1-Bromo-2-Chloro-4-Tert-Butylbenzene
Linshang Chemical
HS Code |
445992 |
Chemical Formula | C10H12BrCl |
Molecular Weight | 249.56 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 245 - 247 °C |
Density | Approx. 1.35 - 1.40 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | Around 105 - 110 °C |
Odor | Typical aromatic halogenated hydrocarbon odor |
Cas Number | Specific CAS number would need further literature search |
As an accredited 1-Bromo-2-Chloro-4-Tert-Butylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 100g of 1 - bromo - 2 - chloro - 4 - tert - butylbenzene packaged in a sealed glass bottle. |
Storage | 1 - Bromo - 2 - chloro - 4 - tert - butylbenzene should be stored in a cool, dry, well - ventilated area away from heat sources, open flames, and oxidizing agents. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials like glass or high - density polyethylene. Label the storage container clearly to prevent misidentification. |
Shipping | 1 - bromo - 2 - chloro - 4 - tert - butylbenzene is shipped in sealed, corrosion - resistant containers. It follows strict hazardous material regulations, with proper labeling and handling to ensure safe transportation due to its chemical nature. |
Competitive 1-Bromo-2-Chloro-4-Tert-Butylbenzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 1-Bromo-2-Chloro-4-Tert-Butylbenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
Cyanogen is highly active. It is connected by a carbon-nitrogen triple bond, which contains a lot of high energy, so that the cyanyl group exhibits unique behavior in many reactions. When encountering nucleophiles, it often acts as a nucleophilic substitution or addition, such as with alcohols, or to form nitrile ether derivatives. If it reacts with water under specific conditions, it can be hydrolyzed into carboxylic acids or amides. And cyanides are mostly toxic, because they can bind to cytochrome oxidase, disturb the respiratory chain of cells, and cause poisoning in organisms.
Xenon is a rare gas with stable chemical properties under normal conditions, and appears to be "independent". However, under certain extreme conditions, such as the presence of strong oxidizing agents and supplemented by high temperature and high pressure, xenon can also form bonds. It can form a variety of fluorides with fluorine, such as xenon difluoride, xenon tetrafluoride, etc. These fluorides are strong oxidants and can be used as fluorination reagents in the field of organic synthesis to introduce fluorine atoms to change the physical and chemical properties of compounds.
As for tert-butylbenzene, benzene rings are aromatic and relatively stable in nature, and can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. Tert-butyl is attached to the benzene ring, because it is the power supply group, which can increase the electron cloud density of the benzene ring, making the electrophilic substitution reaction more likely to occur, and the substitution positions are mostly in the adjacent and para-position. Tert-butyl itself also has characteristics, with large steric resistance, which has a significant impact on the reaction selectivity. In some reactions, specific structural products can be obtained by virtue of its spatial effect.
In summary, 1 + -cyanogen-2-xenon-4-tert-butylbenzene, the activity of cyanogen, the special reactivity of xenon and the properties of tert-butylbenzene are intertwined, and together they build a unique chemical property picture of this compound, which may open a new chapter of exploration in the fields
Arsenic is also toxic, but it is involved in medicine, agriculture and chemical industry. In ancient times, arsenic was used to treat malaria and syphilis. Today, small doses of arsenic can treat certain leukemia. In agriculture, arsenide has been used as an insecticide and herbicide, but it is gradually replaced because it pollutes soil and water sources. In chemical industry, arsenic is used to make alloys, semiconductor materials, etc.
Acetaminophen is a commonly used antipyretic and analgesic drug, which is mostly used to relieve fever caused by colds and influenza, and can also relieve mild to moderate pain, such as headache, joint pain, toothache, etc. Its mechanism of action is to inhibit the synthesis of prostaglandin, achieving antipyretic and analgesic effects. However, if used in excess, it can cause serious liver damage, so it should be used according to the doctor's advice, and the dose should not be increased.
First, the corresponding phenols are used as the starting materials. First, let the phenolic compound react with the tert-butylation reagent under suitable conditions to introduce the tert-butyl group. Commonly used tert-butylation reagents such as tert-butyl alcohol and tert-butyl chloride, etc. Under the catalysis of acidic catalysts such as concentrated sulfuric acid and p-toluenesulfonic acid, the phenolic ring of the phenol can undergo electrophilic substitution reaction and successfully connect to the tert-butyl group. Subsequently, through a specific oxidation reaction, the phenolic hydrox For example, a mild oxidizing agent, such as manganese dioxide, can be used to control the reaction temperature and time in a suitable solvent to achieve this conversion, resulting in the target product 1-hydroxy- 2-aldehyde-4-tert-butylbenzene.
Second, starting from benzaldehyde derivatives. Select benzaldehyde containing a suitable substituent, and introduce tert-butyl group through a similar electrophilic substitution reaction with tert-butylation reagent. After that, the hydroxylation operation is carried out for the ortho-position of the aldehyde group. In this step, a specific oxidation method can be used, such as the use of peroxides and other oxidants under alkaline conditions, to promote the hydroxylation of the aldehyde group ortho-site, and finally synthesize 1-hydroxyl-2-aldehyde-4-tert-butylbenzene.
Third, the organometallic reagent method is used. First prepare organometallic reagents containing tert-butyl groups, such as tert-butyllithium, tert-butylGrignard reagents, etc. Then react with suitable benzene ring derivatives, such as halogenated benzaldehyde or derivatives of benzaldehyde. During the reaction, the tert-butyl group in the organometallic reagent is connected to the benzene ring, and then through the subsequent appropriate conversion reaction, other substituents are adjusted to achieve the synthesis of 1-hydroxy-2-aldehyde-4-tert-butylbenzene. This method requires precise control of the reaction conditions to ensure the selectivity and yield of the reaction.
Mercury is a highly toxic substance that can evaporate at room temperature, and its vapor is also toxic. When storing, choose a cool, ventilated and dry place, away from fire and heat sources, to prevent mercury volatilization from increasing due to rising temperature. Packaging must be tight to prevent mercury leakage. During transportation, professional containers and vehicles must be used in accordance with the regulations on the transportation of hazardous chemicals to ensure transportation safety. Escort personnel should also be familiar with the hazards of mercury and emergency treatment methods.
Arsenic is also a toxic element. When storing, it should be stored separately from acids, alkalis and edible chemicals, and must not be mixed. The storage environment should be well ventilated to reduce the concentration of arsenic in the air. The packaging should be intact. If there is any damage, it must be dealt with in time. When transporting, it is also necessary to follow strict regulations and take protective measures to avoid arsenic leakage and pollution of the environment.
It is toxic and irritating to aminobenzene. Storage should be placed in a cool and ventilated warehouse, away from fire and heat sources. It should be stored separately from oxidants, acids, etc., and should not be mixed. Its packaging should be sealed to prevent moisture and deterioration. During transportation, it is necessary to ensure that the container does not leak, collapse, fall, or be damaged. It is strictly forbidden to mix with flammable or combustible materials, oxidants, etc.
In short, all three are dangerous. When storing and transporting, it is necessary to strictly follow relevant safety regulations and take protective and emergency measures to prevent endangering personal safety and the environment.
Cyanide is extremely strong in the environment. If it leaks out of the environment, it can cause water, soil and air pollution. If it flows into rivers, lakes and seas, aquatic organisms bear the brunt, and aquatic animals such as fish may die suddenly as a result, destroying the balance of water ecology. In the soil, it will change the chemical properties of the soil, affect the growth and development of plant roots, cause vegetation to wither, and damage the stability of the ecosystem. And cyanide evaporates in the air, forming a toxic gas mass, which is dissipated with the wind and deteriorates the surrounding atmospheric environment.
As for human health, cyanide is particularly harmful. It can enter the human body through the respiratory tract, skin and digestive tract. Once in the body, it quickly binds to cytochrome oxidase, blocking the respiratory chain of cells, causing cells to be unable to uptake and utilize oxygen, resulting in tissue hypoxia. When slightly poisoned, people will feel headache, dizziness, fatigue, and breathing difficulties; when the poisoning deepens, it can cause coma, convulsion, and even respiratory and heartbeat arrest, endangering life. Long-term exposure to cyanide-containing environments can also cause chronic poisoning, damage the nervous system, cardiovascular system, and immune system, making people vulnerable to various diseases, seriously compromising people's lifespan and quality of life.
Bromine, although slightly less toxic than cyanide, is also harmful. It is highly corrosive and irritating. In the environment, it can corrode metal facilities and accelerate the aging of building materials. For aquatic organisms, the accumulation of bromide can affect their reproduction and development, and change the population structure of organisms. In the human body, bromine can irritate the mucous membranes such as the eyes, nose, and throat, causing symptoms such as tears, coughing, and breathing difficulties. If it comes into contact with the skin, it will burn the skin, cause redness, swelling, and blisters.
4-tert-butylphenol is also not good. It is persistent in the environment and difficult to degrade. Residue in the soil will affect the activity of soil microorganisms and hinder the normal circulation of substances in the soil. In the aquatic environment, it will have toxic effects on aquatic organisms and reduce their chances of survival. On human health, 4-tert-butylphenol may interfere with the endocrine system, affect the normal secretion and regulation of hormones, long-term exposure or teratogenic, carcinogenic latent risk.
In short, cyanide, bromine, 4-tert-butylphenol and other substances pose a serious threat to the environment and human health, the world should be cautious to prevent its leakage and abuse, in order to protect ecological harmony and human well-being.

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