2 Butyl 6 Butylamino 1h Benzo De Isoquinoline 1 3 2h Dione
quinoline thiophene imidazole thiazole

2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione

Taiy Chemical

    Specifications

    HS Code

    393802

    Chemical Formula C23H28N2O2
    Physical State Solid (usually)
    Appearance Colorless to pale - yellow solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like chloroform, dichloromethane
    Melting Point Specific value would require experimental determination
    Boiling Point Estimated based on similar compounds, requires experimental verification
    Density Value needs experimental measurement
    Pka Related to its acidic or basic functional groups, specific value via experiment

    As an accredited 2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615365036030 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365036030

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione in China?
    As a trusted 2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2-butyl-6-(butylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione 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 chemical structure of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione?
    This is an investigation into the chemical structure of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione. This compound is based on the benzo [de] isoquinoline parent nucleus, and the atoms on it are connected to form bonds in a specific order.
    Looking at its structure, the 1H-benzo [de] isoquinoline-1,3 (2H) -dione part is the skeleton of the core. Among them, the benzene ring is fused with the isoquinoline ring, which has a specific conjugate system. This conjugate structure has a profound impact on the physical and chemical properties of the compound. The presence of carbonyl groups at the 1st and 3rd positions gives this compound specific reactivity and can participate in many reactions such as nucleophilic addition.
    In addition, the 2nd position is connected with butyl (-C H), and butyl is alkyl, which has a power supply effect, which can affect the electron cloud density distribution of the benzisoquinoline ring, and then affect its reactivity and physical properties, such as solubility, boiling point, etc.
    And the 6-position butylamino (-NH-C H), the amino nitrogen atom has a lone pair electron, which can be used as both a hydrogen bond donor and a hydrogen bond receptor. It plays an important role in the interaction between molecules, or affects the crystal structure and biological activity of compounds. The existence of butyl also contributes to its spatial structure and hydrophobicity.
    In summary, the chemical structure of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione determines its unique chemical and physical properties by the interaction of each partial group.
    What are the main uses of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione?
    2 - butyl - 6- (butylamino) - 1H - benzo [de] isoquinoline - 1,3 (2H) - dione, this is an organic compound, commonly known as scopolamine butylbromide. It has a wide range of uses and is of critical significance in many fields.
    In the field of medicine, this compound is an important active ingredient. First, it has significant efficacy in antispasmodic. It can effectively relieve smooth muscle spasms such as gastrointestinal tract, biliary tract and urinary tract, and relieve pain caused by spasms. For patients with colic, after administration, intestinal smooth muscle spasms can be relieved, and pain symptoms can also be relieved. Second, it can effectively inhibit gland secretion. When applied before surgery, it can reduce the secretion of salivary glands and respiratory glands, create good conditions for surgery, and avoid excessive secretions during surgery that affect the operation or cause respiratory obstruction. Third, it also makes a difference in improving the level of microcirculation. It can expand microvessels and improve microcirculation perfusion, which is of positive significance for the treatment of certain microcirculation disorders-related diseases.
    In the chemical field, as a special organic compound, it can act as an intermediate for organic synthesis. With the help of specific chemical reactions, more complex organic molecular structures can be constructed on this basis, which can be used to prepare other materials or compounds with special properties, providing key raw material support for the innovative research and development of chemical products.
    In the field of scientific research, it is often used as a research object due to its unique chemical structure and properties. Through in-depth research on it, researchers explore its chemical reaction mechanism, pharmacological action mechanism, etc., to help promote the development of organic chemistry, medicinal chemistry and other disciplines, and contribute to the improvement of the knowledge system in related fields.
    What is the synthesis method of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione?
    To prepare 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione, the method is as follows:
    First, select a suitable starting material, usually starting with a benzoic acid derivative with a specific substituent and a nitrogen-containing heterocyclic compound. First, the benzoic acid derivative is treated with a specific reagent to make it undergo a specific transformation, such as reacting with an acylating reagent to convert the carboxyl group into an active acyl structure. This step can enhance its reactivity and facilitate subsequent reactions.
    Then, the nitrogen-containing heterocyclic compound participates in the reaction. Under suitable reaction conditions, such as in a specific solvent, adjust the temperature and pH to cause nucleophilic substitution or condensation of the two. This process requires fine control of the reaction conditions. Due to high or low temperature and improper pH, side reactions may occur, affecting the purity and yield of the product.
    During the reaction process, suitable monitoring methods, such as thin-layer chromatography (TLC), are required to clarify the progress of the reaction, determine the consumption of starting materials and the formation of the product. When the reaction reaches the desired level, the reaction is terminated.
    Subsequently, the reaction mixture is post-treated. Often by extraction, washing, drying and other operations to remove impurities and separate the target product. During extraction, the appropriate extractant is selected to achieve preliminary separation according to the solubility of the product and impurities in different solvents. Washing can remove residual reagents and by-products, and drying removes water to obtain a purer crude product.
    Finally, the crude product is purified by column chromatography or recrystallization. The column chromatography method separates the product and the impurity according to the difference in the partition coefficient between the stationary phase and the mobile phase; the recrystallization method uses the difference in the solubility of the product and the impurity in a specific solvent with temperature to make the product crystallize and precipitate, and achieve the purpose of purification. The final product is 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione with high purity.
    What are the physical properties of 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione?
    2-Butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione, this is an organic compound. It has some unique physical properties.
    Looking at its properties, it is mostly solid at room temperature and pressure. Due to the molecular structure containing multiple aromatic rings and polar groups, the intermolecular force is strong, resulting in a solid state.
    When it comes to the melting point, due to the complexity of its molecular structure and the intermolecular force, the melting point is relatively high. However, the exact melting point value will vary depending on the purity of the sample and the measurement conditions. Generally speaking, it may be between 150 ° C and 200 ° C.
    In terms of solubility, this compound is insoluble in water. Although it contains some polar groups in the molecule, the aromatic ring and the long-chain alkyl group account for a large proportion, and the whole is non-polar or weakly polar. It is difficult to form an effective interaction with water molecules, so the solubility in water is very small. However, in organic solvents, such as dichloromethane, chloroform, acetone, etc., it has a certain solubility. This is because these organic solvents and the compound molecules can form a similar and soluble effect, so that the molecules can be dispersed in the solvent.
    Furthermore, the compound has certain optical properties due to the presence of a conjugated system in the molecule. Under the irradiation of specific wavelengths of light, absorption phenomena may occur, which can be detected by ultraviolet-visible spectroscopy. This property may make it have potential applications in the field of optical materials or analytical detection.
    In addition, due to the active checking points such as nitrogen atoms in the molecule, or chemical reactions with other substances, which in turn affect its physical properties, such as the formation of new compounds after the reaction, its melting point, solubility and other properties may be changed.
    How safe is 2-butyl-6- (butylamino) -1H-benzo [de] isoquinoline-1,3 (2H) -dione?
    2 - butyl - 6- (butylamino) - 1H - benzo [de] isoquinoline - 1,3 (2H) - dione, this is an organic compound. Its safety needs to be investigated in detail from many aspects.
    Looking at its chemical structure, this compound contains specific functional groups, which may affect its chemical activity and stability. For example, the presence of butyl and butylamino groups may increase the hydrophobicity of the molecule, which also affects its behavior in the body and external environment.
    Toxicological studies are essential to clarify its safety. In terms of acute toxicity, if ingested or exposed to this compound, it may cause immediate adverse reactions in the body. For example, in animal experiments, high-dose exposure may cause acute symptoms such as organ damage and behavioral abnormalities. Chronic toxicity cannot be ignored. Long-term low-dose exposure may slowly damage body functions, such as affecting the reproductive system, immune system, or even carcinogenesis.
    Its environmental safety should not be underestimated. In the environment, the degradability of this compound is a key consideration. If it is difficult to degrade, or accumulates in the environment, it endangers the ecosystem. If it is in the aquatic environment, or affects the survival and reproduction of aquatic organisms, it is transmitted through the food chain, and ultimately affects human health.
    To accurately determine its safety, it is necessary to rely on experimental data and research results. It is necessary to conduct rigorous experiments to determine half lethal dose, genotoxicity, ecotoxicity and other indicators in order to obtain accurate safety information and provide a solid basis for its application and risk management.