1 3 Dihydrobenzimidazole
quinoline thiophene imidazole thiazole

1,3-Dihydrobenzimidazole

    Specifications

    HS Code

    695187

    Name 1,3 - Dihydrobenzimidazole
    Molecular Formula C7H8N2
    Molar Mass 120.15 g/mol
    Appearance White to off - white solid
    Odor Odorless (usually)
    Melting Point 178 - 182 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Pka Around 11.5 (protonated form)
    Basicity Weakly basic
    Crystal Structure Typically forms orthorhombic crystals
    Stability Stable under normal conditions, but can react with strong oxidizing agents

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    Frequently Asked Questions

    As a leading 1,3-Dihydrobenzimidazole 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 1,3-dihydrobenzimidazole?
    Dioxanthracothiazole is a class of organic compounds with special structures, and its main uses are quite extensive. In the field of materials science, dioxanthracothiazole and its derivatives exhibit excellent photoelectric properties and are often used in the preparation of organic Light Emitting Diodes (OLEDs). This compound can efficiently convert electrical energy into light energy. The prepared OLEDs have the advantages of high luminous efficiency, wide viewing angle, and fast response speed. They are widely used in the manufacture of display screens, such as mobile phones, televisions, and computer displays, which greatly improve the display image quality and visual experience.
    In the field of chemical synthesis, dioxanthracothiazole can be used as a key synthesis intermediate. With its unique molecular structure and reactivity, chemists can modify and derive it through various chemical reactions, and then synthesize organic compounds with more complex structures and more specific functions. These derived compounds may have biological activities such as antibacterial and anti-cancer, providing novel lead compounds for drug development and helping to discover new therapeutic drugs.
    In addition, in the field of organic semiconductors, dioxanthracothiazole can be applied to the manufacture of organic field effect transistors (OFETs) because of its suitable energy band structure and carrier mobility. OFETs have broad application prospects in wearable electronic devices, flexible electronic devices and other fields, which can realize the flexibility and wearability of electronic devices, and open up new paths for the development of future electronic technologies.
    In summary, dioxyanthracenothiazole plays an important role in many fields such as materials science, chemical synthesis, and organic semiconductors, promoting the continuous progress and innovation of related technologies.
    What are the physical properties of 1,3-dihydrobenzimidazole?
    The physical properties of silicon dioxide and beryllium hafnium are as follows:
    silicon dioxide and beryllium hafnium, its texture is firm and brittle. It is often colorless and transparent, but it may also contain impurities and have a little color. Its crystal structure is delicate and has a high symmetry. The melting point of this substance is very high, and it needs to be extremely high temperature to melt it. It is like calcination with a hot fire, and it is difficult to easily make it invisible. Its boiling point is also quite considerable, and unusual temperatures can cause it to vaporize into steam.
    In terms of hardness, silicon dioxide and beryllium hafnium are quite hard, and ordinary objects are difficult to scratch their surface. It is like wearing a hard armor, and it is not afraid of slight scratching. Its density is moderate, among all kinds of substances, the proportion of space mass is just right, not too heavy, nor is it light.
    Furthermore, the chemical stability of silicon dioxide and beryllium and hafnium is quite good, and it is not easy to have violent chemical reactions with it in common acid and alkali environments. It is like a gentleman who does not change, and is not easily disturbed by the outside world. However, under specific extreme conditions, it will also show unique chemical activity, interacting with some special reagents, resulting in wonderful changes.
    And its optical properties are also unique, with a high transmittance of light. In the field of optics, it can often be used as raw materials for lenses, prisms and other devices, so that light can propagate according to the preset trajectory, contributing to the delicate operation of optical instruments.
    What are the chemical properties of 1,3-dihydrobenzimidazole?
    Dioxanthanothiophene, which is an important member of the field of organic semiconductor materials, has unique chemical properties.
    Bearing the brunt, it has excellent electron transport properties. The molecular structure of dioxanthanothiophene is cleverly designed, the conjugate system is extended, and the electron delocalization is good. Just like electrons travel freely on molecular orbitals, so the electron transport efficiency is quite good. This property is of great significance in electronic devices such as organic field effect transistors, which can greatly improve the device's carrier mobility, accelerate the electron migration rate, and then improve the device's working efficiency.
    Furthermore, it has good light absorption characteristics. In the visible region, dioxanthanothiophene can effectively absorb photons and generate electron-hole pairs. This is because the intramolecular electron transition energy level matches the visible light energy. Just like the tenon and mortise of precise docking, in the application of organic photovoltaic cells, it can efficiently capture light energy and convert it into electrical energy to improve the photoelectric conversion efficiency of photovoltaic devices.
    Stability is also its outstanding chemical properties. The chemical structure of dioxyanthracene-thiophene is stable, and it is difficult to react with other substances under common environmental conditions. This stability acts as a strong barrier to ensure that the material has lasting and stable neutral performance in various application scenarios, and is not easily disturbed by external factors such as temperature, humidity, light, etc., laying a solid foundation for its practical application.
    In addition, its solubility is also unique. Soluble in specific organic solvents, this property is significant in material processing and preparation. With the help of solution processing methods, such as spin coating, inkjet printing and other technologies, the material can be easily made into the required film or device structure, greatly expanding the flexibility of its preparation process and application range.
    What are the synthesis methods of 1,3-dihydrobenzimidazole?
    The synthesis method of dimethylfuranopyrazole has many ingenious methods from ancient times to modern times. For example, it can be divided into two ends.
    One is to reduce the reverse group.
    Take the alkylenopyrazole-containing nitrogen before, under the action of catalysis, the reverse reaction of the molecule is introduced. If the alkylpyrazole derivative raw material is used in the presence of gold catalysis, such as gold, etc., it can be added to the nucleus of its original molecules. In this way, gold catalyzes the activation of the alkylene part, making it easier for the nitrogen atom on the pyrazole to generate a reaction, and the rearrangement of the nitrogen atom in the first system is the most important.
    Second, the rearrangement strategy of dimethylfuranopyrazole is used. First synthesize the product with specific properties, and then promote its regeneration and rearrangement under appropriate conditions. For example, synthesize pyrazole derivatives containing enol ether groups. Under the action of acid or chemical catalysis, the enol ether is partially regenerated, and the enol-ketone interaction is reduced. It is accompanied by the nucleus reaction of the molecule to form the skeleton of difuran-pyrazole. In this process, factors such as the amount of catalysis, the degree of reaction, and the degree of reaction are very important, and precise control is required to obtain the ideal product.
    Third, the use of multiple partitions is reversed. Many different partitions, such as aldose, ketone, and nitrogen-containing compounds, are reversed in the same reaction system. Each component interacts, sequentially generating a series of inverse molecules, such as synthesis and transformation, one step. The advantage of this method is that it can greatly synthesize the pathway, improve the synthesis efficiency, and introduce multiple substituents through the modification of the molecular weight, thus enriching the polymorphism of difuran-pyrazole derivatives. However, it is necessary to perform the inverse reaction of the inverse parts in order to ensure the matching of the inverse reaction rate of each inverse reaction.
    In which fields is 1,3-dihydrobenzimidazole used?
    1% 2C3 + - + dicyanoanthracothiazole is used in many fields. In the field of optoelectronic devices, it plays a key role in the manufacture of organic Light Emitting Diode (OLED) with its unique optoelectronic properties. OLED has the advantages of high contrast, wide viewing angle, and fast response due to its self-luminous properties. 1% 2C3 + - + dicyanoanthracothiazole can optimize the performance of the luminous layer, improve the luminous efficiency and stability, and make the display picture clearer, brighter, and more realistic. It is widely used in display devices such as mobile phones and televisions.
    In the field of organic solar cells, 1% 2C3 + - + dicyanoanthracothiazole can act as an electron receptor material. Organic solar cells have attracted much attention due to their lightweight and flexible manufacturing advantages. This material can enhance the absorption of light and charge transfer efficiency of the battery, improve the photoelectric conversion efficiency of the battery, and promote the utilization of solar energy to a more efficient and convenient direction. Contributing to the development of renewable energy.
    In the field of chemical sensors, 1% 2C3 + - + dicyanoanthracothiazole has sensitive response characteristics to specific substances. With the help of optical or electrical properties changes caused by its interaction with the target analyte, highly selective detection of ions, molecules and other substances can be achieved. For example, in environmental monitoring, it can accurately detect heavy metal ions in water; in the biomedical field, it can detect specific biomarkers in organisms, providing an effective means for environmental and biomedical detection.
    In conclusion, 1% 2C3 + - + dicyanoanthranothiazole has shown important application value in the fields of optoelectronic devices, organic solar cells, and chemical sensors due to its unique structure and properties, and continues to promote technological innovation and progress in various fields.