2 Acetyl 3 Hydroxythiophene
quinoline thiophene imidazole thiazole

2-Acetyl-3-Hydroxythiophene

Taiy Chemical

    Specifications

    HS Code

    735400

    Chemical Formula C6H6O2S
    Molar Mass 142.18 g/mol
    Appearance Yellow - to - light brown liquid
    Boiling Point 242 - 244 °C
    Melting Point 40 - 42 °C
    Density 1.294 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, diethyl ether
    Flash Point 106 °C
    Odor Characteristic sulfur - containing odor

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    General Information
    Where to Buy 2-Acetyl-3-Hydroxythiophene in China?
    As a trusted 2-Acetyl-3-Hydroxythiophene 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-Acetyl-3-Hydroxythiophene 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-acetyl-3-hydroxythiophene?
    2-% ethyl-3-furanyl ketone is also an organic compound. Its main use is quite extensive, and it has a significant effect in the field of fragrances. Because of its unique aroma, it is often used as a fragrance component to add special flavor and aroma to the preparation of various flavors, such as food flavors and daily chemical flavors. In the food industry, it can give food a wonderful aroma, improve quality and attractiveness. In daily chemical products, such as perfumes, air fresheners, etc., it can increase fragrance and create a pleasant atmosphere.
    In the field of medicine and chemical industry, 2-% ethyl-3-furanyl ketone also has important uses. It is often used as an intermediate in organic synthesis and is used to prepare a variety of drugs and biologically active compounds. With its specific chemical structure, through a series of chemical reactions, molecular structures with specific pharmacological activities can be constructed, providing key basic raw materials for pharmaceutical research and development and production.
    In the field of organic synthetic chemistry, this compound is a key intermediate and participates in the construction of many complex organic molecules. Chemists use its special structure and reactive activity to design and implement various organic synthesis routes to synthesize organic compounds with specific functions and structures, and promote the development of organic synthetic chemistry.
    Although "Tiangongkai" does not describe 2-% ethyl-3-furanyl ketone in detail, from an ancient perspective, the use of such compounds in later generations is a manifestation of ingenuity. From the delicate preparation of fragrances, to the practicality of pharmaceutical chemicals, to the innovation of organic synthesis, all demonstrate human's in-depth understanding and ingenious use of material properties, which is the crystallization of technology and wisdom.
    What are the physical properties of 2-acetyl-3-hydroxythiophene?
    2-%E4%B9%99%E9%85%B0%E5%9F%BA-3-%E7%BE%9F%E5%9F%BA%E5%99%BB%E5%90%A9, this is a special material with extraordinary physical properties.
    Its quality is strong and tough, like the solidification of gold and stone, it can withstand great force without folding, and it will not bend under heavy pressure. Its hardness is comparable to that of stainless steel, but it does not lose its agility, and it is not as brittle and fragile as ordinary hard objects. When external force is added, it can be moderately deformed to unload its force, and then return to its original state, just like the flexibility of a snake.
    Furthermore, its heat conduction is very different. Heat travels on it, like water rushing, passing quickly, and it can make the temperature uniform in an instant. Touching it in winter, the cold is difficult to invade, like holding warm jade; stroking it in summer, the heat suddenly disappears, like Linqing Spring. This feature makes it useful for thermostats and things that keep heat and cold.
    It also has its electrical conductivity, which is like lightning sweeping the air, fast and unimpeded. If the current passes through it, the loss is almost no, which can make the travel of electrical appliances more efficient and reduce energy consumption sharply. In order to make wires, electricity can be transmitted far away without losing its power, like the water of a river flowing for thousands of miles without exhaustion.
    In addition, its light reflection and refraction are also wonderful. Light shines on it, or like the reflection of a mirror, a clear reflection, which is unpleasant; or like the refraction of glaze, it emits colorful light, which is beautiful. Using this as a mirror, you can see the subtleties of all things; using optical instruments, you can see the secrets of heaven and earth.
    As for its density, it is between the light and heavy, neither as light as a feather and difficult to hold, nor as heavy as a boulder. This moderate state makes it suitable for many utensils, or hanging in the air, or placed on the ground, all of which can be stable and not falling, and still.
    The physical properties of 2-%E4%B9%99%E9%85%B0%E5%9F%BA-3-%E7%BE%9F%E5%9F%BA%E5%99%BB%E5%90%A9 are unique and very unique, and they hide endless potential in various fields, which is a rare treasure in the world.
    Is the chemical properties of 2-acetyl-3-hydroxythiophene stable?
    2-% ethyl-3-furanyl ketone, this is an organic compound, and its chemical properties are quite stable under certain conditions.
    Look at its structure, containing carbonyl and furan rings. Carbonyl is the activity check point, but in the usual environment, its reactivity may be restricted due to the action of surrounding groups. Furan rings are aromatic, giving the compound a certain stability.
    Under normal temperature and pressure, if there is no specific reagent or excitation conditions, 2-% ethyl-3-furanyl ketone can generally maintain a relatively stable state. When encountering specific chemicals such as strong acids, strong bases or strong oxidants, its stability will be challenged.
    In case of strong acid, carbonyl oxygen atoms may protonate, causing changes in the distribution of molecular electron clouds, enhancing reactivity, or triggering reactions such as nucleophilic addition. When encountering strong bases, its α-hydrogen atoms may be taken away, and subsequent reactions occur.
    In an oxidizing environment, strong oxidants may attack the furan ring or carbonyl group, causing structural changes. However, under common mild conditions, such as room temperature, ordinary atmospheric environment, and no special chemical action, 2-% ethyl-3-furanyl ketone can maintain stability, and its chemical properties are relatively inactive. It can maintain its own structure and properties for a long time.
    What are the preparation methods of 2-acetyl-3-hydroxythiophene?
    To make di-ethyl-3-furanyl ketone, there are various methods. The ancient good work is often done by the ancient method. Although the years have passed, the method has many subtleties, which can also be used as a lesson today.
    First, the method of acylation is carried out with furan and appropriate acylating reagents. If an acyl halide is used as an acylating agent, under suitable catalysts and reaction conditions, the two are combined. Furan is aromatic, and the electron cloud distribution on its ring is specific. The acyl halide generates an electrophilic reagent under the action of the catalyst, attacks the specific position of the furan ring, and then forms the precursor of di-ethyl-3-furanyl ketone. After appropriate modification steps, the target product can be obtained. In this process, the choice of catalyst, the control of reaction temperature and time are all key.
    Second, the compound containing di-ethyl-3-furan is used as the starting material and is converted into a functional group. For example, the furan derivative with suitable substituents is gradually converted into a methanone group through a series of reactions such as oxidation, reduction, and condensation. When oxidizing, a mild oxidizing agent should be selected to prevent damage to the furan ring; when condensing, the reaction should be directed to occur and the desired structure can be obtained.
    Third, the strategy of constructing the furan ring can be achieved. First, a suitable chain compound is used to form the furan ring through cyclization reaction, and di- ethyl and methyl ketone groups are introduced. This requires careful design of the structure of the chain-like raw materials, so that the activity of each reaction check point is appropriate, the cyclization reaction is carried out smoothly, and the position and configuration of the substituent can be precisely controlled.
    All these methods have advantages and disadvantages. Although the method of acylation is direct, the reaction conditions may be severe; the process of functional group transformation may be complicated; the strategy of constructing furan ring may not be easy to prepare raw materials. However, those who are good at work can choose the best method according to local conditions in time to obtain a pure product. Those who make this product need to understand the principles of chemistry, be familiar with the skills of operation, and evaluate the situation in order to achieve its work.
    What is the price of 2-acetyl-3-hydroxythiophene in the market?
    The price of di-ethyl-3-furanyl ketone in today's market is determined by many reasons.
    Its price is first related to the price of raw materials. The manufacture of di-ethyl-3-furanyl ketone requires specific raw materials. If the production of raw materials changes due to time, land conditions, and political regulations, its price will also change. If the raw materials are rare, they need to be purchased at a high price, which will increase the cost of di-ethyl-3-furanyl ketone and increase its price in the market.
    The coarseness of the manufacturing process is also a major reason. Sophisticated craftsmanship can increase productivity, reduce energy consumption, and reduce production costs. If the craftsmanship is advanced, the manufacturer can lower the price to compete for the market, and the price may be lower; on the contrary, the craftsmanship is poor, the cost is high, and the price is also high.
    The supply and demand of the city, especially the price. If the market is prosperous, the demand exceeds the supply, and the manufacturer may raise the price to obtain a big profit; if the supply exceeds the demand, the manufacturer will sell the goods, or reduce the price to promote sales. In addition, competition in the same industry also has an impact. There are many manufacturers in the market, competing for customers, or reducing the amount of profit and demand, causing the price to fall; if the manufacturer is few, it will be monopolized, and the price may be controlled by it and
    Furthermore, the regulation of government and the amount of tax also affect the price of di-ethyl-3-furanyl ketone. The government regulations are harsh, and the cost of the manufacturer's compliance with the regulations increases, and the price may rise; the heavy tax also makes the cost rise and the price high.
    In summary, the market price of di-ethyl-3-furanyl ketone is difficult to determine due to the combination of raw materials, craftsmanship, supply and demand, competition, government taxes and other factors. To know the real-time price, it is necessary to carefully observe the market conditions and study the changes in various factors.