6 Quinolinecarboxylic Acid Methyl Ester
quinoline thiophene imidazole thiazole

6-Quinolinecarboxylic acid, methyl ester

Taiy Chemical

    Specifications

    HS Code

    396570

    Chemical Formula C11H9NO2
    Molar Mass 187.195 g/mol
    Appearance Solid
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

    As a leading 6-Quinolinecarboxylic acid, methyl ester 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 main use of methyl 6-quinoline carboxylate?
    Ethyl 6-pentenoheptanoate is also an organic compound. Its main uses are quite extensive.
    In the field of fragrances, ethyl 6-pentenoheptanoate can be used as a fragrance component. Because of its unique smell, it can add a unique aroma to various fragrance formulations. Or it can be used to prepare a variety of fragrances such as floral and fruity. In the preparation of daily necessities such as perfumes, air fresheners, and detergents, it can increase the richness and layering of the aroma of the product, making the aroma more attractive.
    In the field of food additives, this compound can be used as a edible fragrance. It can give food a unique flavor. For example, when making candies, beverages, baked goods, etc., an appropriate amount of ethyl 6-pentenheptanoate can simulate a specific fruity aroma or other attractive flavors, improve the flavor quality of food, and enhance consumer appetite.
    In the field of organic synthesis, ethyl 6-pentenheptanoate also has important uses. Because its molecular structure contains active functional groups such as alkenyl and ester groups, it can be used as an intermediate in organic synthesis. Through various organic reactions, such as addition reactions, substitution reactions, etc., it can be converted into other more complex organic compounds, providing key starting materials or intermediates for drug synthesis, materials science and other fields, which is of great significance for the development and production of new compounds.
    What are the physical properties of methyl 6-quinoline carboxylate?
    6-Ethyl pentenoate is an organic compound with unique physical properties, detailed as follows:
    1. ** Properties **: Usually in the state of colorless to light yellow liquid, it can be seen at room temperature and pressure. Its flowing posture is clear and transparent, and there are no obvious impurities. This form makes it easy to handle and operate in many chemical reactions and industrial applications.
    2. ** Odor **: It exudes a faint and fruity aroma, similar to the fragrance emitted by some ripe fruits. This odor characteristic makes it a place in the fragrance industry and can be used as a raw material for blending specific fragrances.
    3. ** Boiling point **: Its boiling point is about 185-187 ° C. The boiling point value shows that under standard atmospheric pressure, the temperature needs to be increased to this range before ethyl 6-pentenoate can be converted from liquid to gaseous. This boiling point characteristic is crucial in the separation and purification of the compound. With the help of distillation and other means, pure ethyl 6-pentenoate can be accurately obtained from the mixture according to its boiling point difference.
    4. ** Melting point **: The melting point is about -70 ° C. This means that at temperatures below this temperature, ethyl 6-pentenoate will solidify from liquid to solid. The low melting point allows the compound to maintain a liquid state at most conventional ambient temperatures, making it convenient for storage and transportation.
    5. ** Solubility **: It is insoluble in water, but it can be miscible with organic solvents such as ethanol and ether in any ratio. The property of insolubility in water is related to the force between water molecules and ethyl 6-pentenoate molecules, and its molecular structure makes it difficult for it to attract and fuse with water molecules. The good miscibility with organic solvents provides convenience for its use in organic synthesis and other fields, and can realize dissolution and reaction operations with the help of organic solvents.
    6. ** Density **: The density is slightly smaller than that of water, about 0.91 g/cm ³. This density characteristic makes it float above the water surface when mixed with water, and can be used for some separation operations based on density differences. In specific chemical production processes, this property can effectively achieve the initial separation of different substances.
    What is the chemical synthesis method of methyl 6-quinoline carboxylate?
    To prepare ethyl 6-pentenoate, the method is as follows:
    First take pentenoic acid, co-place it in a reaction kettle with ethanol, and add an appropriate amount of concentrated sulfuric acid as a catalyst. For concentrated sulfuric acid, this reaction can promote its esterification, and its performance is active, which can increase the reaction rate. Control the temperature to a suitable degree, about 70-80 degrees Celsius. Temperature control is crucial. If it is too low, the reaction will be slow, and if it is too high, it may cause side reactions to produce and damage the purity of the product.
    At this temperature, pentenoic acid and ethanol are esterified, and the two molecules are dehydrated and condensed. The carboxyl group in pentenoic acid interacts with the hydroxyl group of ethanol to remove one molecule of water to form ethyl 6-pentenoate. The reaction formula is roughly as follows: pentenoic acid + ethanol $\ stackrel {concentrated sulfuric acid, 70 - 80 ℃}{=\!=\!=}$ ethyl 6-pentenoate + water.
    After the reaction is completed, the product is mixed with unreacted raw materials, catalysts and impurities such as water. Wash it with a saturated sodium carbonate solution first. Sodium carbonate can be neutralized with sulfuric acid and can remove unreacted pentenoic acid. Because pentenoic acid can react with sodium carbonate to form a soluble salt, ethyl 6-pentenoate is insoluble and layered to facilitate separation.
    Then separate the liquid with a separation funnel to take the organic phase. The organic phase still contains a small amount of water. In addition to a desiccant such as anhydrous magnesium sulfate, let it stand for a while to allow the water to be absorbed by the desiccant.
    Finally, by distillation, pure ethyl 6-pentenoate is obtained. During distillation, the temperature is controlled near the boiling point of ethyl 6-pentenoate, and the fraction is collected to obtain the desired product.
    Although this process step is complicated, it is performed in sequence to obtain a relatively pure ethyl 6-pentenoate.
    What are the precautions for methyl 6-quinoline carboxylate during storage and transportation?
    6-Ethyl pentenoate, during storage and transportation, it is necessary to pay attention to many matters.
    When storing, the first choice of environment. It should be placed in a cool and ventilated warehouse, away from fires and heat sources. Because of its flammability, it is easy to cause combustion and explosion in case of open flames and hot topics. The temperature of the warehouse should be controlled within a suitable range to prevent excessive temperature from intensifying its volatilization or triggering other chemical reactions. In addition, it should be stored separately from oxidants, acids, bases, etc., and must not be mixed. Contact with these substances, or react violently, endangering safety.
    There are also many taboos during transportation. The transportation vehicle must be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. When driving, make sure that the container does not leak, collapse, fall or damage. During transportation, it should be protected from exposure to the sun, rain and high temperature. If it is transported in summer, it is advisable to drive in the morning and evening to avoid high temperature periods. And the trough (tank) car used during transportation should have a grounding chain, and holes can be set in the trough baffle to reduce shock and generate static electricity. When loading and unloading personnel operate, they need to load and unload lightly. It is strictly forbidden to drop, heavy pressure and friction to avoid material leakage caused by damage to the container.
    During transportation, it should also drive according to the specified route and do not stop in residential areas and densely populated areas. In the event of a leak or other accident, the personnel accompanying the vehicle should take emergency measures immediately, evacuate the surrounding people, call the police for assistance, and properly dispose of it according to the characteristics of the material to ensure the safety of personnel and the environment from pollution. In this way, it is necessary to ensure the safety of ethyl 6-pentenate during storage and transportation.
    Is methyl 6-quinoline carboxylate potentially harmful to the environment and human health?
    6-Ethyl pentenoate, which is hidden or potentially dangerous to the environment and human health.
    The properties of ethyl pentenoate, which are volatile, in the atmosphere, or interact with other chemicals, causing changes in atmospheric composition. If it is released in the environment or enters the human body through the respiratory tract. The human lungs, the function of the department of respiration, are the place for gas exchange. The gas of ethyl pentenoate enters the lungs, or stimulates the mucosa of the lungs, causing coughing and asthma. And the lungs direct the air, towards the veins, this harmful substance may flow around the body with qi and blood, damaging the viscera. < Br >
    And it is in the aquatic environment. If it flows into rivers, lakes and seas, aquatic organisms bear the brunt. The gills of fish are for respiration and excretion. Ethyl pentenoate enters the water or enters the fish body through the gills, affecting its respiration and metabolism. The growth of aquatic plants may also be harmed by it. The roots of plants draw nutrients from water, and ethyl pentenoate may interfere with their nutrient uptake and physiological metabolism, causing growth to be blocked or even withered.
    Furthermore, in the soil environment, if ethyl pentenoate penetrates into the soil, it may affect the structure and function of the soil microbial community. Soil microorganisms are crucial to soil fertility and material circulation. If it is affected, the ecological balance of the soil may be destroyed, which in turn endangers the growth of plants.
    Although the impact of ethyl pentenate on the environment and human health has not been observed at present, the potential danger cannot be ignored. Our generation should carefully observe it, study its nature, investigate its harm, and implement preventive measures to protect the environment and human well-being.