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4-Benzoylbiphenyl

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4-Benzoylbiphenyl Basic information

Product Name:
4-Benzoylbiphenyl
Synonyms:
  • LABOTEST-BB LT00159468
  • 4-PHENYLBENZOPHENONE
  • P-PHENYLBENZOPHENONE
  • (1,1’-biphenyl)-4-ylphenyl-methanon
  • [1,1’-biphenyl]-4-ylphenyl-methanon
  • 4-Biphenylyl phenyl ketone
  • 4-biphenylylphenylketone
  • 4-Diphenyl phenyl ketone
CAS:
2128-93-0
MF:
C19H14O
MW:
258.31
EINECS:
218-345-2
Product Categories:
  • FINE Chemical & INTERMEDIATES
  • Biphenyl derivatives
  • Photo Initiators
  • 2128-93-0
Mol File:
2128-93-0.mol
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4-Benzoylbiphenyl Chemical Properties

Melting point:
99-101 °C(lit.)
Boiling point:
419-420 °C(lit.)
Density 
1.0651 (rough estimate)
vapor pressure 
0Pa at 20℃
refractive index 
1.5500 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly, Heated)
form 
Solid
color 
White to Off-White
Water Solubility 
73.6μg/L at 20℃
BRN 
1876092
InChIKey
LYXOWKPVTCPORE-UHFFFAOYSA-N
LogP
4.7 at 35℃
CAS DataBase Reference
2128-93-0(CAS DataBase Reference)
NIST Chemistry Reference
Methanone, [1,1'-biphenyl]-4-ylphenyl-(2128-93-0)
EPA Substance Registry System
Methanone, [1,1'-biphenyl]-4-ylphenyl- (2128-93-0)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
24/25-36-26
WGK Germany 
3
RTECS 
PC4936800
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29143990

MSDS

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4-Benzoylbiphenyl Usage And Synthesis

Chemical Properties

SLIGHTLY YELLOW TO BEIGE CRYSTALLINE POWDER

Uses

4-Benzoylbiphenyl (4-Phenylbenzophenone; HRcure-PBZ ) is a reagent used to synthesize multicolored mechanochromic luminogen molecules. HRcure-PBZ is a low odor photoinitiator, which is a molecule that absorbs photons upon irradiation with light and forms reactive species out of the excited state, which initiates consecutive reactions.

Application

4-Benzoylbiphenyl (HRcure-PBZ) is a benzophenone analog with large aromatic ring systems. Sakamoto et al. investigated the properties of benzophenone ketyl radical analogs with large aromatic ring systems, such as naphthyl phenyl ketone, 4-benzoyl biphenyl, and bis(biphenyl-4-yl)methanone in the excited state by using nanosecond–picosecond two-color two-laser flash photolysis[1].

Flammability and Explosibility

Not classified

References

[1] Masanori Sakamoto. “Properties of Excited Ketyl Radicals of Benzophenone Analogues Affected by the Size and Electronic Character of the Aromatic Ring Systems.” Chemistry - A European Journal 12 6 (2006): 1610–1617.

4-Benzoylbiphenyl Preparation Products And Raw materials

Raw materials

Preparation Products

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