Production Method 1

87-82-1

Reaction Conditions

1.1 Reagents: Bromine ,  Chlorine Catalysts: Aluminum Solvents: Carbon tetrachloride

Reference

Method for manufacturing aromatic compounds

, Poland, , ,

Production Method 2

87-82-1

Reaction Conditions

1.1 Reagents: Iron ,  Bromine ,  Chlorine Solvents: 1,1,2,2-Tetrachloroethane

Reference

Bromine derivatives of noncondensed aromatic com pounds

, Belgium, , ,

Production Method 3

106-37-6

87-82-1

Reaction Conditions

1.1 Reagents: Iron ,  Sulfur trioxide ,  Iodine ,  Sulfuric acid ,  Bromine

Reference

Reaction of aryl Grignard reagents with hexahalobenzenes: novel arenes via multiple aryne sequence

Harada, Katsumasa; Hart, Harold; Frank Du, Chi Jen, Journal of Organic Chemistry, 1985, 50(26), 5524-8

Hexabromobenzene Raw materials

• 1,4-Dibromobenzene

Hexabromobenzene Preparation Products

• Hexabromobenzene (87-82-1)

• 1. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210
• 2. An antimonate pyrochlore (H1.23Sr0.45SbO3.48) for photocatalytic oxidation of benzene: effective oxygen usage and excellent activity?
  Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
• 3. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
  Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
• 4. An analyte-triggered artificial peroxidase system based on dimanganese complex for a versatile enzyme assay?
  Suji Lee,Min Su Han Chem. Commun., 2021,57, 9450-9453
• 5. An approach to C–N activation: coupling of arenesulfonyl hydrazides and arenesulfonyl chlorides with tert-amines via a metal-, oxidant- and halogen-free anodic oxidation??
  M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Bromobenzenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Halobenzenes Bromobenzenes
• Solvents and Organic Chemicals Organic Compounds Organic Halides

Hexabromobenzene (CAS No. 87-82-1): Properties, Applications, and Environmental Considerations

Hexabromobenzene (CAS No. 87-82-1) is a brominated aromatic compound with the molecular formula C6Br6. This highly brominated benzene derivative has attracted significant attention in both industrial applications and environmental studies due to its unique chemical properties. As a halogenated organic compound, it serves as an important intermediate in various chemical syntheses and has been studied extensively for its flame-retardant properties.

The physical properties of Hexabromobenzene include a white to pale yellow crystalline appearance with a molecular weight of 551.49 g/mol. It has a melting point of 320-325°C and demonstrates low solubility in water but good solubility in organic solvents like toluene and dichloromethane. These characteristics make it particularly useful in specialized industrial applications of Hexabromobenzene, especially where thermal stability is required.

One of the most searched topics regarding Hexabromobenzene CAS 87-82-1 relates to its environmental persistence. Recent studies have focused on its behavior as a potential persistent organic pollutant (POP), with particular attention to its bioaccumulation potential. Researchers are actively investigating degradation pathways of Hexabromobenzene to better understand its environmental fate, especially in light of increasing concerns about brominated flame retardants in ecosystems.

In terms of applications, Hexabromobenzene uses primarily revolve around its role as a flame retardant synergist and chemical intermediate. It has been employed in the production of certain polymers and electronic materials where flame resistance is crucial. However, the industry is increasingly exploring eco-friendly alternatives to Hexabromobenzene in response to growing environmental regulations and consumer demand for sustainable products.

The synthesis of Hexabromobenzene typically involves the bromination of benzene under controlled conditions. This process has been optimized over the years to improve yield and purity, with current methods focusing on reducing byproduct formation. Analytical techniques for Hexabromobenzene detection have also advanced significantly, with modern chromatography methods allowing for precise measurement even at trace levels.

From a safety perspective, proper handling of Hexabromobenzene requires standard laboratory precautions. While not classified as acutely toxic, its potential for bioaccumulation warrants careful management. Current research trends include developing remediation techniques for Hexabromobenzene in contaminated environments, with particular focus on advanced oxidation processes and microbial degradation.

The market for Hexabromobenzene and related compounds has seen fluctuations in recent years due to changing regulations. Manufacturers are increasingly required to provide detailed Hexabromobenzene safety data and environmental impact assessments. This has led to innovations in production processes that minimize waste and improve efficiency.

Looking forward, the scientific community continues to study Hexabromobenzene environmental effects through long-term monitoring programs. These studies are particularly important for understanding the compound's behavior in different ecosystems and potential impacts on wildlife. Simultaneously, material scientists are investigating new applications for Hexabromobenzene that leverage its unique properties while addressing environmental concerns.

For researchers and industry professionals seeking Hexabromobenzene technical information, current literature emphasizes the importance of understanding its structure-activity relationships. The symmetrical arrangement of bromine atoms on the benzene ring gives the molecule particular characteristics that influence both its industrial utility and environmental behavior.

In conclusion, Hexabromobenzene (87-82-1) represents an important compound at the intersection of industrial chemistry and environmental science. As regulations evolve and alternative technologies emerge, the future applications of this compound will likely focus on specialized uses where its unique properties provide essential functionality while minimizing ecological impact.

• 615-54-3(1,2,4-Tribromobenzene)
• 27476-23-9(Benzene, tetrabromo-)
• 636-28-2(1,2,4,5-Tetrabromobenzene)
• 56480-06-9(Naphthalene, hexabromo-(7CI,9CI))
• 22311-25-7(Benzene,1,2,3,4-tetrabromo-)
• 26249-12-7(Benzene, dibromo-)
• 108-36-1(1,3-Dibromobenzene)
• 626-39-1(1,3,5-Tribromobenzene)
• 28779-08-0(Benzene, tribromo-)
• 22245-33-6(Naphthalene,1,2,3,4,5,6,7,8-octabromo-)