6 Methylpyridine 3 Carbonitrile
pyridine pyrrole pyrazine piperidine piperazine

6-Methylpyridine-3-carbonitrile

    Specifications

    HS Code

    845646

    Name 6-Methylpyridine-3-carbonitrile
    Molecular Formula C7H6N2
    Molecular Weight 118.14 g/mol
    Appearance Solid (predicted)
    Boiling Point 236.8°C at 760 mmHg (predicted)
    Melting Point 45 - 49 °C
    Density 1.06 g/cm³ (predicted)
    Flash Point 97.3°C (predicted)
    Water Solubility Insoluble (predicted)
    Logp 1.23 (predicted)

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    Frequently Asked Questions

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    What is the chemistry of 6-Methylpyridine-3-carbonitrile?
    6 - Methylpyridine - 3 - carbonitrile is an organic compound with unique chemical properties. This compound contains a pyridine ring and methyl and cyanyl groups. Due to its special structure, it has a variety of chemical activities.
    From the perspective of physical properties, it is usually a solid or a liquid, with a specific melting point and boiling point, which is affected by intermolecular forces. Its solubility is also an important property. It has good solubility in organic solvents, and its solubility in water may be limited due to polar differences.
    When it comes to chemical activity, cyanyl is its key activity check point. Cyanyl groups are electrophilic and can participate in a variety of reactions, such as hydrolysis reactions. Under acidic or alkaline conditions, cyanyl groups can be converted into carboxylic groups to generate 6-Methylpyridine-3-carboxylic acid. In addition, cyanyl groups can also participate in nucleophilic addition reactions, combine with nucleophiles, and expand the molecular structure.
    Methyl groups are attached to pyridine rings, which has an impact on the distribution of electron clouds of compounds. Pyridine rings are aromatic, and the electron density on the ring can be changed by the electron-giving effect of methyl groups, which affects the selectivity of the substitution reaction region on the ring. For example, during electrophilic substitution reactions, the density of methyl ortho-and para-position electron clouds is relatively high, making them more susceptible to
    At the same time, 6-Methylpyridine-3-carbonitrile can be used as a ligand to coordinate with metal ions to form complexes due to nitrogen atoms. This property may have application potential in the fields of catalysis and materials science. In short, the compound exhibits rich chemical properties due to the interaction of various parts in the structure, and has research and application value in many fields such as organic synthesis and medicinal chemistry.
    What are the common synthetic methods of 6-Methylpyridine-3-carbonitrile?
    6-Methylpyridine-3-formonitrile is also an important compound in organic synthesis. There are a few common synthesis methods.
    First, 6-methylpyridine-3-formic acid is used as the starting material, which is reacted with ammonia to form an amide. After treatment with dehydrating agents such as phosphorus pentoxide and phosphorus oxychloride, the amide is dehydrated to obtain 6-methylpyridine-3-formonitrile. In this process, 6-methylpyridine-3-carboxylic acid reacts with ammonia at a suitable temperature and pressure to form an intermediate of amide, followed by the action of a dehydrating agent to remove water molecules and construct nitrile groups.
    Second, the halogenated pyridine derivatives are started. If a suitable halogenated 6-methylpyridine-3-halide is used, and a cyanide reagent such as potassium cyanide, sodium cyanide or cuprous cyanide is used, it is reacted in a suitable organic solvent in the presence of a phase transfer catalyst. The phase transfer catalyst can help the cyanyl group to successfully replace the halogen atom to achieve the synthesis of 6-methylpyridine-3-formonitrile. This reaction requires attention to the activity of the halide, the amount of cyanide reagent and the control of the reaction conditions.
    Third, the construction strategy of the pyridine ring is used. With suitable nitrogen and carbon-containing raw materials, a pyridine ring is constructed by multi-step reaction, and methyl and nitrile groups are introduced at the same time. For example, with suitable unsaturated amines and unsaturated carbonyl compounds, a pyridine ring is formed by cyclization, and then methyl and nitrile groups are introduced at specific positions. This path is more complicated, but the reaction steps can be cleverly designed according to the availability of raw materials and the controllability of the reaction to achieve the synthesis of the target product.
    All kinds of synthesis methods have their own advantages and disadvantages, and they need to be carefully selected according to the actual raw materials, equipment and process requirements in order to achieve efficient and economical synthesis.
    What are the main uses of 6-Methylpyridine-3-carbonitrile?
    6-Methylpyridine-3-carbonitrile, Chinese name 6-methylpyridine-3-formonitrile, is a kind of organic compound. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry. This compound can be converted into a biologically active structure through a specific chemical reaction, and then used to create various drugs.
    It also has its uses in the field of materials science. Or it can participate in the synthesis of polymer materials with unique properties, such as materials with specific electrical and optical properties. In the field of organic synthetic chemistry, 6-methylpyridine-3-formonitrile can participate in a variety of organic reactions, such as nucleophilic substitution, addition reactions, etc., to help build complex organic molecular structures, provide the possibility for the synthesis of new organic compounds, and promote the development of organic synthetic chemistry. In short, 6-methylpyridine-3-formonitrile is of great value in many chemistry-related fields and plays an indispensable role in the research and development of various fields.
    What are the precautions in storage and transportation of 6-Methylpyridine-3-carbonitrile?
    6-Methylpyridine-3-formonitrile is also an organic compound. When storing and transporting, all precautions must not be ignored.
    When storing, the first environment. It should be placed in a cool and ventilated warehouse, away from fires and heat sources. This is because it has certain chemical activity, high temperature or open flame is easy to cause danger. The temperature of the warehouse should be controlled within a reasonable range to prevent material properties from changing.
    Furthermore, it should be stored separately from oxidizing agents, acids, bases, etc., and should not be mixed. The chemical properties of 6-methylpyridine-3-formonitrile make it encounter the above substances, or cause violent chemical reactions, causing disasters such as combustion and explosion.
    Packaging should also be paid attention to. Make sure the packaging is complete and sealed to prevent leakage. If there is a leak, it will not only damage the substance, but also pollute the environment, and even endanger the safety of the surrounding area.
    When transporting, follow the regulations. The transporting vehicle must be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment. During driving, the driver should drive slowly, avoid sudden brakes and sharp turns, and avoid packaging damage.
    When loading and unloading, it is strictly forbidden to drop, touch, and hit to ensure the integrity of the substance and avoid accidents due to improper operation. In this way, the storage and transportation of 6-methylpyridine-3-formonitrile can ensure safety and avoid disasters.
    6-Methylpyridine-3-carbonitrile impact on the environment and human health
    6-Methylpyridine-3-formonitrile, the impact of this substance on the environment and human health is of great concern to the world.
    At the environmental level, if it accidentally flows into the soil, it may cause gradual changes in soil properties. Microorganisms in the soil depend on the suitable environment for existence, and the entry of 6-methylpyridine-3-formonitrile may disturb the metabolism and reproduction of microorganisms, thereby disrupting the soil ecological balance. And it may have a certain residue in the soil, long-term accumulation will gradually damage soil fertility and be unfavorable to plant growth.
    If it flows into the water body, it is quite harmful to aquatic organisms. The gills, liver and other organs of aquatic animals such as fish may be damaged by it, resulting in abnormal physiological functions such as respiration and metabolism. Plankton such as algae are also affected, causing their growth to be inhibited or over-proliferated, destroying the structure and function of aquatic ecosystems.
    As for human health, inhalation through the respiratory tract can irritate the mucosa of the respiratory tract, make people cough, asthma, and even cause respiratory inflammation. If it is exposed to the skin, it may cause skin allergies, itching, redness and swelling. It is more dangerous to take it by mistake, or damage the human digestive system, causing nausea, vomiting, and abdominal pain. Long-term exposure to this environment, or involving the human nervous system and immune system, can reduce the body's resistance and increase the risk of disease.
    Therefore, the use and treatment of 6-methylpyridine-3-formonitrile should be handled with caution and strict regulations must be followed to prevent it from causing unbearable damage to the environment and human health.