Pyridine 5 Bromomethyl 2 Chloro
pyridine pyrrole pyrazine piperidine piperazine

Pyridine, 5-(bromomethyl)-2-chloro-

    Specifications

    HS Code

    917452

    Chemical Formula C6H5BrClN
    Molecular Weight 206.47
    Appearance Solid (predicted)
    Boiling Point 254.9°C at 760 mmHg (predicted)
    Melting Point 60 - 64°C
    Density 1.676 g/cm³ (predicted)
    Flash Point 107.9°C (predicted)
    Water Solubility Insoluble (predicted)
    Logp 3.21 (predicted)
    Pka 1.56±0.10 (predicted)

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    General Information
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    Frequently Asked Questions

    As a leading Pyridine, 5-(bromomethyl)-2-chloro- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of this product 5- (bromomethyl) -2-chloropyridine?
    This is about the chemical properties of (5- (hydroxymethyl) -2 -furanaldehyde). This substance, also known as furfural, has the structural characteristics of aldehyde groups and furan rings, so it presents many unique chemical properties.
    Bearing the brunt, because it contains aldehyde groups, it can carry out oxidation reactions. In case of strong oxidants such as potassium permanganate, aldehyde groups are easily oxidized to carboxylic groups to obtain products such as furfuric acid. In case of weak oxidants such as Torun reagent (silver ammonia solution), a silver mirror reaction can occur, the aldehyde group is oxidized, and metal silver is formed to adhere to the wall of the container, just like a silver mirror. This reaction is often used to test the aldehyde group. In case of Feilin reagent, the divalent copper ion can also be reduced to the red precipitation of cuprous oxide bricks, which is due to the reduction of the aldehyde group.
    Furthermore, due to the presence of aldehyde groups, an addition reaction can occur. For example, when catalyzed with alcohols in acids, acetals can be formed. This reaction is often used in organic synthesis as a means of protecting aldehyde groups. Addition with hydrocyanic acid can obtain α-hydroxynitriles, which can be used to increase carbon chains and expand molecular structures.
    In addition, the presence of the furan ring makes the substance aromatic and can undergo electrophilic substitution reactions. Because the furan ring is an electron-rich aromatic ring, the electron cloud density is higher, and the electrophilic reagents are easy to attack the position of the higher electron cloud density on the ring. Common electrophilic substitution reactions such as halogenation, nitrification, sulfonation, etc., the substitution position is mostly in the α-position, because the electron cloud density of the α-position is higher than that of the β-position, the reaction activity is stronger.
    At the same time, the furan ring of furfural has certain stability, but under certain conditions, such as strong acidity or high temperature, the ring may also open, triggering a series of complex reactions and generating different products, which is also of great significance in organic synthesis and chemical production.
    What fields are 5- (bromomethyl) -2-chloropyridine used in?
    (Pentyl) substances, and the field of their application.
    For technical reasons, pentyl groups are often used in chemical synthesis. For example, pentyl bromide and other pentane substitutions can be used as raw materials for chemical synthesis, which can be used to modify the molecular properties. In the chemical reaction, pentyl groups can be alkylated and reactive, and pentyl groups can be introduced into specific compounds to improve their chemical properties and physical properties. This is of great value in the synthesis of materials and materials science. For example, in the research of some new materials, by introducing pentyl groups, the solubility and melting properties of materials can be improved to meet different technical requirements.
    In the field, compounds containing pentyl groups also have their uses. Some of the molecules contain pentyl groups, the presence of pentyl groups may affect the binding ability of the target of the compound, and the ability of the compound to be replaced in the future. For example, for some painkillers, the reasonable repair of pentyl groups can improve the fat solubility of the compound, making it easier to penetrate the biofilm, thus improving the bioavailability of the compound and increasing the efficiency.
    Furthermore, in the fragrance industry, pentyl compounds can be used as fragrance components. The special taste given by pentyl groups can add special fragrance to the fragrance. In some natural fragrances or synthetic fragrances, the presence of pentyl groups can make the fragrance more rich and rich, and can be widely used in perfumes, food additives, etc., to improve the fragrance of the product.
    Therefore, (pentyl) has demonstrated its important application value in many fields such as engineering, engineering, and fragrance, and has promoted the development of new products in various fields.
    What are the synthesis methods of 5- (bromomethyl) -2-chloropyridine?
    (5 - (hydroxymethyl) -2 -furanal), also known as furfural, its synthesis method is as follows:
    In the ancient method, agricultural and sideline products were often used as sources, such as corn cobs, bagasse, rice husks, etc. Rich in polypentosaccharides. It is co-heated with dilute acids, and the polypentosaccharides are first hydrolyzed into pentosaccharides, which are then dehydrated and cyclized to produce furfural. The process is just like changing things, following the laws of nature. As described in "Tiangong Kaiwu", all kinds of processes are based on physical properties. Among them, acid is the medium for change, heat is the force for change, and the two complement each other to transform the raw materials in sequence.
    Today's methods are based on biomass refining technology. Under specific reaction conditions, the power of high-efficiency catalysts is used to promote the conversion of hemicellulose and other components into furfural. This catalyst is like a craftsman, accurately guiding the reaction direction and improving the output of furfural. And the control of reaction conditions, such as temperature and pressure, are all fine and meticulous to achieve the best environment. This is also like the ancient good work, with a delicate grasp of the temperature and scale.
    There are also those who use the chemical synthesis path, starting from the basic chemical raw materials, and constructing the structure of furfural through multiple reactions. Although the steps are complicated, they can be adjusted on demand, and the product purity is also high. Each step of the reaction is like a craftsman, following the rules, carefully constructing the shape of the molecule.
    The method of synthesis, whether ancient or modern, follows the principle of material change, using manpower to guide material properties, seeking efficient and high-quality output, just like ancient man-made things, perfect, in order to apply the obtained things to the world.
    What is the market price of 5- (bromomethyl) -2-chloropyridine?
    (Looking at the present, the value of goods in the market often varies according to supply and demand and the current situation. As for the market of (hydroxymethyl) 2O ether, its price follows this principle.)
    (hydroxymethyl) 2O ether is widely used in the chemical industry. Its market price is mainly based on supply and demand. If there are many people who need it and it is widely used, such as in medicine and materials industries, their demand is prosperous, and if the supply is not enough, the price will increase; on the contrary, if there is less demand and more supply, the price will drop.
    The current situation is also a major factor. The regulations of the government, if the order of environmental protection, and the reform of taxes, can all affect its production and sales. Under strict regulations, the producer's fee increases, and its price may rise. The situation of the world, if the change of energy and the state of trade, also has an impact. Energy prices rise, the cost of its production rises, and the price also follows; trade is blocked, circulation is hindered, and prices fluctuate.
    In the past, the chemical industry was prosperous, and (hydroxymethyl) 2O ether needed more, and the price rose steadily. After new technologies were introduced, the yield increased, the supply gradually increased, and the price fell slightly. At present, environmental protection is becoming stricter, producers need to improve quality from regulations, and costs increase, causing prices to rise again.
    However, the market is unstable, and the price is also difficult to determine. Industry operators often observe changes in time, analyze supply and demand, and measure government orders to measure the trend of their prices and seek business benefits. Although the price of (hydroxymethyl) 2O ether has risen today, it is difficult to predict the value in the future due to changes in new production methods and needs. Only by responding to the situation can we be undefeated in the market.
    What are the storage conditions for 5- (bromomethyl) -2-chloropyridine?
    The storage conditions of (penta- (hydroxymethyl) -2-furanaldehyde) should be stored in a cool place away from light, and the container must be kept airtight.
    This substance is quite sensitive to light, and light can easily cause its chemical reaction, which in turn affects its quality and performance. Therefore, it needs to be stored in a dark place to prevent direct light. Furthermore, it may also react with oxygen and other components in the air, or deteriorate due to absorption of moisture in the air. Therefore, it is crucial to keep the container airtight, which can effectively reduce contact with air and avoid such adverse changes.
    At the same time, the temperature should not be ignored. It should be stored in a place with a relatively stable and low temperature. High temperature may accelerate its decomposition or other chemical reactions. Only under such storage conditions can the chemical stability and quality of (penta- (hydroxymethyl) -2-furanaldehyde) be maintained to the greatest extent, so that it can play its due effectiveness in subsequent use.