2 Chloro N4 2 Methypropyl 3 4 Quinolinediamine
quinoline thiophene imidazole thiazole

2-Chloro-N4-(2-methypropyl)-3,4-quinolinediamine

Taiy Chemical

    Specifications

    HS Code

    742501

    Chemical Formula C14H18ClN3
    Molecular Weight 263.77
    Appearance Typically a solid
    Physical State At Room Temperature Solid
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Melting Point Data may vary, needs specific research
    Boiling Point Data may vary, needs specific research
    Pka Relevant to its amine functional groups, data may vary

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    General Information
    Where to Buy 2-Chloro-N4-(2-methypropyl)-3,4-quinolinediamine in China?
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    Frequently Asked Questions

    As a leading 2-Chloro-N4-(2-methypropyl)-3,4-quinolinediamine 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 2-Chloro-N4- (2-methypropyl) -3,4-quinolinediamine?
    2-Chloro-N4- (2-methylpropyl) -3,4-quinolinediamine, which has a wide range of uses. In the field of medicine, it may be an important intermediate for drug synthesis. The guinequinoline structure is common in many drug molecules. By chemical modification and modification of 2-chloro-N4- (2-methylpropyl) -3,4-quinolinediamine, drugs with specific pharmacological activities can be prepared, such as antibacterial and anti-tumor drugs.
    In the field of materials science, it also has potential uses. Quinoline derivatives often exhibit unique optical and electrical properties. On the basis of this compound, through rational molecular design and synthesis, excellent photoelectric materials may be prepared, such as materials used in organic Light Emitting Diode (OLED), solar cells and other fields.
    Furthermore, in agricultural chemistry, it may be used as a raw material for pesticide synthesis. Some compounds containing quinoline structure have good control effect on crop diseases and pests, and 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine can be properly converted, or high-efficiency, low-toxicity and environmentally friendly pesticides can be developed.
    What are the chemical properties of 2-Chloro-N4- (2-methypropyl) -3,4-quinolinediamine
    2-Chloro-N4- (2-methylpropyl) -3,4-quinoline diamine, this is an organic compound. Its chemical properties are rich and diverse, let me tell them one by one.
    First talk about its physical properties. Under normal conditions, it may be a solid state. As for the color, it may vary with purity. The pure product may be white or nearly white powder. Looking at its solubility, it may have a certain solubility in organic solvents, such as ethanol and dichloromethane. However, in water, its molecular structure contains hydrophobic quinoline rings and alkyl groups, so its solubility is poor.
    When it comes to chemical properties, the first one is the reaction of its amine groups. Amines are basically alkaline and can be neutralized with acids to form corresponding salts. In the case of inorganic acids such as hydrochloric acid and sulfuric acid, stable salts can be formed, which is of great practical value in the process of separation, purification and preparation. At the same time, amine groups can also participate in nucleophilic substitution reactions. If they encounter suitable halogenated hydrocarbons, further alkylation reactions can occur, resulting in more complex molecular structures.
    Furthermore, its chlorine atoms are also active. As a good leaving group, chlorine atoms can undergo nucleophilic substitution reactions under basic conditions or under the action of nucleophiles. With the action of sodium alcohol and amine nucleophiles, chlorine atoms can be replaced to form new compounds. This is a common strategy for building new chemical bonds in organic synthesis.
    The presence of quinoline ring endows the compound with unique chemical properties. Quinoline ring has aromatic properties and can undergo aromatic electrophilic substitution reaction. If it interacts with mixed acids such as nitric acid and sulfuric acid, nitro and other substituents can be introduced into the quinoline ring. And the compound may have certain redox properties. Under specific conditions, the quinoline ring can be oxidized to form various oxidation products.
    And because its structure contains different functional groups, each functional group may interact with each other. Amine groups and chlorine atoms, quinoline rings, or through electronic effects and spatial effects, affect each other's reaction activities, making their chemical properties more complex and interesting. The chemical properties of this compound lay an important foundation for the research and application in the fields of organic synthesis and medicinal chemistry.
    What is the production process of 2-Chloro-N4- (2-methypropyl) -3,4-quinolinediamine?
    The production process of 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine is the key to the field of fine chemical synthesis. The preparation process is like a delicate chemical "dance" that requires many steps and precise control.
    At the beginning, specific quinoline derivatives are often used as raw materials. This raw material is carefully selected, and its structural characteristics play a decisive role in the subsequent reaction direction. Then, in the chlorination step, chlorine atoms need to be introduced onto the quinoline structure. This process is like being carved on a precision instrument, and the reaction conditions need to be precisely adjusted. Temperature, reaction time, and the amount of chlorination reagent are all key factors. The choice of chlorination reagents is also very particular, and different reagents will have a significant impact on the reaction rate and product purity.
    After the successful introduction of chlorine atoms, the key step of N4- (2-methylpropyl) substitution is entered. It is necessary to select a suitable reagent containing 2-methylpropyl and use the power of a catalyst to cause it to react with chlorinated quinoline derivatives. This reaction is like building a chemical "building block". The catalyst is like a magical "magic wand", accelerating the reaction process and ensuring that 2-methylpropyl is accurately connected to the target location.
    Separation and purification steps are also indispensable throughout the production process. The reaction mixture often contains many impurities. It is necessary to separate the target product 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine precisely by means of distillation, crystallization, column chromatography, etc., to improve its purity to meet the needs of different fields. This process is like panning for gold in the sand, and only fine operation can obtain a pure product. Each step is closely connected, interlocking, and a slight difference may affect the quality and yield of the product, which shows the delicacy and complexity of this production process.
    What is the price range of 2-Chloro-N4- (2-methypropyl) -3,4-quinolinediamine in the market?
    It is difficult to determine the price range of 2-chloro-N4- (2-methylpropyl) -3,4-quinolinediamine in the market. Due to various reasons, its price fluctuates.
    First, the supply and demand situation of this product has a great impact on the price. If there are many people who want it, and the supply is small, the price will increase; conversely, if the supply exceeds the demand, the price will decline. If the demand for it surges in various industries, and the producer fails to expand production in time to respond, the price will rise.
    Second, the price of raw materials also affects its price. The preparation of this material requires specific raw materials. If the price of raw materials increases and the cost of the manufacturer increases, in order to ensure profits, the price of this product must be raised. For example, the price of raw materials is high due to scarcity of resources or production changes, and the price of 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine also rises.
    Third, whether the preparation process is simple and advanced or not is related to the cost, which in turn affects the price. If the process is complicated, many steps and expensive equipment are required, and the cost must be high and the price is not cheap; but the new and excellent process can reduce the cost and make the price more competitive.
    Fourth, the market competition situation is also the key. When there are many market producers, competing for profits from each other, in order to occupy a share, or will reduce prices for promotion; and if the market is monopolized, the producers can control the price.
    Overall, the price of 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine can range from ten yuan per single digit to hundreds of yuan. The specific price must be carefully studied according to the current market conditions before it can be clarified.
    What are the relevant safety precautions for 2-Chloro-N4- (2-methypropyl) -3,4-quinolinediamine?
    2-Chloro-N4- (2-methylpropyl) -3,4-quinolinediamine is an organic compound. Regarding the safety precautions of this substance, the following numbers should be paid attention to in detail:
    First, toxicity. This compound may be toxic, contact with the human body, or through skin penetration, mouth and nose inhalation, accidental ingestion, etc., invade the body and damage health. If the skin touches it, it may cause allergies, redness, and itching; if the dust or volatile gas is inhaled, it can cause respiratory irritation, such as coughing, asthma, breathing difficulties, etc.; if taken accidentally, it will harm the digestive system, including nausea, vomiting, abdominal pain, etc., and even life-threatening. Therefore, when operating, be sure to strictly abide by the operating procedures and take good protection.
    Second, the danger of combustion and explosion. This object may be flammable under certain conditions. In case of open fire, hot topic, or cause combustion. If it is in a limited space, it will burn violently and there is a risk of explosion. Store and use it away from fire and heat sources, and maintain good ventilation to prevent it from accumulating and forming an explosive environment. < Br >
    Third, environmental impact. If this compound flows into the environment, it may cause harm to the ecology. It may have adverse effects such as inhibition of growth and teratogenicity on aquatic organisms, soil microorganisms, etc., and destroy the ecological balance. During use, do not dump waste containing this compound at will, and it must be properly disposed of according to environmental protection requirements.
    Fourth, storage attention. It should be stored in a cool, dry and well-ventilated place, away from oxidants, acids and other chemicals to prevent reactions. The packaging must be sealed to prevent its leakage. At the same time, the storage area should be equipped with suitable containment materials to deal with possible leakage.
    Fifth, operation protection. When operating, it is necessary to wear appropriate protective equipment, such as protective gloves, choose chemical corrosion-resistant materials to ensure comprehensive hand protection; wear protective glasses to protect your eyes from splash damage; if necessary, also need to be equipped with a gas mask to prevent inhalation of harmful substances. After the operation, wash the contact area in time and change clothes.
    In short, use 2-chloro-N4- (2-methylpropyl) -3,4-quinoline diamine, when there is a clear understanding of its potential hazards, strictly abide by safety regulations to ensure that personnel safety and the environment are not damaged.