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3194-55-6

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3194-55-6 Usage

Halide flame retardants

Halide fire retardant is a kind of commonly-used organic fire retardants. The order of efficacy on fire retardancy for halogen element is I> Br> Cl> F. Because of that the C-F bond is very stable and is difficult to be broken down, so it has a poor fire-retardant effect. Moreover, owing to the poor thermal stability of the sulfonated, therefore, the industry usually applies chloride or bromide as the preferred fire retardant. The order of the fire-retardant effect of different kinds of organic compounds is that: aliphatic> cycloaliphatic> aromatic. However, the aliphatic compound has a poor thermal stability with the processing temperature should not exceed 205 ℃. In contrast, the thermal stability of the aromatic is relative good with the processing temperatures being up to 315 ℃. For the fire-retardant halide, they usually have relative high halogen content. Common halide fire retardants are as follows: Chlorinated paraffin is made from the direct chlorination of wax. It has a good chemical stability with low cost and a relative wide application. It is often used in combination with antimony trioxide. Full kelevan decane is generally produced by as following: first chloride the cyclopentadiene to yield hexachlorocyclopentadiene; then further go through dimerization under the catalysis of anhydrous aluminum chloride to obtain the final product. Hexabromocyclododecane belongs cycloaliphatic class fire-retardant and is mainly applied to the fire retardancy in polypropylene, polystyrene and polypropylene fibers. It is made as following: first put butadiene for trimerization, to first make cyclododecyl-1, 5, 9-triene, and then further have addition reaction with bromine in the carbon tetrachloride solution to obtain the 1, 2, 5, 6, 9, 10-Hexabromocyclododecane. Hexabromobenzene is produced from the bromination reaction of benzene with bromine in the tetrachloride solution with iron and sulfur as the catalyst. It is usually mixed with antimony trioxide. The current applied brominates fire-retardants include mainly tetrabromoethane, tetrabromo phenol disulfide, decabromodiphenyl ether, decabromodiphenyl, isocyanate-tris (2,6-dibromopropyl) ester, 2, 2-[4-(2,3-dibromopropyl-3,5-dibromophenyl] propane, hexabromocyclododecane decane, hexabromobenzene, tetrabromobisphenol A, octabromodiphenyl ethers, tetrabromodiphenyl ether, poly-dibromo-phenylene oxide, bis (tribromophenoxy) ethane, tribromophenol, ethylene bis tetrabromophthalimide dicarboxamide, pentabromobenzyl polyacrylate and so on. They respectively can be applied to plate of integrated circuit, unsaturated polyester, epoxy resin, polystyrene resin, chloroprene rubber, styrene-butadiene rubber, natural rubber, polyester resins, polypropylene, polyethylene wires, polyurethane, fiber, ABS resin, nylon, polybutylene terephthalate and so on. Put into the polystyrene (PS) (fire retardants), hexabromocyclododecane (fire retardants) and talc from the extruder into the feed section, and pump into the remaining foaming agent between the compression section and metering section to obtain a high compression-resistant foam sheet with a density of 34.7kg/m3 and water absorption of 0.09%.

Chemical Properties

It is white crystals and have two isomers with the melting point of low melting point type being 167-168 ℃ and high melting point type is 195-196 ℃. It has a good stability upon heat and ultraviolet light. The above information is edited by the lookchem of Dai Xiongfeng.

Uses

Different sources of media describe the Uses of 3194-55-6 differently. You can refer to the following data:
1. 1. It can be used in smoldering, for polystyrene foamed plastics, polypropylene and polyester, acrylic, polypropylene and other fabrics as smoldering finishing agent. 2. It is mainly used for thermoplastic and thermosetting polymers which have fire retardant requirements. It is particularly suitable for extrusion of foaming polystyrene. 3. It is used for the fire-retardant polystyrene of polypropylene plastics and fibers. It can also be used for the fire retardancy of finishing and leather double-sided coat after the fire-retardancy of polyester fabric. When used as additive fire retardants, it is especially suitable for polystyrene, unsaturated polyester, polycarbonate, polypropylene, synthetic rubber or the like.
2. 1,2,5,6,9,10-Hexabromocyclododecane(HBCD) was used to compare the efficiency of different advanced extraction techniques for the recovery of brominated flame retardants from styrenic polymers. It was used to study the kinetics of the thermal and photolytic segregation of HBCD using HPLC.

Production method

First synthesize trans, trans, cis-cyclododecene triene (see also 10850): add butyl titanate and diethyl aluminum chloride together into benzene; further add butadiene at a temperature below 55 ℃ and make trans, trans, cis-cyclododecene-1,5,9-triene (C12H18, [2765-79-9]) through Tri-polymerization reaction. Then further obtain hexabromocyclododecane through bromination. To a 2000 L enameled pot reactor equipped with a reflux cooler and exhaust processing apparatus 2000L, add 1300 L of ethanol and 278 kg of trans, cis-ring two two-1, 5, 9-triene and 872 kg of bromine with the feed temperature being 15-25 ℃. During the entire process of adding materials, upon maintaining the presence of free bromine ion, the reaction color was red. After the reaction, remove the excess amount of bromine needle and have generated hexabromocyclododecane be subject to filtration, refinement to obtain 1000 kg of products with the yield being 91%. Another approach is applying aluminum chloride as the catalyst. To 800 parts of the Cyclododecyl-1, 5, 9-triene and 1500 parts of ethanol, add 150 parts of aluminum trichloride at 15-25 ℃m, followed by the addition of 2400 parts of bromine at 25-30 ℃ within 2h; Stir and have the reaction for 5 hour at room temperature and then filter. The filtered cake was washed by 200 parts of ethanol and 2% sodium bicarbonate to obtain hexabromocyclododecane with the yield being 86%. Moreover, the supplement of halogenated hydrocarbons to the ethanol can further inhibit the formation of resinous substance.

General Description

1,2,5,6,9,10-Hexabromocyclododecane(HBCD) is a brominated flame retardant. It is used in the textile industry and polystyrene foam manufacturing. Electrochemical reduction of HBCD at carbon and silver cathodes has been studied using cyclic voltammetry and controlled-potential electrolysis.

Biochem/physiol Actions

1,2,5,6,9,10-Hexabromocyclododecane enhances the diet-induced body weight gain and metabolic dysfunction via disruption of lipid and glucose homeostasis in mice fed normal diet or high-fat diet.

Check Digit Verification of cas no

The CAS Registry Mumber 3194-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3194-55:
(6*3)+(5*1)+(4*9)+(3*4)+(2*5)+(1*5)=86
86 % 10 = 6
So 3194-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H18Br6/c13-7-1-2-8(14)10(16)5-6-12(18)11(17)4-3-9(7)15/h7-12H,1-6H2/t7-,8-,9-,10+,11+,12+

3194-55-6 Well-known Company Product Price

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  • Aldrich

  • (144762)  1,2,5,6,9,10-Hexabromocyclododecane  95%

  • 3194-55-6

  • 144762-25G

  • 271.44CNY

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3194-55-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5,6,9,10-Hexabromocyclododecane (HBCD)

1.2 Other means of identification

Product number -
Other names 1,2,5,6,9,10-hexabromo-cyclododecan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Flame retardants
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3194-55-6 SDS

3194-55-6Synthetic route

(1E,5E,9Z)-cyclododeca-1,5,9-triene
706-31-0

(1E,5E,9Z)-cyclododeca-1,5,9-triene

1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

Conditions
ConditionsYield
With sodium hypochlorite; hydrogen bromide; sodium sulfite In dichloromethane; cyclohexane; water at 0℃; for 0.0166667h; Flow reactor;97%
With pyridinium perbromide hydrobromide In methanol
cyclododeca-1,5,9-triene
4904-61-4

cyclododeca-1,5,9-triene

1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

Conditions
ConditionsYield
With bromine In dichloromethane; 2-methyl-propan-1-ol; chloroform at 14 - 15℃; pH=7; Large scale;96%
With bromine; sodium bromide In 2-methyl-propan-1-ol; chloroform; water at 10 - 15℃; for 4.5h; Solvent; Reagent/catalyst; Cooling with ice;94.9%
With hydrogen bromide; bromine In 2-ethoxy-ethanol at 50 - 90℃; for 17h; Temperature;92%
With 1-(-sulfonato)propyl-3-propanesulfonic acid imidazolium; hydrogen bromide; bromine In 2-ethoxy-ethanol at 50 - 90℃; for 8h; Temperature;90%
With bromine In 2-methyl-propan-1-ol; 1,2-dichloro-ethane at 30 - 50℃; for 5.25h;
(1E,5E,9E)-cyclododeca-1,5,9-triene
676-22-2

(1E,5E,9E)-cyclododeca-1,5,9-triene

1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

Conditions
ConditionsYield
With pyridinium perbromide hydrobromide In methanol
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

hydroxyhexabromocyclododecane

hydroxyhexabromocyclododecane

Conditions
ConditionsYield
With 5,10,15,20-tetraphenyl iron porphyrin In benzene at 25 - 30℃; for 24h; Temperature; Solvent; Reagent/catalyst; Inert atmosphere;40%
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

5,6-Dihydro-benzocycloocten
22368-66-7

5,6-Dihydro-benzocycloocten

Conditions
ConditionsYield
With potassium tert-butylate In diethylene glycol dimethyl ether
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

heptalene
257-24-9

heptalene

Conditions
ConditionsYield
Stage #1: 1,2,5,6,9,10-hexabromocyclododecane With 18-crown-6 ether; potassium tert-butylate In tetrahydrofuran at -100℃;
Stage #2: With potassium In tetrahydrofuran
Stage #3: With iodine In tetrahydrofuran
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

heptalene anion radical

heptalene anion radical

Conditions
ConditionsYield
Stage #1: 1,2,5,6,9,10-hexabromocyclododecane With 18-crown-6 ether; potassium tert-butylate In tetrahydrofuran at -100℃;
Stage #2: With potassium In tetrahydrofuran
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

di-trans-[12]annulene anion radical

di-trans-[12]annulene anion radical

Conditions
ConditionsYield
Stage #1: 1,2,5,6,9,10-hexabromocyclododecane With 18-crown-6 ether; potassium tert-butylate In tetrahydrofuran at -100℃;
Stage #2: With potassium In tetrahydrofuran cooling;
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

2,9-di-trans-[12]annulyne

2,9-di-trans-[12]annulyne

Conditions
ConditionsYield
Stage #1: 1,2,5,6,9,10-hexabromocyclododecane With potassium tert-butylate; dimethyl sulfoxide for 3h;
Stage #2: With bromine In tetrachloromethane for 2h; UV-irradiation;
Stage #3: With 18-crown-6 ether; potassium tert-butylate In tetrahydrofuran at -100.15℃; for 8h;
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

C12H10(2-)*2Cs(1+)

C12H10(2-)*2Cs(1+)

Conditions
ConditionsYield
Stage #1: 1,2,5,6,9,10-hexabromocyclododecane With 18-crown-6 ether; potassium tert-butylate In tetrahydrofuran at -100.15℃;
Stage #2: With o-chlorobenzylidene malononitrile In tetrahydrofuran at -100.15℃;
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

C12H12(1-)*K(1+)

C12H12(1-)*K(1+)

Conditions
ConditionsYield
With 18-crown-6 ether; potassium In tetrahydrofuran
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

trans-bicyclo<6.4.0>dodeca-2,4,6,9,11-pentaene
21657-72-7, 24844-26-6

trans-bicyclo<6.4.0>dodeca-2,4,6,9,11-pentaene

Conditions
ConditionsYield
With potassium tert-butylate In tetrahydrofuran at -80.15℃;
1,2,5,6,9,10-hexabromocyclododecane
3194-55-6

1,2,5,6,9,10-hexabromocyclododecane

A

(-)-(1R,2R,5R,6S,9R,10S)-1,2,5,6,9,10-hexabromocyclododecane

(-)-(1R,2R,5R,6S,9R,10S)-1,2,5,6,9,10-hexabromocyclododecane

B

(+)-(1S,2S,5S,6R,9S,10R)-1,2,5,6,9,10-hexabromocyclododecane

(+)-(1S,2S,5S,6R,9S,10R)-1,2,5,6,9,10-hexabromocyclododecane

Conditions
ConditionsYield
preparative chiral-phase liquid chromatography;

3194-55-6Relevant articles and documents

Salomon,Kochi

, p. 1889,1896 (1973)

Method for preparing hexabromocyclododecane

-

Paragraph 0023; 0024; 0025; 0026, (2018/09/08)

The invention discloses a method for preparing hexabromocyclododecane. A 1-methyl-3-propanesulfonic imidazole disulfate ion liquid catalyst is used. Compared with the hexabromocyclododecane prepared by a method in the prior art, the hexabromocyclododecane prepared by the method provided by the invention has the advantage that the melting point is improved and can reach 197 DEG C or higher. The method provided by the invention has the advantages that the cost is low; the operation is simple; safety and environment-friendly effects are achieved; the industrial application is easy.

A preparation method of double-ring (by machine translation)

-

Paragraph 0016; 0017, (2017/08/25)

The invention discloses a method for preparing-ring cyclododecane, including brominated, washing and separating, drying three steps. Bromide is the raw material ring dodecatrienoic and bromine are respectively drop adding isobutyl alcohol and dichloroethane in the mixed solvent, bromine and ring dodecatrienoic molar ratio of 3.05 - 3.08: 1. Dropping process is divided into three sections of heating up to 50 °C ± 2 °C, the total reaction time is 3 - 4 hours; washing and separating, in the bromination reaction compatibility of the separated solid phase into the dichloroethane with preparation of isobutyl alcohol mixed solvent, stirring and mixing and then separating the solid phase, then adding ethanol washing 2 times, filtered and the solid phase. The separation is washing the separated solid phase in 80 °C ± 2 °C drying, to obtain white solid powder product. The present invention provides a method for preparing cyclododecatriene, the method of washing of the solvent, the product is entrained will affect the melting point of the fully impurities not bromide, the product purity, make the product melting point rises. (by machine translation)

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