3322-93-8 Usage
Description
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE, also known as Tetrabromoethylcyclohexane (TBECH), is an additive brominated flame retardant. It is a chemical compound that contains bromine atoms, which provide flame-resistant properties. TBECH is commonly used in various applications to enhance the fire safety of materials.
Uses
Used in Flame Retardant Applications:
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE is used as an additive brominated flame retardant for enhancing the fire resistance of materials. The presence of bromine atoms in the compound helps to slow down the combustion process and reduce the risk of fire.
Used in Domestic Applications:
In the domestic industry, 1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE is used as a flame retardant in various household products, such as textiles, plastics, and electronics. This helps to improve the safety of these products and reduce the risk of fire accidents.
Used in Industrial Applications:
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE is also used in the industrial sector as a flame retardant in various materials, such as insulation, coatings, and adhesives. This helps to improve the fire safety of industrial equipment and facilities.
Used in Biodegradation Research:
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE has been used in research to investigate the biodegradation kinetics in aerobic and anaerobic soil. This research helps to understand the environmental impact of brominated flame retardants and develop strategies for their safe disposal and management.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Halogenated aliphatic compounds, such as 1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE, are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
Fire Hazard
Flash point data for 1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE are not available; however, 1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE is probably combustible.
Check Digit Verification of cas no
The CAS Registry Mumber 3322-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3322-93:
(6*3)+(5*3)+(4*2)+(3*2)+(2*9)+(1*3)=68
68 % 10 = 8
So 3322-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12Br4/c9-4-8(12)5-1-2-6(10)7(11)3-5/h5-8H,1-4H2
3322-93-8Relevant articles and documents
Reaction of Aromatic and Unsaturated Compounds with the Potassium Permanganate/HCI (HBr) Acetonitrile Reagent
Liu, Lilian Kao,Lin, Ching-Shan
, p. 61 - 66 (2007/10/03)
Addition of hydrochloric or hydrobromic acid to a solution of potassium permanganate in acetonitrile produced a homogeneous mixture, which is suitable for laboratory chlorination or bromination, respectively. Aromatic compounds more reactive than alkylbenzenes can be chlorinated or brominated without additional catalyst. Alkenes and alkynes give the corresponding vicinal dihaloalkanes and vinyl halides. All reactions complete within two hours under mild condition (25-60 °C) with excellent to moderate yields.
