be reduced to hydroxymethyl (-CH 2O OH) to obtain 6-chloropyridine-3-methanol. Then, 6-chloropyridine-3-methanol is oxidized in a specific solvent with a mild oxidizing agent, such as manganese dioxide (MnO ²), to convert the hydroxymethyl group into an aldehyde group (-CHO), and finally 6-chloropyridine-3-formaldehyde.
    The second is the route using 3-cyano-6-chloropyridine as a raw material. After the hydrolysis of 3-cyano-6-chloropyridine, the cyano group (-CN) can be converted into a carboxyl group to obtain 6-chloronicotinic acid. This step needs to be carried out under acidic or alkaline conditions. Then with the above method of using 6-chloronicotinic acid as raw material, the target product is obtained by reduction and oxidation.
    There is also a method of synthesizing pyridine derivatives by halogenation, formylation and other series of reactions. First, the pyridine derivatives are halogenated, and chlorine atoms are introduced at suitable positions to obtain 6-chloropyridine derivatives. After that, suitable formylation reagents, such as the combination of DMF (N, N-dimethylformamide) and phosphorus oxychloride (POCl), are selected to formylate 6-chloropyridine derivatives, and aldehyde groups are introduced at 3 positions to obtain 6-chloropyridine-3-formaldehyde.
    All synthesis methods have advantages and disadvantages. The method using 6-chloronicotinic acid as raw material has relatively clear steps, but some reagents such as lithium aluminum hydride are highly active and dangerous, so the operation needs to be cautious. Using 3-cyano-6-chloropyridine as raw material, the hydrolysis step may involve more complex reaction conditions to control. Pyridine derivatives are halogenated and formylated. Although the choice of raw materials is diverse, multiple steps may reduce the total yield, and each step needs to be precisely controlled to ensure the purity of the product. In actual synthesis, when considering factors such as raw material availability, cost, controllability of reaction conditions, product purity and yield, the optimal synthesis path is selected.
    6-Chloropyridine-3-carboxaldehyde in what areas
    6-Chloropyridine-3-formaldehyde is useful in many fields such as medicine, pesticides and materials.
    In the field of medicine, it can be regarded as a key traditional Chinese medicine, often used as an intermediate for the synthesis of various drugs. For example, when synthesizing some drugs with antibacterial and anti-inflammatory effects, 6-chloropyridine-3-formaldehyde plays an important role in building the molecular framework of drugs. With its unique chemical structure, ingenious reactions with other compounds, and a series of fine chemical transformations, complex drug molecules with specific pharmacological activities are gradually constructed.
    In the field of pesticides, this compound is also indispensable. Using it as a starting material, a class of highly efficient insecticides or fungicides can be synthesized. Its chemical properties enable it to combine with specific biological targets, interfere with the nervous system of pests, or hinder the metabolic process of pathogens, so as to achieve good pest control effects, help agriculture harvest, and keep crops thriving.
    In the field of materials, 6-chloropyridine-3-formaldehyde can participate in the creation of functional materials. For example, in the synthesis of organic optoelectronic materials, it can be used as a key structural unit to endow materials with special photoelectric properties. Through ingenious molecular design and synthesis strategies, it is introduced into the molecular structure of materials, so that the materials exhibit excellent properties in light absorption, charge transport, etc., paving the way for the development and application of new optoelectronic materials.
    In conclusion, although 6-chloropyridine-3-formaldehyde is an organic compound, it plays a significant role in many fields, just like a shining chemical pearl, shining brightly on the stage of human production and life.
    What is the market price of 6-Chloropyridine-3-carboxaldehyde?
    6-Chloropyridine-3-formaldehyde, this substance is in the market, and its price often changes due to many reasons. The various merchants in the city have different prices because of their quality and quantity.
    In the path of ordinary trade, if the purchase quantity is quite small, it is only for small trials or research needs, and its price may be high. Cover the preparation of the process and complexity, the purification technique is difficult, and the small amount of transactions, the operator in order to protect their profits, so the price is high. The price per gram, or up to tens of gold spectrum.
    If it is a batch purchase, the industry considers the efficiency of scale and the cost of apportionment, and the price should be reduced. If you buy hundreds of grams or even thousands of grams, the price per gram may be reduced to more than ten gold.
    And the supply and demand of the market also affect the price. If there are many people who want it, but there are few suppliers, the price will inevitably rise; if the supply exceeds the demand, the business will sell it quickly, or reduce the price to promote the transaction.
    The distance of the place of origin, the cost of transportation, and the difference in time are all related to the price. Produced in distant places, with the addition of freight, the price will be high; when raw materials are scarce and government orders change, the price may also change significantly.
    To know the exact price, you should consult the merchants who specialize in the cities, and compare the reports of the various families to understand its current value.