5 Methyl 2 Pyridinemethanol
pyridine pyrrole pyrazine piperidine piperazine

5-Methyl-2-pyridinemethanol

    Specifications

    HS Code

    139349

    Chemical Formula C7H9NO
    Molar Mass 123.15 g/mol
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Melting Point Typically around 50 - 55 °C
    Solubility In Water Moderate solubility, can form hydrogen bonds with water
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Density Approximate density value could be in the range typical for similar organic compounds, around 1.1 g/cm³ (estimated)

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    General Information
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    Frequently Asked Questions

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    What are the physical properties of 5-Methyl-2-pyridinemethanol?
    5 - Methyl - 2 - pyridinemethanol is an organic compound with unique physical properties, which is described in detail by you today.
    Looking at its properties, under normal temperature and pressure, 5 - Methyl - 2 - pyridinemethanol is often in the state of white to light yellow crystalline powder, which makes it easy to identify in appearance, just like finely crushed crystalline powder, fine and uniform.
    When it comes to the melting point, the melting point of this compound is within a certain range. At about a certain temperature, it gradually melts from a solid state to a liquid state. The characteristics of this melting point are an important basis for identifying this substance. In many experiments and industrial applications, its purity and authenticity can be preliminarily judged.
    Boiling point is also one of its key physical properties. When a specific high temperature is reached, 5-Methyl-2-pyridinemethanol will convert from liquid to gaseous state. This boiling point data is of great significance in separation, purification and other processes, and is related to the setting and control of operating conditions.
    In terms of solubility, it exhibits a certain solubility in specific organic solvents. For example, in some common organic solvents, it can be partially or completely dissolved. This property is of great significance in organic synthesis and other fields. It can help chemists choose suitable solvents to achieve smooth reaction or effective separation of products. The value of
    density is also its physical characterization. This value reflects the mass of its unit volume. In many scenarios involving quantitative treatment of substances and process design, density data provides necessary support for accurate calculation and operation.
    The physical properties of 5-Methyl-2-pyridinemethanol, from appearance, melting point, boiling point, solubility to density, are its "business card" in the field of chemistry. Chemists can use this material in scientific research and industrial practice through in-depth understanding and precise grasp of these properties, and promote the progress of the chemical industry.
    What are the chemical properties of 5-Methyl-2-pyridinemethanol?
    5-Methyl-2-pyridyl methanol is one of the organic compounds. It has the following chemical properties:
    This substance contains a pyridine ring and a methanol group. The pyridine ring is aromatic and has certain stability and unique electronic properties. Due to the presence of nitrogen atoms, the pyridine ring can participate in various reactions, such as nucleophilic substitution reactions. Nitrogen atoms have solitary pairs of electrons and can be used as electron donors to react with electrophilic reagents. The presence of the methanol group gives the compound a certain hydrophilicity. Hydroxy (-OH) groups can participate in many reactions, such as esterification reactions, and carboxylic acids can form ester compounds under acid catalysis; oxidation reactions can also occur. If treated with appropriate oxidants, they can be oxidized to aldehyde groups or carboxylic groups.
    From the perspective of spatial structure, the pyridine ring has a planar structure, and the whole molecule of 5-methyl-2-pyridine methanol has a specific spatial orientation, which has a great influence on its physical and chemical properties. The steric resistance of different substituents will affect the reactivity and selectivity.
    In addition, 5-methyl-2-pyridylmethanol can be used as a ligand to form complexes with metal ions due to its heteroatoms such as nitrogen and oxygen, and may have potential applications in catalysis, materials science and other fields. The chemical properties of this compound have attracted much attention in organic synthesis, medicinal chemistry and other fields, and can be used as a key intermediate for the synthesis of more complex organic compounds.
    What are the main uses of 5-Methyl-2-pyridinemethanol?
    5-Methyl-2-pyridinemethanol, Chinese name 5-methyl-2-pyridinemethanol, has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate for the synthesis of a variety of drugs. Due to its structural properties of pyridine and methanol, it can participate in a variety of chemical reactions and be modified to construct complex active molecular structures. For example, when developing new drugs for the treatment of specific diseases, it can be used to introduce specific groups to change the activity, solubility and stability of drug molecules.
    In the field of organic synthesis, 5-methyl-2-pyridinemanol is a commonly used starting material and reaction reagent. The existence of the pyridine ring endows it with unique electronic properties, making the related reactions highly selective and reactive. For example, when building a nitrogen-containing heterocyclic compound system, it can react with other compounds through condensation and substitution to form novel compounds, providing organic synthetic chemists with more possibilities for molecular design and construction.
    In addition, it has also emerged in the field of materials science. In the preparation of some functional materials, 5-methyl-2-pyridyl methanol can be used as a modifier or structure-directing agent. With its special structure, the microstructure and properties of the material can be regulated, such as affecting the pore structure and surface properties of the material, so as to optimize the performance of the material in adsorption, catalysis and electron transport. In short, 5-methyl-2-pyridyl methanol plays an important role in many fields due to its unique structure, promoting the development of technologies and products in various fields.
    What are 5-Methyl-2-pyridinemethanol synthesis methods?
    The synthesis method of 5-methyl-2-pyridinomethanol has been known in ancient times, and is described in this article.
    First, 5-methyl-2-pyridinecarboxylic acid is used as the starting material. This is a common method. First, 5-methyl-2-pyridinecarboxylic acid is reacted with a strong reducing agent, such as lithium aluminum hydride, in a suitable organic solvent, such as anhydrous tetrahydrofuran, under low temperature and strict anhydrous and anaerobic conditions. Lithium aluminum hydride is highly reducing, and carboxyl groups can be reduced to hydroxymethyl groups to obtain 5-methyl-2-pyridinecarboxylic alcohol. After the reaction is completed, the reaction system needs to be carefully handled. The excess aluminum hydride lithium is carefully hydrolyzed with dilute acid, and then the product is purified through extraction, washing, drying, distillation and other steps.
    Second, starting from 5-methyl-2-halopyridine. Halopyridine has high activity and can react with metal magnesium to make Grignard reagent. 5-methyl-2-halopyridine and magnesium chips are placed in anhydrous ether to initiate a reaction to obtain Grignard reagent. Then, the ether solution of formaldehyde is slowly added to the Grignard reagent. The Grignard reagent undergoes a nucleophilic addition reaction with formaldehyde. After hydrolysis, 5-methyl-2-pyridine methanol can also be obtained. Subsequent operations also need to go through a series of separation and purification operations to obtain a purified product.
    Third, 5-methylpyridine is used as a raw material. 5-methylpyridine can be halogenated by side chain first. For example, N-bromosuccinimide (NBS) is used in the presence of an initiator to replace the hydrogen on the methyl group of the side chain of the pyridine with a bromine atom to generate 5-methyl-2-bromomethylpyridine. This bromomethylpyridine is then reacted with nucleophiles, such as methanol solution of sodium methoxide, the bromine atom is replaced by methoxy group, and then hydrolyzed to convert into 5-methyl-2-pyridine methanol. Finally, the product is further purified by recrystallization, column chromatography and other methods.
    These are all methods for synthesizing 5-methyl-2-pyridine methanol, each has its own advantages and disadvantages, and needs to be selected according to the actual situation.
    5-Methyl-2-pyridinemethanol What are the precautions in storage and transportation?
    5-Methyl-2-pyridyl methanol is an organic compound. During storage and transportation, the following things should be paid attention to:
    First, when storing, it should be placed in a cool, dry and well-ventilated place. This is because it has certain chemical activity, high temperature, humid environment or cause it to deteriorate. If it is in a high temperature, it may cause a chemical reaction and change its chemical structure; in a humid environment, or absorb moisture, which affects the purity.
    Second, it must be stored separately from oxidizing agents, acids and other substances. The chemical properties of 5-methyl-2-pyridyl methanol determine that it comes into contact with oxidants or reacts violently, and even causes dangers such as combustion and explosion; coexists with acid substances, or reacts with acid and base, causing it to fail or form dangerous products.
    Third, choose the appropriate material for the storage container. In general, corrosion-resistant containers, such as glass or specific plastic materials, should be used. Because of its reaction with certain metal materials, the container will corrode and also affect the purity of the substance.
    Fourth, during transportation, it is necessary to ensure that the container is well sealed. To prevent leakage, if it leaks into the environment, or causes pollution to the environment, and the substance may be harmful to the human body, once leaked, or endanger the health of the transporter and surrounding people.
    Fifth, relevant regulations and standards must be followed when transporting such chemical substances. Professional qualifications and licenses are required for transporting such chemical substances, and professional training is also required for transporters to be familiar with their hazards and emergency treatment methods, so as to ensure transportation safety and avoid accidents.