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3-Methyl-1H-benzo[c]phenanthrene

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Identification
Molecular formula
C19H14
CAS number
243-02-5
IUPAC name
3-methylbenzo[c]phenanthrene
State
State

At room temperature, 3-methylbenzo[c]phenanthrene exists as a solid.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
254.32g/mol
Molar mass
254.3230g/mol
Density
1.2000g/cm3
Appearence

3-Methylbenzo[c]phenanthrene is an organic compound that typically appears as a pale yellow crystalline solid. Due to its polycyclic aromatic hydrocarbon structure, it often forms shiny, platelet-like crystals when purified.

Comment on solubility

Solubility of 3-methylbenzo[c]phenanthrene

3-methylbenzophenanthrene is a polycyclic aromatic hydrocarbon (PAH) known for its complex structure, which significantly influences its solubility characteristics. Here are some key points regarding its solubility:

  • Hydrophobic Nature: Due to its extensive aromatic system, 3-methylbenzophenanthrene demonstrates a strong hydrophobic effect. This leads to low solubility in polar solvents such as water.
  • Solubility in Organic Solvents: The compound is more soluble in non-polar organic solvents like:
    • Hexane
    • Chloroform
    • Toluene
  • Temperature Influence: The solubility of 3-methylbenzophenanthrene can also be affected by temperature, as increased temperatures often result in enhanced solubility in organic solvents.
  • Applications: Understanding its solubility is crucial for its applications in fields such as environmental science and material chemistry.

In summary, the solubility of 3-methylbenzophenanthrene varies significantly depending on the solvent and environmental conditions, showing particularly low affinity for water while being well-dissolved in various organic solvents.

Interesting facts

Interesting Facts about 3-methylbenzophenanthrene

3-methylbenzophenanthrene is a fascinating polycyclic aromatic hydrocarbon (PAH) that draws attention for both its structure and its implications in environmental science. Here are some compelling aspects of this compound:

  • Structural Complexity: This compound consists of four fused aromatic rings, which contributes to its stability and unique chemical behavior. The methyl group attached to the benzo structure plays a critical role in its reactivity and interaction with other chemicals.
  • Environmental Relevance: As a member of the PAH family, 3-methylbenzophenanthrene is often found in fossil fuels and can arise from incomplete combustion processes. This gives it a notable presence in environmental studies, particularly related to air and soil pollution.
  • Health Concerns: Polycyclic aromatic hydrocarbons, including 3-methylbenzophenanthrene, have raised concerns regarding their carcinogenic potential. Research suggests that exposure to PAHs may be linked to various health issues, making this compound a subject of interest in toxicology.
  • Research Applications: Scientists utilize this compound to explore various aspects of organic chemistry, including reaction mechanisms and the effects of substituents in complex hydrocarbon systems. Its structure allows for investigating the dynamics of molecular interactions.
  • Natural Sources: 3-methylbenzophenanthrene can be naturally produced through the degradation of organic matter in different environments, which presents insights into biogeochemical cycles.

In summary, 3-methylbenzophenanthrene serves as a prime example of how complex organic compounds can influence both human health and the environment, making its study crucial for advancing our understanding of chemical science.

Synonyms
3-Methylbenzo[c]phenanthrene
3-Methylbenzo(c)phenanthrene
2381-19-3
3-Methyl-3,4-benzophenanthrene
7-Methyl-3:4-benzophenanthrene
7-Methyl-3,4-benzphenanthrene
Benzo[c]phenanthrene, 3-methyl-
QK9NBX92AZ
BENZO(c)PHENANTHRENE, 3-METHYL-
NSC-97698
NSC 97698
BRN 2328896
NSC97698
UNII-QK9NBX92AZ
Methylbenzo(c)phenanthrene
7-Methyl-3,4-benzphenanthren
DTXSID10946607
HFBPJADWYSMWGU-UHFFFAOYSA-N
WLN: L C6 B666J F1
AKOS024341213
78328-47-9