2,3-Dichloronitrobenzene
Linshang Chemical
HS Code |
497127 |
Chemical Formula | C6H3Cl2NO2 |
Molar Mass | 192.00 g/mol |
Appearance | Yellow to light brown solid |
Odor | Characteristic odor |
Melting Point | 43 - 45 °C |
Boiling Point | 255 - 257 °C |
Density | 1.547 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in benzene, toluene, etc. |
Vapor Pressure | Low vapor pressure |
As an accredited 2,3-Dichloronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 25 - kg drum packaging for 2,3 - dichloronitrobenzene chemical. |
Storage | 2,3 - dichloronitrobenzene should be stored in a cool, well - ventilated warehouse. Keep it away from sources of heat and ignition. Store it separately from oxidizing agents, reducing agents, and bases to prevent reactions. Ensure containers are tightly sealed to avoid leakage. Label storage areas clearly to prevent misuse. |
Shipping | 2,3 - dichloronitrobenzene is a hazardous chemical. It should be shipped in accordance with strict regulations. Use proper packaging to prevent leakage, and ensure carriers are trained to handle such substances during transportation. |
Competitive 2,3-Dichloronitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com


As a leading 2,3-Dichloronitrobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
In the field of ultraviolet absorbers, this compound has a significant effect. Because it can efficiently absorb ultraviolet rays, it is often added to plastics, coatings, rubber and other materials. After absorbing ultraviolet rays, it can effectively protect the material from aging and fading due to ultraviolet radiation, greatly prolonging the service life of the material. For example, in outdoor plastic products, adding an appropriate amount of 2% 2C3-dihydroxybenzophenone can make plastic products resist ultraviolet rays in sunlight for a long time, maintaining good physical properties and appearance.
In the cosmetics industry, 2% 2C3-dihydroxybenzophenone is also an important ingredient. It can be used as a sunscreen ingredient to help products resist the damage of ultraviolet rays to the skin. It absorbs ultraviolet rays, reduces the damage of ultraviolet rays to skin cells, and then protects the skin, reduces sunburn, tanning and photoaging problems, and provides necessary protection for the skin.
In the field of pharmaceutical synthesis, it is also an important intermediate. With its special chemical structure, it can participate in a variety of drug synthesis reactions. Many compounds with specific pharmacological activities require 2% 2C3-dihydroxybenzophenone as the starting material or key intermediate in the synthesis process, and through a series of chemical reactions, drug molecules with the effect of treating specific diseases are constructed.
In summary, 2% 2C3-dihydroxybenzophenone plays an indispensable role in the fields of ultraviolet absorbers, cosmetics and pharmaceutical synthesis, and has made great contributions to the development of related industries.
Looking at its appearance, under room temperature and pressure, it is mostly colorless to light yellow liquid, clear and transparent, like the quality of glaze, with a luster flowing and shining under the light. Its smell has a special aromatic smell. Although it is not strong and pungent, it is unique, and the smell is like being in a faint and rich environment.
When it comes to melting and boiling point, the melting point is relatively low, and it is often in a sub-zero state, making it difficult to condense into a solid state in ordinary low temperature environments. The boiling point is moderate, and when the temperature rises to a certain degree, it turns into curling steam and rises. This property allows it to exist stably in a liquid state within a specific temperature range, providing convenience for many chemical reactions and industrial applications.
Furthermore, its density is slightly lower than that of water. If mixed with water, it floats on the water, just like oil flowers floating in blue waves. And in terms of solubility, it has good solubility in common organic solvents, such as ethanol and ether, and can be fused with it. However, in water, the solubility is very small, and the two seem to be distinct and difficult to dissolve.
And its volatility is strong, and it is exposed to the air. In a short period of time, its amount can be seen gradually decreasing, turning into invisible steam and dispersing in the surrounding space. This volatility also allows it to quickly mix with air in a specific environment and play a corresponding role. And its refractive index also has a specific value. When light passes through, a specific refraction phenomenon occurs, which may have potential application value in the optical field.
In this compound, the introduction of fluorine atoms has a great impact on its chemical properties. Fluorine has extremely high electronegativity and can change the electron cloud distribution of molecules, which in turn affects its reactivity. Due to the presence of fluorine atoms, the polarity of 2% 2C3-difluorobenzylbenzene changes, and in some reactions, it may exhibit a different reaction path than fluorine-free analogs.
Its chemical stability is also enhanced by fluorine atoms. The fluorine-carbon bond energy is quite high, which makes it more difficult for the compound to break the chemical bond under some conditions. This property may be of important value in some application scenarios that require stability.
In the nucleophilic substitution reaction, the benzyl part of 2% 2C3-difluorobenzylbenzene may exhibit active reactivity. The benzyl carbocation is relatively stable due to the conjugation effect of the benzene ring, so it is vulnerable to attack by nucleophilic reagents. However, the electronegativity of the fluorine atom may affect the rate and selectivity of the nucleophilic substitution reaction.
In the redox reaction, the performance of this compound is also worthy of attention. Its molecular structure may affect its ability to gain and lose electrons, or participate in specific chemical reactions as oxidants or reducing agents.
In addition, the physical properties of 2% 2C3-difluorobenzylbenzene, such as melting point, boiling point, solubility, etc., are also related to its chemical properties, which together determine its application prospects in different fields.
One is a chemical synthesis method. This is a variety of chemical reactions, using carefully selected raw materials, through multiple steps to achieve the preparation of the target product. For example, selecting compounds with specific functional groups, under suitable reaction conditions, such as specific temperature, pressure and catalyst presence, prompts the breaking and recombination of bonds between molecules. Classical organic reactions such as condensation reactions and cyclization reactions are used to ingeniously construct the molecular structure of 2% 2C3-dihydrofuranylnaphthalene. This process requires fine control of reaction parameters to improve the purity and yield of the product. If the reaction conditions are slightly deviated, side reactions may multiply and affect the quality of the product.
The second is biosynthesis. This is the use of enzymes or microorganisms in living organisms to synthesize target compounds in a gentle way. Enzymes in living organisms are highly specific and can catalyze specific chemical reactions, and the reaction conditions are often close to room temperature and pressure, which is environmentally friendly. For example, microorganisms with specific metabolic pathways are screened and induced to synthesize 2% 2C3-dihydrofuranaphthalene by adjusting their culture conditions. Or the enzymes with corresponding catalytic activities are isolated and purified, and the reaction system is constructed in vitro for synthesis. However, biosynthesis also faces challenges, such as the complexity of microbial culture, the stability and activity maintenance of enzymes.
The third is the extraction of natural products. Some plants and microorganisms in nature may contain 2% 2C3-dihydrofuranylnaphthalene or its analogs. Appropriate extraction techniques, such as solvent extraction, supercritical fluid extraction, etc., can be used to obtain the target component from natural materials. Subsequently, high-purity 2% 2C3-dihydrofuranylnaphthalene can be obtained by separation and purification methods, such as column chromatography, high-performance liquid chromatography, etc. However, this approach is limited by natural resources, and the extraction process may be complicated and costly.
When storing, the temperature and humidity of the environment are the first priority. This material is delicate, and high temperature can easily cause qualitative changes, and high humidity may also lead to changes in its properties. Therefore, it is necessary to choose a cool and dry place to ensure its stability. In the warehouse, the temperature should be controlled in a specific range, and the humidity should also be constant in a moderate environment to prevent it from changing due to the disturbance of temperature and humidity.
Furthermore, avoiding light is also a priority. Light, or stimulate its chemical reaction, damage its essence. If it is to be stored in a place, it should be stored in a shading device, or placed in a dark corner to avoid light and protect it from light.
As for transportation, safety is the top priority. This object may be dangerous and must be properly packaged in accordance with relevant regulations. The packaging materials must be able to withstand pressure, shock, and leak. Loading and unloading should be done gently, so as not to collide, so as not to damage the package and cause it to be exposed. During transportation, pay close attention to changes in temperature and humidity. If there is any abnormality, dispose of it immediately to ensure its safety.
In addition, the transporter must be familiar with the nature of this object and know the emergency method. If there is a leak, we can quickly take appropriate measures to stop its spread and reduce its harm. During the whole process of storage and transportation, we should be cautious and follow the regulations to ensure the integrity of 2% 2C3-dihydrofuranylnaphthalene and avoid its harm.
Guanfu 2% 2C3-difluorobenzylbenzylbenzene, which is used in medicine, like a boat to help a boat, to create new paths for medicine. Doctors use it to enter the prescription, synthesize wonderful medicines, and cure various diseases. In the field of pesticides, it is like a divine weapon on the verge of war, which can make strong agents and protect crops, so that insects cannot be hidden, and diseases cannot be ravaged. As for material science, it is like a skilled craftsman who obtains good materials, develops new materials, endows materials with special abilities, and shines brightly in the genus of optoelectronics, which is used for future generations and opens up new horizons. It has a wide range of uses and has extraordinary achievements in various industries. It is sincerely a treasure in the chemical industry.
This substance is often colorless and transparent at room temperature, just like a clear spring in the mountains, clear and uncomplicated. Its appearance is like clear glaze, with a uniform texture and no turbidity at all. Looking at it, it gives people a sense of purity and clarity.
As far as its smell is concerned, it is quite slight and almost odorless. Smell it, there is no pungent taste, and there is no strong aroma. It is like an empty valley orchid, elegant and unassuming. This characteristic makes it easy to apply in an environment that requires strict odor without disturbing the surrounding breath.
Its density is slightly heavier than that of water. If it is placed in the same place as water, it can be seen that it sinks steadily, just like a humble gentleman, calm and heavy. This density characteristic can be used as an important reference in many process operations to help craftsmen accurately control the ratio and mixing of materials.
Furthermore, 2% 2C3-dihydroxypropyl ether has good solubility. It can easily blend in water and many common organic solvents, just like the water of a fish, without hindrance. This excellent solubility makes it able to quickly contact and react with other substances in chemical reactions, like a smart messenger, shuttling between molecules, causing all kinds of wonderful changes.
And its boiling point is moderate, neither too low to be easy to evaporate, nor too high to be difficult to control. At a suitable temperature, it can boil smoothly, just like a steady boat traveling in a river, providing stable conditions for the relevant production process, helping craftsmen to maximize their performance and create exquisite products.
This substance is hydrophilic. Because it contains dihydroxyl groups, hydroxyl groups, and hydrophilic groups, it can date with water and is soluble or partially soluble in water. This property is crucial in many application scenarios, such as the preparation of materials for aqueous systems, which can help them fuse with water and make the system more uniform and stable.
It is also reactive. Hydroxyl groups can participate in many chemical reactions, such as esterification reactions, which can be esterified with acid substances to form ester compounds. This reaction is used in the preparation of esters with special structures, which is of great significance for applications in perfumes, coatings and other fields. It can also participate in etherification reactions, interact with halogenated hydrocarbons and other substances to generate more complex ether structures, expanding its use in the field of organic synthesis.
Furthermore, the spatial structure and molecular properties of 2% 2C3 -dihydroxypropyl ether make it suitable for the preparation of surfactants. Its hydrophilic hydroxyl group and carbon chain part can form a specific amphiphilic structure, or help reduce the surface tension of liquids, and play a role in emulsification, dispersion and other processes, such as emulsion polymerization, cosmetic formulations, etc.
In addition, in biological related fields, because of its relatively mild structure and certain hydrophilicity, it can be used as a carrier of some bioactive substances to assist in the transportation and delivery of active ingredients, and may have potential application value in drug delivery systems. Its various chemical properties make it suitable for exploration and application in chemical, materials, biology and other fields.
To prepare 2% 2C3-dihydroxybenzaldehyde, catechol is often used as the starting material. Catechol, with active phenolic hydroxyl group, can be the basis of the reaction.
One method is to use catechol and chloroform as raw materials to react in an alkaline environment. Under the action of alkali, chloroform first forms the active intermediate of dichlorocarbenzene. This intermediate is extremely active and can rapidly undergo electrophilic substitution with the phenolic hydroxyl ortho-position of catechol. The alkali continues to act, neutralizing the reaction system, and then generating the precursor of 2% 2C3-dihydroxybenzaldehyde. After acidification to remove basic impurities, and then through extraction, distillation, recrystallization and other fine operations, pure 2% 2C3-dihydroxybenzaldehyde can be obtained.
The second method can utilize a variant of the Reimer-Tiemann reaction. Using catechol and trichloroacetaldehyde as starting materials, when the alkaline catalyst exists, trichloroacetaldehyde is induced by alkali, molecular rearrangement occurs, and an electrophilic intermediate is formed. This intermediate is combined with the hydroxy ortho-site of catechol, and after a series of complex reaction steps, acidification, purification and other processes, 2% 2C3-dihydroxybenzaldehyde can also be obtained.
There is also a method of using catechol and triethyl orthoformate as raw materials. Under the action of a specific catalyst, the ethoxy group of triethyl orthoformate is gradually replaced, and an intermediate product is formed first. The intermediate product is finally converted into 2% 2C3-dihydroxybenzaldehyde after hydrolysis, rearrangement and other reactions. Subsequent separation and purification are also required to obtain high-purity products.
All these production methods have advantages and disadvantages. It is necessary to carefully choose according to the actual required purity, yield and cost and many other factors to achieve the best preparation effect.
First, this product is toxic and may be harmful to health when it touches the human body. Therefore, when taking it, it is necessary to wear suitable protective equipment, such as gloves, goggles, etc., to prevent it from touching the skin, eyes and other parts. If you come into contact accidentally, you should immediately rinse with a lot of water, and according to the severity of the injury, seek medical treatment in a timely manner.
Second, 2% 2C3-dihydroxybenzene is easily oxidized in the air and has poor stability. When storing, it should be placed in a cool, dry and well-ventilated place, tightly sealed, to avoid excessive contact with air, and to keep away from fire and heat sources to prevent oxidative deterioration or fire.
Third, when conducting relevant experimental operations or industrial applications, it is necessary to precisely control its dosage and reaction conditions. Due to its active chemical properties, slight differences in reaction conditions may lead to very different reaction results. If participating in a chemical reaction, factors such as temperature and pH will have a significant impact on the reaction process and product formation, so it is necessary to strictly follow the operating procedures.
Fourth, 2% 2C3 - Dihydroxybenzene has special solubility and dissolves differently in different solvents. In actual use, the appropriate solvent should be selected according to the specific needs to achieve the desired effect. For example, some organic solvents may have good miscibility with them, but there may be risks such as flammability and explosion. When using, the pros and cons must be weighed and the choice should be made carefully.
Fifth, the waste 2% 2C3-dihydroxybenzene and related wastes should not be discarded at will. It is necessary to follow relevant environmental protection regulations and dispose of them properly to prevent pollution to the environment. Because of its certain toxicity, if not handled properly, it will cause harm to the ecological environment such as soil and water sources.

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