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Terphenyl
is an aromatic hydrocarbon consisting of three
benzene rings connected to each other in either ortho, meta or para positions
without any additional functionalization. This structure does not allow the fusion of benzene ring.
Terphenyl structure is therefore not very reactive.
Though pure terphenyl is a white crystalline solid,
commercial grades are light yellow waxy-like flakes
at room temperature, with a faint, pleasant odour. It
is insoluble in water. Commercial mixture grade consists
of generally o-terphenyl 2-10%, m- 45-49%, p-
25-35% and higher polyphenyls 2 to 18% with trace amounts
of bidiphenyl.
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Product
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o-Terphenyl
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m-Terphenyl
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p-Terphenyl
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CAS
RN
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84-15-1
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92-06-8
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92-94-4
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Melting
point
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56.2
C
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87.5
C
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212.7
C
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Boiling
point
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332
C
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365
C
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376
C
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Terphenyl is used as a
preservative to prevent the growth of molds and fungus in combination with other
antioxidants. Terphenyl is a starting material for the production of polychlorinated terphenyls,
which are once used industrially as heat storage and transfer agents. Terphenyl is also used as an intermediate for the production of target
organic compounds such as non-spreading lubricants, emulsifiers, optical brighteners, crop protection
products, and plastics. m-Terphenyl is used in thermal printing material and
as a coolant in nuclear reactors, and p-terphenyl as
a laser dye and a sunscreen lotion component. It is
used as a particle of radiation detector
which operates through emission of light flashes (the emission maximum at 343 nm, lower maxima at 325 and 327 nm)
that are detected by a
photosensitive device. Some terphenyl derivatives are under study for useful as a pharmaceutical
ingredient such as immunosuppressive, antiinflammatory and
antitumor agents. Fluorine-substituted terphenyls are used as a component of liquid crystalline for
high voltage holding ratio, low threshold voltage, and
broad temperature
range layers applications.
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