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2-Ethylphenanthrene

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Identification
Molecular formula
C16H14
CAS number
2810-39-9
IUPAC name
2-ethylphenanthrene
State
State

At room temperature, 2-Ethylphenanthrene is a solid.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
331.30
Boiling point (Kelvin)
604.45
General information
Molecular weight
206.31g/mol
Molar mass
206.3060g/mol
Density
1.0697g/cm3
Appearence

2-Ethylphenanthrene appears as a pale yellow crystalline solid.

Comment on solubility

Solubility of 2-ethylphenanthrene

2-ethylphenanthrene, a polycyclic aromatic hydrocarbon, exhibits specific solubility characteristics due to its molecular structure. Understanding its solubility is crucial for various applications, including environmental science, organic chemistry, and materials science. Here's a breakdown of its solubility properties:

  • Solvent Compatibility: 2-ethylphenanthrene is more soluble in non-polar solvents such as benzene, toluene, and other hydrocarbons due to its hydrophobic nature.
  • Water Solubility: This compound is characterized by its very low solubility in water, often regarded as practically insoluble. This means that in aqueous environments, it tends to resist dissolution.
  • Temperature Effects: The solubility of 2-ethylphenanthrene can slightly increase with higher temperatures, as is common with many organic compounds, but it remains predominantly non-polar and hydrophobic.
  • Environmental Impact: Due to its low water solubility, 2-ethylphenanthrene can accumulate in sediment and soil, posing potential risks to aquatic life.

In summary, the solubility characteristics of 2-ethylphenanthrene are largely defined by its hydrophobic properties, making it suitable for use in organic solvent systems while limiting its interaction with water environments. This highlights the importance of managing its presence in ecosystems, especially in localized areas where it may persist in the environment.

Interesting facts

Interesting Facts about 2-Ethylphenanthrene

2-Ethylphenanthrene is a fascinating polycyclic aromatic hydrocarbon (PAH) that belongs to the family of phenanthrenes. Its unique structure and properties have garnered attention in various fields, including environmental chemistry and materials science.

Chemical Structure and Properties

  • Polycyclic Aromatic Hydrocarbon: 2-Ethylphenanthrene consists of three fused aromatic rings, making it a part of the larger group of PAHs that are known for their stability and hydrophobicity.
  • Source: This compound is commonly found in fossil fuels and can be a by-product of incomplete combustion, furthering the need for its study as an environmental pollutant.
  • Solubility: While many PAHs are insoluble in water, their behavior in organic solvents makes them of interest for extraction and analysis.

Health and Environmental Implications

Like many other PAHs, 2-ethylphenanthrene has raised concerns regarding its potential health effects. While extensive studies are ongoing, here are a few critical points to note:

  • Carcinogenicity: Some derivatives of PAHs are known to be carcinogenic, which highlights the importance of understanding the effects of exposure to this compound.
  • Environmental Monitoring: Monitoring levels of 2-ethylphenanthrene in environmental samples is crucial, as it may serve as an indicator of pollution from petrochemical sources.

Applications in Research

2-Ethylphenanthrene's structural properties make it a valuable compound for research purposes:

  • Analytical Chemistry: This compound is often used in studies related to the environmental persistence of PAHs and can serve as a marker in pollution analysis.
  • Material Science: Research is being conducted on the potential of PAHs, including 2-ethylphenanthrene, in developing new materials with enhanced properties.

As a compound, 2-ethylphenanthrene embodies the complexity of chemistry and its relevance to both environmental issues and material sciences. Continuous research into its implications and applications will shed light on both its challenges and potential benefits in various scientific domains.

Synonyms
Phenanthrene, 2-ethyl-
2-Ethyl-phenanthrene
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