2 4 Dibromothiophene
quinoline thiophene imidazole thiazole

2,4-Dibromothiophene

Taiy Chemical

    Specifications

    HS Code

    332408

    Chemical Formula C4H2Br2S
    Molar Mass 255.93 g/mol
    Appearance Solid
    Melting Point 72 - 76 °C
    Boiling Point 244 - 245 °C
    Density N/A
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents
    Odor N/A
    Flash Point N/A
    Cas Number 638-08-4

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    Frequently Asked Questions

    As a leading 2,4-Dibromothiophene 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 main uses of 2,4-dibromothiophene?
    2% 2C4-dibromopentane is also an organic compound. Its main use is quite wide. In the context of "Tiangong Kaiwu", although it was not called by modern chemical names at that time, it can also be said in terms of the consumption of chemical substances.
    In the field of organic synthesis, 2% 2C4-dibromopentane is often an important raw material. Because of its molecular structure, it contains dibromine atoms. This dibromine atom has active chemical properties and can introduce different functional groups through many chemical reactions, such as nucleophilic substitution reactions, and interact with various nucleophilic reagents, thereby forming more complex organic molecular structures. This is especially crucial in the preparation of drugs, fragrances and other fine chemicals with special structures.
    In drug synthesis, specific groups can be introduced through a multi-step reaction starting with 2% 2C4-dibromopentane to meet the requirements of combining drug molecules with targets. For example, by reacting with reagents containing nucleophilic groups such as nitrogen and oxygen, a compound skeleton with specific pharmacological activities can be constructed.
    Fragrance synthesis is also commonly used. Because it can participate in the reaction to generate compounds with special aroma structures. Or through a series of transformations, a unique combination of carbon chain structures and functional groups can be formed to give fragrances a unique flavor.
    In addition, in the field of materials science, 2% 2C4-dibromopentane may participate in the polymerization reaction. Its bromine atom can initiate polymerization under appropriate conditions, or act as a linking group to connect different monomers, so as to prepare polymer materials with special properties, such as improving the thermal stability and mechanical properties of materials.
    In summary, 2% 2C4-dibromopentane has important uses in many fields such as organic synthesis, drugs, fragrances and materials due to its unique structure. Although it is not detailed in "Tiangongkai", its wide range of uses and deep impact cannot be underestimated in today's scientific perspective.
    What are the physical properties of 2,4-dibromothiophene?
    2% 2C4-dibromopentane is an organic compound, and its physical properties are quite unique. Looking at its properties, at room temperature, it is mostly a colorless to light yellow transparent liquid, which is like smart water, but contains different qualities. Its smell is slightly irritating, just like a slightly pungent breeze, lingering in the sense of smell.
    When it comes to density, 2% 2C4-dibromopentane has a density greater than that of water. It is like a stable stone. When thrown into water, it will slowly sink. This property makes it unique in the separation of many mixtures. Its boiling point is about a certain range, which varies slightly due to specific experimental conditions and purity. It is roughly in a certain range. This boiling point makes it change from liquid to gaseous at a specific temperature, just like ice melts into water, and water sublimates into gas, following the law of material transformation.
    Furthermore, the solubility of 2% 2C4-dibromopentane cannot be ignored. It is insoluble in water, and the two are like incompatible strangers, distinct in the same container. However, it is soluble in a variety of organic solvents, such as ethanol, ether, etc., just like a wanderer returning home, it can blend with these organic solvents and integrate with each other. This solubility lays the foundation for its application in organic synthesis and other fields.
    In addition, the volatility of 2% 2C4-dibromopentane is relatively moderate, neither extremely volatile, such as the fleeting light smoke, nor difficult to evaporate, such as the stubborn heavy stone. Moderate volatility makes it necessary to follow specific specifications during storage and use to ensure the stability of its properties and the safety of use.
    Such physical properties make 2% 2C4-dibromopentane valuable and unique in many fields such as chemical industry and scientific research.
    What are the chemical properties of 2,4-dibromothiophene?
    2% 2C4-dibromopentane is also an organic compound. Its chemical properties are quite interesting, let me tell you in detail.
    In this compound, the presence of bromine atoms endows it with unique reactivity. Due to the strong electronegativity of bromine atoms, the carbon-bromine bond polarity in 2% 2C4-dibromopentane is quite large. This polarity makes the molecule vulnerable to attack by nucleophiles.
    When encountering nucleophiles, the carbon-bromine bond can be broken, and nucleophiles replace it. If co-heated with an aqueous solution of sodium hydroxide, hydroxy (-OH) can replace bromine atoms as nucleophiles to generate 2% 2C4-pentanediol. This is a typical example of a nucleophilic substitution reaction.
    Furthermore, 2% 2C4-dibromopentane can also be eliminated. When co-heated with an alcohol solution of potassium hydroxide, the bromine and hydrogen atoms on adjacent carbon atoms can be removed to form unsaturated olefins. During this reaction, the intramolecular chemical bonds are rearranged to form carbon-carbon double bonds, which is an important way to construct carbon-carbon unsaturated bonds in organic synthesis.
    In addition, due to the presence of two bromine atoms in the molecule, the reaction selectivity is also of concern. Under different reaction conditions, the position of nucleophilic attack may be different, or one of the bromine atoms is preferentially replaced, or both bromine atoms are replaced, depending on the reaction substrate structure, nucleophilic reagent activity and reaction conditions.
    From the above, 2% 2C4-dibromopentane plays an important role in organic chemical reactions due to the characteristics of bromine atoms. Its nucleophilic substitution and elimination reactions provide many possibilities for organic synthesis chemistry, which can be used to prepare a variety of organic compounds with specific structures and functions.
    What is the preparation method of 2,4-dibromothiophene?
    The preparation method of 2% 2C4-dibromopentane is as follows:
    To prepare 2% 2C4-dibromopentane, pentane can be taken as the starting material. In the pentane molecule, hydrogen atoms can be replaced by bromine atoms due to suitable reaction conditions. This preparation often requires the help of bromination reaction, and most of them are initiated by light or heating.
    Under light conditions, bromine molecules (Br ²) can be excited by light to cleave into bromine radicals (Br ·). The hydrogen atoms in pentane (C H -2) molecules will be captured by bromine radicals with different degrees of difficulty due to different chemical environments. There are three different types of hydrogen atoms in pentane, which are located on primary, secondary and tertiary carbon atoms. Generally speaking, secondary hydrogen atoms are more easily replaced by bromine atoms in the reaction due to their moderate activity to generate 2-bromopentane.
    After 2-bromopentane is formed, it can be reacted with bromine elemental substance under the same bromination conditions again. At this time, the hydrogen atom in the 2-bromopentane molecule can be attacked by bromine free radicals under light or heating. Due to the characteristics of the molecular structure of 2-bromopentane, under suitable conditions, the hydrogen atom at position 4 can be replaced by the bromine atom again, thereby obtaining 2% 2C4-dibromopentane.
    This reaction process requires attention to the precise control of the reaction conditions. Light intensity, temperature, and the proportion of reactants all have significant effects on the reaction process and product yield. If the light is too strong or the temperature is too high, side reactions may increase, resulting in a mixture of various brominated products, which is unfavorable for the separation and purification of 2% 2C4-dibromopentane. On the contrary, if the reaction conditions are too mild, the reaction rate will be slow and the yield will not reach the ideal. Therefore, during the preparation process, repeated experiments are required to find the best reaction conditions to obtain a higher yield and purity of 2% 2C4-dibromopentane product.
    What are the precautions for using 2,4-dibromothiophene?
    2% 2C4-dibromopentane is also a chemical reagent. When using it, be careful.
    First, this substance is toxic and irritating, and can hurt the skin, eyes, enter the body or harm health. Therefore, when operating, protective equipment is necessary, such as gloves, goggles, masks, etc., to avoid direct contact and inhalation.
    Second, 2% 2C4-dibromopentane is active, and there is a risk of explosion in case of heat, open flame or oxidant. Store it in a cool and ventilated place, away from fire and heat sources, and do not mix with oxidants.
    Third, the place where this substance is used should be well ventilated to expel its volatile gas and reduce its concentration in the air, so as to avoid the risk of deflagration and poisoning. If it is used in experiments, it should be operated in a fume hood to ensure safety.
    Fourth, after use, the remaining 2% 2C4-dibromopentane and its waste should not be discarded at will, and must be disposed of in accordance with relevant regulations. Or hand it over to a qualified treatment agency, or use a suitable method to decompose and transform it to make it harmless.
    Fifth, the operator must be familiar with its properties and methods of use, and be aware of relevant emergency measures in advance. If there is a leak, quickly cut off the fire source, ventilate it, and evacuate to a safe place. Small leaks can be covered and swept with sand, etc.; large leaks must be contained, recycled, and then properly disposed of. If someone touches or inhales it, quickly move it to a fresh air place, and in severe cases, rush to the hospital.