Isoquinoline 6 7 Dimethoxy 1 Veratryl Hydrochloride
quinoline thiophene imidazole thiazole

Isoquinoline, 6,7-dimethoxy-1-veratryl-, hydrochloride

Taiy Chemical

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    420916

    Chemical Name Isoquinoline, 6,7-dimethoxy-1-veratryl-, hydrochloride

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    Frequently Asked Questions

    As a leading Isoquinoline, 6,7-dimethoxy-1-veratryl-, hydrochloride 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 Isoquinoline, 6, 7-dimethoxy-1-veratryl-, hydrochloride
    The name of this compound is "6,7-dimethoxy-1-veratrol isoquinoline hydrochloride". In its chemical structure, isoquinoline is the parent nucleus and is a class of nitrogen-containing heterocyclic organic compounds. The 6 and 7 positions of isoquinoline are connected to methoxy (-OCH), and the 1 position is connected to veratrol. Veratrol usually refers to 3,4-dimethoxybenzyl, that is, benzyl (phenyl) has methoxy groups in the 3 and 4 positions of the phenyl ring. The whole compound exists in the form of hydrochloride, which means that the nitrogen atom binds to a proton (H < unk >) and forms a salt with the chloride ion (Cl). This structure endows the compound with specific physical and chemical properties and potential biological activities, which are often studied in the fields of organic synthesis and medicinal chemistry, and can be used as synthetic intermediates or lead compounds with specific physiological activities.
    What are the physical properties of Isoquinoline, 6, 7-dimethoxy-1-veratryl-, hydrochloride
    6,7-Dimethoxy-1-veratrol isoquinoline hydrochloride, this is an organic compound with specific physical properties. Its color state is often white to light yellow crystalline powder, which is easy to identify. It can be used as a preliminary basis for judgment when observing and treating related fields such as pharmaceuticals and chemical raw materials.
    In terms of solubility, it has a certain solubility in common organic solvents such as methanol and ethanol. Methanol and ethanol are widely used organic solvents. The solubility characteristics of the compound make it possible to select suitable solvents and optimize the process in the preparation of solutions, extraction, separation and reaction operations. For example, in the post-treatment step of chemical synthesis, its solubility in ethanol can be used for recrystallization to purify the product. The melting point of
    is of great significance for identification and quality control. After experimental determination, its melting point is in a specific range, and this value is a key indicator for judging the purity of the compound. If the melting point deviates from the normal range, or implies that it contains impurities, further purification is required. In production and research, melting point determination is a routine quality inspection method to ensure that the product meets the standards.
    Stability is also an important property. Under normal storage conditions, the compound is relatively stable, but under extreme conditions such as strong acid, strong base or high temperature, the structure may change. If in a high temperature environment, the vibration of chemical bonds in the molecule intensifies, which may trigger decomposition or rearrangement reactions; when strong acid and strong base exist, they may react with the active check point in the molecule and change the chemical structure. Therefore, when storing and using, it is necessary to avoid such extreme conditions to ensure its quality and performance.
    What is the use of Isoquinoline, 6, 7-dimethoxy-1-veratryl-, hydrochloride
    "Tiangong Kaiwu" was written by Song Yingxing in the Ming Dynasty, and the book recorded many processes and technologies in detail. However, at that time, the knowledge of chemical synthesis of drugs was still lacking, so it was impossible to discuss the use of "6,7-dimethoxy-1-veratrol isoquinoline hydrochloride" in the classical style of "Tiangong Kaiwu". Today, it is described in the style of ancient Chinese as follows:
    6,7-dimethoxy-1-veratrol isoquinoline hydrochloride, which is made by modern chemistry. Its uses are mostly involved in the field of medical research. In pharmaceutical research and development, or as a potential active ingredient, its impact on the physiological and pathological processes of the body can be explored, hoping to find a cure and a cure. In scientific research, it is often used as a research tool to help scientists investigate cellular and molecular mechanisms and gain insight into the mysteries of life. It can also be used to synthesize more complex compounds, expand the variety of chemical substances, and pave the way for new drug creation and material research and development. However, this material has specific chemical properties and activities, and it needs to be used in accordance with scientific norms and carefully to ensure safety and achieve the expected efficacy.
    What is the synthesis method of Isoquinoline, 6, 7-dimethoxy-1-veratryl-, hydrochloride
    The synthesis of 6,7-dimethoxy-1-veratrol isoquinoline hydrochloride is an important research in the field of organic synthesis. The synthesis path is often determined by the basic reaction principles of organic chemistry and existing synthesis experience.
    First, suitable starting materials can be found. Or choose a compound with isoquinoline parent nucleus, or choose a small molecule that can construct an isoquinoline structure through a series of reactions. For example, phenethylamine compounds with appropriate substituents and aldehyde derivatives of veratrol are used as starting materials. The two can be condensed and cyclized under the condition of acid catalysis by Pictet-Spengler reaction to form isoquinoline structures. In this step, attention should be paid to the reaction temperature, catalyst type and dosage, because these factors have a significant impact on the yield and selectivity of the reaction. Usually, mild heating and an appropriate amount of Lewis acid catalysis, such as aluminum trichloride, can make the reaction proceed better.
    Second, if the isoquinoline intermediate generated by the reaction needs to introduce methoxy groups, it can be synthesized by Williamson ether. With appropriate halogenated hydrocarbons (such as iodomethane) and hydroxyl-containing isoquinoline intermediates, under the action of bases (such as potassium carbonate), nucleophilic substitution occurs, thereby introducing methoxy groups. This step requires attention to the choice of reaction solvent. Polar aprotic solvents such as N, N-dimethylformamide (DMF) can often improve the reaction rate and yield.
    Furthermore, after the required substituents are introduced to obtain the target isoquinoline compound, to obtain hydrochloride, the compound can be dissolved in a suitable organic solvent (such as ether or dichloromethane), passed into hydrogen chloride gas, or dropwise added alcohol solution of hydrogen chloride to form a salt with hydrogen chloride, and then precipitate the target product 6,7-dimethoxy-1-veratrol isoquinoline hydrochloride. < Br >
    However, during the synthesis process, it is necessary to carefully control the reaction conditions of each step, including temperature, time, material ratio, etc. After each step of the reaction, appropriate separation and purification methods, such as column chromatography, recrystallization, etc., are required to obtain high-purity intermediates and final products to ensure the success of synthesis and product quality.
    What are the safety precautions for Isoquinoline, 6, 7-dimethoxy-1-veratryl-, hydrochloride
    6,7-Dimethoxy-1-veratrol isoquinoline hydrochloride, this is a special chemical. Regarding its safety precautions, it should be detailed with ancient warnings.
    First of all, this chemical may be potentially toxic. When in contact, do not let the skin come into contact with it. If you accidentally touch it, rinse it with plenty of water as soon as possible, and then seek medical attention. This is a life-saving move, and it must not be slack.
    Furthermore, the smell should also be paid attention to. Its volatile gas may enter the lungs and damage the body. Therefore, when operating in a well-ventilated place, it is advisable to wear a gas mask if necessary to protect breathing.
    In addition, the method of preservation is also exquisite. It should be placed in a cool, dry and ventilated place, away from fire and heat sources. Because of its flammability, a little carelessness will lead to the disaster of blending.
    When taking it, be sure to measure it with accurate utensils, and do not do it at will. More is wasteful and dangerous, and less is not as effective as expected.
    In addition, if there is any waste of this object, it must not be discarded at will. When in accordance with relevant laws and regulations, it should be properly disposed of to avoid polluting the environment and harming all living beings.
    In summary, handling 6,7-dimethoxy-1-veratrol isoquinoline hydrochloride requires awe and strict adherence to procedures to ensure safety.