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3,4,5,6-Tetramethylphenanthrene

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Identification
Molecular formula
C18H18
CAS number
826-73-3
IUPAC name
3,4,5,6-tetramethylphenanthrene
State
State
At room temperature, 3,4,5,6-tetramethylphenanthrene is in a solid state, characterized by aromatic hydrocarbon features due to its polycyclic structure.
Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
232.36g/mol
Molar mass
232.3550g/mol
Density
1.0385g/cm3
Appearence

3,4,5,6-Tetramethylphenanthrene appears as a crystalline solid. It is notable for its distinct polycyclic aromatic hydrocarbon structure, made evident by its aromatic ring system and methyl group substitutions.

Comment on solubility

Solubility of 3,4,5,6-tetramethylphenanthrene

3,4,5,6-tetramethylphenanthrene is an organic compound known for its complex aromatic structure, which significantly influences its solubility characteristics. This compound is primarily characterized by:

  • Low Solubility in Water: Due to its large and hydrophobic nature, 3,4,5,6-tetramethylphenanthrene shows very limited solubility in water. The presence of multiple methyl groups increases hydrophobic interactions, making it less likely to interact with polar solvents.
  • Solubility in Organic Solvents: In contrast, this compound is readily soluble in a variety of organic solvents such as:
    • Benzene
    • Toluene
    • Xylene
  • Temperature Dependency: As with many organic compounds, the solubility can increase with temperature, highlighting the importance of temperature control in experimental settings.

To conclude, the solubility profile of 3,4,5,6-tetramethylphenanthrene is a reflection of its molecular structure, offering insights into its potential applications and behavior in various chemical environments. As noted, its hydrophobic nature makes it a candidate for use in situations where water solubility would be a disadvantage.

Interesting facts

Exploring 3,4,5,6-Tetramethylphenanthrene

3,4,5,6-tetramethylphenanthrene is a fascinating polycyclic aromatic hydrocarbon (PAH) that attracts interest due to its complex structure and unique properties. Here are several intriguing aspects of this compound:

  • Natural Occurrence: This compound can be found in various types of coal tar and crude oil, showcasing its relevance in natural processes.
  • Synthesized in the Laboratory: Researchers often synthesize 3,4,5,6-tetramethylphenanthrene to study its characteristics and reactions, contributing to a better understanding of PAHs.
  • Environmental Concerns: Like many PAHs, this compound is considered a pollutant due to its potential carcinogenicity. Studying its behavior in the environment is crucial for assessing the impact of industrial activities.
  • Applications in Science: Beyond its natural occurrence, 3,4,5,6-tetramethylphenanthrene is also utilized in scientific research and experimentation, particularly in studying chemical reactions involving aromatic compounds.
  • Cultural Significance: PAHs, including 3,4,5,6-tetramethylphenanthrene, often appear in studies related to the history of fossil fuels and the origins of carbon-based life forms, bridging chemistry and our understanding of Earth’s history.

The study of 3,4,5,6-tetramethylphenanthrene offers a window into the world of organic chemistry, revealing how complex structures influence chemical behavior and environmental impact. Chemists and students alike explore this compound to better understand the broader implications of PAHs in our world.

Synonyms
3,4,5,6-TETRAMETHYLPHENANTHRENE
Phenanthrene, 3,4,5,6-tetramethyl-
7343-06-8
DTXSID80223659
DTXCID60146150
buslhlosctvnrq-uhfffaoysa-n
NS00095886