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1093632-34-8BrC1CC(Br)CC(Br)CC(Br)CC(Br)CC(Br)C1LEOCKULGXOQRTQ-UHFFFAOYSA-N1093632-34-8、25637-99-4DTXSID20891513Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
VerwendenThe commercially available brominated flame retardant hexabromocyclododecane (HBCD) is lipophilic, has a high affinity to particulate matter and low water solubility. It is used as a flame retardant additive, with the intent of delaying ignition and slowing subsequent fire growth during the service life of vehicles, buildings or articles, as well as while materials are stored. The main uses of HBCD are in flame-retarded expanded (EPS) and extruded (XPS) polystyrene foam insulation, with smaller scale use in textile applications and electric and electronic appliances (high impact polystyrene/HIPS). In textiles HBCD is used in back-coatings for upholstery and other interior textiles, including automotive applications.
synthetischeThe aliphatic flame retardant, hexabromocyclododecane (HBCD), is produced by the addition reaction of bromine to trans,trans,cis-1,5,9-cyclododecatriene, the cyclic trimer of butadiene. The HBCD that is obtained from this reaction consists of a mixture of stereoisomers of 1,2,5,6,9,10-hexabromocyclo-dodecane [3194-55-6] ranging from oils to an isomer with a 205–208℃ melting point. Commercially available HBCD contains a mixture of solid isomers and has a melting point range of 170–180 ℃ (185–195℃ ). Addition of bromine to the cyclic triene in nonpolar solvents results in substantial amounts of free-radical substitution reactions which lead to decreased yields and lower quality product. Use of polar solvents, such as ethanol, reduces the substitution reaction but can give rise to vicinal bromoethoxy by products. Mixed solvent systems, such as benzene–tert-butyl alcohol or perchloroethylene-ethanol,can be employed to improve product purities and yields. Another technique to reduce the formation of undesired byproducts is to add the bromine and cyclododecatriene simultaneously and sep- arately to ethanol. This process is carried out by separately feeding bromine and cyclo- dodecatriene in a molar ratio of 3 : 1 to 96 % ethanolinastirredreactor.The reaction temperature is kept at 20-30℃ and a 1-5% excess of bromine is maintained during the 2.5–3.0h addition. The precipitated product is recovered by filtration or centrifugation, and the mother liquor is recovered and reused in subsequent reactions after adding makeup ethanol. The total yield of dried HBCD from nine separate batches using recycled mother liquor is 92%.
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