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3,3',5,5'-TETRABROMOBIPHENYL

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3,3',5,5'-TETRABROMOBIPHENYL Basic information

Product Name:
3,3',5,5'-TETRABROMOBIPHENYL
Synonyms:
  • PBB NO 80
  • 3,3',5,5'-TETRABROMOBIPHENYL
  • 1,3-Dibromo-5-phenylbenzene
  • 3,3',5,5'-Tetrabromobiphenyl, 35μg /mL in Isooctane
  • pbb 80
  • 3,3',5,5'-Tetrabromo-1,1'-biphenyl
  • 3,5,3',5'-TetrabroMo-biphenyl
  • 1,1'-Biphenyl, 3,3',5,5'-tetrabromo-
CAS:
16400-50-3
MF:
C12H6Br4
MW:
469.79
Product Categories:
  • Aryl
  • Building Blocks
  • C9 to C12
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Liquid Crystals
  • Materials Science
  • Organic and Printed Electronics
  • Organic Building Blocks
Mol File:
16400-50-3.mol
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3,3',5,5'-TETRABROMOBIPHENYL Chemical Properties

Melting point:
185-190℃
Boiling point:
401.8±40.0 °C(Predicted)
Density 
2.140±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Dichloromethane (Slightly)
form 
Solid
color 
White to Off-White
InChIKey
FXJXZYWFJAXIJX-UHFFFAOYSA-N
EPA Substance Registry System
1,1'-Biphenyl, 3,3',5,5'-tetrabromo- (16400-50-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
WGK Germany 
3
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3,3',5,5'-TETRABROMOBIPHENYL Usage And Synthesis

Uses

PBB 80 is a related compound of PBB 37 (P215150), a brominated biphenyls that can be used as a flame retardant and often incorporated into consumer products including appliances, electronics and plastics.

Uses

3,3',5,5'-TETRABROMOBIPHENYL can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.

Preparation

1,3,5-tribromobenzene (6.3 g, 20 mmol) was dissolved in diethylether (50 ml). The reaction solution was cooled to -78° C., and n-butyllithium (8.8 ml, 22 mmol, 2.5M in hexane) was gradually added thereto. The reaction mixture was stirred at -78° C. for one hour, and copper chloride (II) (2.96 g, 22 mmol) was added thereto at -78° C. The reaction solution was stirred for five hours and washed with distilled water and ethylacetate at room temperature. The obtained ethylacetate layer was dried over MgSO4, and then dried under a reduced pressure to obtain a crude product. The crude product was purified by silica gel column chromatography to give intermediate A as a white solid (3.74 g, yield: 80%).

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