4-Bromobiphenyl 99%...

4-Bromobiphenyl 99% for OLED Materials

4-Bromobiphenyl 99% for OLED Materials

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1 Gram

Negotiable

  • Min.Order :1 Gram
  • Purity: 99%min
  • Payment Terms : L/C,T/T,,MoneyGram,Other

Keywords

4-Bromobiphenyl 1,1’-Biphenyl,4-bromo- 4-Biphenyl bromide

Quick Details

  • Appearance:White Powder
  • Application:As OLED Intermediates and Pharmaceutical Intermediates
  • PackAge:1KG/Bag or Bottle,25KG per Box or Drum ,180KG,204KG Drum or Customized
  • ProductionCapacity:1|Metric Ton|Month
  • Storage:Keep sealed when not in use .
  • Transportation:By DHL /Fedex /TNT /EMS /Air /Sea etc.

Superiority:

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Details:

4-Bromobiphenyl Basic information
Product Name:    4-Bromobiphenyl
Synonyms:    (4-bromophenyl)benzene;1,1’-(biphenyl,-bromo-;1,1’-Biphenyl,4-bromo-;1,1’-biphenyl,-bromo-(4-bromobiphenyl);1’-Biphenyl,4-bromo-1;4-Biphenyl bromide;4-biphenylylbromide;4-Brom-biphenyl
CAS:    92-66-0
MF:    C12H9Br
MW:    233.1
EINECS:    202-176-6

 

4-Bromobiphenyl Chemical Properties
Melting point     82-86 °C(lit.)
Boiling point     310 °C(lit.)
density     0.9327
refractive index     1.6565 (estimate)
Fp     143 °C
solubility     dioxane: soluble1g/10 mL, clear, colorless to very faintly yellow
form     Crystalline Flakes
color     Almost white to slightly yellow
Water Solubility     Insoluble
BRN     1907453
Stability:    Stable. Incompatible with oxidizing agents.
InChIKey    PKJBWOWQJHHAHG-UHFFFAOYSA-N
CAS DataBase Reference    92-66-0(CAS DataBase Reference)
NIST Chemistry Reference    1,1'-Biphenyl, 4-bromo-(92-66-0)
EPA Substance Registry System    4-Bromobiphenyl (92-66-0)

 

4-Bromobiphenyl Usage And Synthesis
Chemical Properties    White powder
Uses    Intermediates of Liquid Crystals
General Description    Colorless crystals. Insoluble in water.
Air & Water Reactions    Insoluble in water.
Reactivity Profile    4-Bromobiphenyl may be sensitive to light. 4-Bromobiphenyl can react with oxidizing materials.
Fire Hazard    4-Bromobiphenyl is combustible.
Purification Methods    Crystallise the biphenyl from abolute EtOH and dry it in vacuo.[Beilstein 5 IV 1819.]

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