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m-Terphenyl

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Identification
Molecular formula
C18H14
CAS number
92-06-8
IUPAC name
1,3-diphenylbenzene
State
State

At room temperature, m-terphenyl is in a solid state.

Melting point (Celsius)
86.00
Melting point (Kelvin)
359.15
Boiling point (Celsius)
389.00
Boiling point (Kelvin)
662.15
General information
Molecular weight
230.31g/mol
Molar mass
230.3130g/mol
Density
1.0338g/cm3
Appearence

m-Terphenyl is a white to light yellow crystalline solid.

Comment on solubility

Solubility of 1,3-Diphenylbenzene

1,3-Diphenylbenzene, often referred to in scientific circles by its systematic name, presents interesting characteristics when it comes to its solubility. Primarily, this compound is known for being:

  • Non-polar: Due to its hydrocarbon structure, 1,3-diphenylbenzene is largely hydrophobic.
  • Insoluble in Water: There is little to no solubility in polar solvents such as water, making it unfavorable for aqueous environments.
  • Soluble in Organic Solvents: It exhibits good solubility in organic solvents like benzene, toluene, and other non-polar solvents.

In general, the solubility of organic compounds like 1,3-diphenylbenzene can often be summarized by the phrase, "like dissolves like." This means that non-polar compounds tend to dissolve well in non-polar solvents, further emphasizing their limited solubility in polar environments.

When considering applications or reactions involving 1,3-diphenylbenzene, it's vital to acknowledge its solubility characteristics, as they greatly influence its behavior in various chemical processes.

Interesting facts

Exploring 1,3-Diphenylbenzene

1,3-Diphenylbenzene is an intriguing aromatic hydrocarbon that sparks interest in both synthetic and organic chemistry circles. Its molecular structure consists of a central benzene ring with two phenyl groups positioned at the 1 and 3 positions, showcasing its unique symmetry and stability.

Key Facts about 1,3-Diphenylbenzene

  • Structure and Symmetry: The compound's symmetry contributes to its *planarity*, allowing for effective π-π stacking interactions, which is essential in materials science.
  • Applications: It serves as a vital intermediate in the synthesis of other organic compounds, and its derivatives are utilized in various fields, including pharmaceuticals and industrial chemicals.
  • Thermal Properties: This compound exhibits interesting thermal stability, making it a candidate for research into high-performance materials.
  • Chemical Behavior: The presence of multiple phenyl groups significantly influences its reactivity, often making it resistant to certain types of chemical reactions.

As you delve into the world of 1,3-diphenylbenzene, consider the following quote from a notable chemist: "Understanding the subtleties of molecular interactions leads us to innovative applications that transform our technological landscape." This compound is a prime example of how *foundation chemistry* can pave the way for advancements in modern science.

In conclusion, the study of 1,3-diphenylbenzene not only enhances our understanding of aromatic compounds but also demonstrates the broader implications of molecular design in developing new materials and chemicals.

Synonyms
M-TERPHENYL
1,3-Diphenylbenzene
1,1':3',1''-Terphenyl
92-06-8
m-Diphenylbenzene
m-Triphenyl
1,3-Terphenyl
Isodiphenylbenzene
meta-terphenyl
1,1'-Biphenyl, 3-phenyl-
Diphenylbenzene
Terphenyls
3-Phenylbiphenyl
Gilotherm OM 2
NSC 6808
Benzene, m-diphenyl-
CCRIS 1656
WOI2PSS0KX
HSDB 2537
EINECS 202-122-1
DTXSID2029117
AI3-00860
NSC-6808
TERPHENYL, M-
EINECS 247-477-3
3-Phenyl-1,1'-biphenyl
AI3-01405
DTXCID209117
G 340
EC 247-477-3
T 3009
Terbenzene
CAS-92-06-8
UNII-WOI2PSS0KX
mTerphenyl
mTriphenyl
mDiphenylbenzene
1,3Terphenyl
1,3Diphenylbenzene
MFCD00003059
m-Terphenyl, 99%
1, 3-phenyl-
1,1'Biphenyl, 3phenyl
UNII-LFX1C55D2Z
LFX1C55D2Z
1,1':3',1''Terphenyl
1,1':3',1''-biphenyl
CHEMBL3184163
m-Terphenyl, analytical standard
NSC6808
Tox21_201579
Tox21_303528
AKOS002386404
CS-W010375
1,1':3',1''-Terphenyl (9CI)
NCGC00249075-01
NCGC00257320-01
NCGC00259128-01
AS-19308
DB-079227
NS00041387
T0018
F85603
AS-871/42732541
Q20965190
202-122-1
8042-11-3