3 5 Dichloro 2 Hydroxymethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3,5-dichloro-2-(hydroxymethyl)pyridine

    Specifications

    HS Code

    118213

    Name 3,5 - dichloro - 2 - (hydroxymethyl)pyridine
    Molecular Formula C6H5Cl2NO
    Molecular Weight 178.016 g/mol
    Appearance Typically a solid (appearance may vary depending on purity and conditions)
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility In Water Limited solubility likely, as pyridine ring and chloro - groups reduce water - solubility, but hydroxyl - methyl group may enhance it slightly
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane due to its organic nature
    Pka The pyridine nitrogen can be protonated, pKa value relevant for acid - base behavior (experimental determination required)
    Density Data may vary, needs experimental determination
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    Frequently Asked Questions

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    What are the main uses of 3,5-dichloro-2- (hydroxymethyl) pyridine?
    3,5-Dioxide-2- (methoxy) pyridine has the following main uses:
    In the field of pharmaceutical chemistry, 3,5-dioxide-2- (methoxy) pyridine is often used as a key intermediate. The synthesis of many drugs is based on this as the starting material, and through a series of chemical transformations, complex molecular structures with specific pharmacological activities are constructed. For example, in the creation of some antibacterial drugs, it participates in key cyclization and functional group modification steps, which plays a decisive role in the precise regulation of the antibacterial activity of drug molecules, helping to develop better antibacterial agents with fewer side effects.
    In the field of materials science, it also shows unique value. Due to its special chemical structure endowing certain electronic properties and stability, it is widely used in the synthesis of functional materials. For example, the preparation of organic semiconductor materials with specific photoelectric properties, 3,5-dioxide-2- (methoxy) pyridine can participate in the molecular design of materials, optimize the electron transport capacity and optical absorption properties of materials, and then promote the development of organic electronic devices, such as organic Light Emitting Diodes (OLEDs) and organic solar cells.
    In organic synthetic chemistry, as an important building block, it provides a variety of possibilities for the construction of organic molecules. With its multiple activity check points, it can react with other organic reagents through different reaction paths to construct complex carbon-heteroatom bonds, realize the efficient construction of complex organic molecular skeletons, greatly enrich the strategies and methods of organic synthesis, and lay the foundation for the creation of new organic compounds.
    What are the physical properties of 3,5-dichloro-2- (hydroxymethyl) pyridine
    The physical properties of 3,5-dioxy-2- (hydroxymethyl) furan are as follows:
    This substance is mostly solid at room temperature and has a certain crystallinity. It may be white to off-white crystalline powder, which is fine and uniform. Its melting point is about a specific range. Due to the exact value being affected by factors such as impurity content and determination method, it usually fluctuates within a certain range. It is the critical temperature for the substance to transform from solid to liquid, which is of great significance in chemical synthesis, purity identification and other fields.
    This substance has different solubility in common organic solvents. In polar organic solvents, such as methanol and ethanol, by virtue of the formation of hydrogen bonds or dipole-dipole interactions between molecules and solvent molecules, it exhibits good solubility and can be mutually soluble in a certain proportion to form a clear and transparent solution, which is crucial for its chemical reaction, separation, purification and analysis in the solution; while in non-polar organic solvents, such as n-hexane and toluene, due to the difference in molecular polarity, the solubility is poor, only slightly soluble or almost insoluble.
    Its density is also an important physical property. Although the exact value needs to be determined by precise experiments, it can be predicted to be similar to the density of common organic compounds according to its molecular structure and relative molecular mass. It has important reference value for its phase behavior and mixed system stability in practical applications. In addition, the substance may have a specific odor, but the odor is usually weak and requires careful sniffing under certain conditions to detect it.
    What are the chemical synthesis methods of 3,5-dichloro-2- (hydroxymethyl) pyridine?
    To prepare 3-2,5-dichloro-2- (methoxy) pyridine, there are various methods for its synthesis.
    First, it can be started from a suitable pyridine derivative. First, a specific position on the pyridine ring is halogenated to introduce chlorine atoms. If a pyridine compound is used as a substrate, under appropriate reaction conditions, such as in the presence of a specific solvent or catalyst, the chlorine atom can be introduced into the 2,5-position. Subsequently, another position is methoxylated. Reagents containing methoxy groups can be used to react with halogenated pyridine derivatives in an alkaline environment or a specific catalytic system to replace the corresponding hydrogen atoms with methoxy groups to obtain the target product.
    Second, it can also be synthesized by the strategy of constructing a pyridine ring. First, use suitable raw materials to construct a pyridine ring through a series of reactions such as condensation and cyclization. For example, select a small molecule compound containing appropriate functional groups, and under certain temperature, pressure and catalyst action, make it undergo a condensation reaction to form a pyridine ring structure. During or after cyclization, various reaction conditions are cleverly used to gradually introduce chlorine atoms and methoxy groups. For example, chlorine atoms are introduced first, and then methoxy groups are introduced through nucleophilic substitution in subsequent steps, and the reaction sequence and conditions are carefully adjusted to achieve the synthesis target.
    Third, the existing simple compounds containing chlorine and methoxy groups can also be considered as raw materials to construct the target molecule through coupling reaction. Select suitable coupling reagents and catalysts to couple the chlorine-containing pyridine derivative fragment with the methoxy-containing fragment in a specific reaction system, so as to splice to form 3-2,5-dichloro-2- (methoxy) pyridine. This process requires precise control of reaction conditions to ensure the selectivity and yield of the coupling reaction.
    What are the precautions for storing and transporting 3,5-dichloro-2- (hydroxymethyl) pyridine?
    During the storage and transportation of 3% 2C5-dioxy-2- (hydroxymethyl) furan, the following key points should be paid attention to:
    First, when storing, be sure to choose a cool, dry and well-ventilated place. This substance is extremely sensitive to temperature and humidity, and high temperature and humidity can easily cause it to deteriorate. If the storage environment temperature is too high, or chemical reactions are triggered, resulting in changes in the properties of the substance; if the humidity is too high, it may cause it to absorb moisture, which in turn affects the purity and stability. Therefore, every effort should be made to maintain the temperature and humidity of the storage environment within the appropriate range.
    Second, it is necessary to strictly avoid contact with oxidants, acids, bases and other substances. 3% 2C5-dioxy-2- (hydroxymethyl) furan is chemically active, and contact with the above substances is likely to trigger violent chemical reactions, such as combustion, explosion and other serious consequences. Therefore, when storing, it is necessary to store it separately from these dangerous substances, and set up prominent signs as a warning.
    Third, the choice of storage containers is also crucial. Containers with good corrosion resistance and sealing should be selected to prevent material leakage. At the same time, the material of the container must not chemically react with the substance to ensure the safety of the storage process. On the outside of the container, key information such as the name of the substance, specifications, and production date should be clearly marked to facilitate management and traceability.
    Fourth, during transportation, it is necessary to ensure that the transportation vehicle is in good condition and has corresponding safety protection measures. Transportation vehicles should be equipped with fire extinguisher materials, leakage emergency treatment equipment, etc., to deal with emergencies. In addition, bumps and vibrations should be avoided during transportation to prevent damage to the container and cause material leakage.
    Fifth, transportation personnel must undergo professional training, familiar with the dangerous characteristics of the substance and emergency treatment methods. In the event of leakage and other unexpected situations during transportation, transportation personnel can quickly and accurately take emergency measures to reduce hazards. For example, if a small amount of leakage occurs, it can be mixed with sand, dry lime, or soda ash and collected in a dry, clean, covered container; if a large amount of leakage occurs, a dike or pit should be built to contain it, covered with foam, to reduce steam disasters, and promptly report to relevant departments for professional rescue.
    What are the effects of 3,5-dichloro-2- (hydroxymethyl) pyridine on the environment and human health?
    The effects of 3% 2C5-dioxy-2- (methoxy) benzene on the environment and human health are as follows:
    In terms of the environment, if this substance enters the natural water body, it may interfere with the aquatic ecosystem. Due to its special chemical structure, some aquatic organisms are difficult to decompose and metabolize it, and may accumulate in organisms. For a long time, this may change the behavior pattern, growth rate and even reproduction ability of aquatic organisms, and destroy the ecological balance of water bodies. If it is released into the atmosphere, under conditions such as light, or participates in complex photochemical reactions, it generates secondary pollutants, affects air quality, and may spread with the atmospheric circulation, affecting the regional and even global atmospheric environment. In soil, it may change the physical and chemical properties of the soil, affect the structure and function of soil microbial community, and then have an indirect impact on plant growth and development, hinder plant absorption of nutrients, interfere with plant hormone balance, etc.
    As far as human health is concerned, inhalation of this substance through the respiratory tract may irritate the mucosa of the respiratory tract, causing symptoms such as cough, asthma, breathing difficulties, etc. Long-term exposure may also damage lung tissue and increase the risk of respiratory diseases, such as chronic obstructive pulmonary disease, lung cancer, etc. If it is exposed to the skin, it may have certain irritation and allergenicity, causing allergic reactions such as skin redness, itching, rashes, and even entering the blood circulation through the skin barrier, causing damage to important organs such as the liver and kidneys, and affecting the normal metabolism and detoxification function of the organs. If accidentally ingested, it can damage the digestive system, nausea, vomiting, abdominal pain, diarrhea and other symptoms, and life-threatening in severe cases. In short, 3% 2C5-dioxy-2- (methoxy) benzene has potential harm to the environment and human health, and needs to be strictly prevented and managed in production and use.