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5,11-Dimethylchrysene

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Identification
Molecular formula
C20H16
CAS number
73846-03-4
IUPAC name
5,11-dimethylchrysene
State
State

At room temperature, 5,11-Dimethylchrysene is in a solid state. It is a crystalline substance, which can be handled under standard laboratory conditions where it maintains its structural integrity without sublimation or significant phase change.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
402.00
Boiling point (Kelvin)
675.15
General information
Molecular weight
252.34g/mol
Molar mass
252.3390g/mol
Density
0.9450g/cm3
Appearence

5,11-Dimethylchrysene is a polycyclic aromatic hydrocarbon that appears as a pale yellow to orange crystalline solid. The compound is part of a group of substances formed by the fusion of several benzene rings, contributing to its aromatic character and distinct coloration.

Comment on solubility

Solubility of 5,11-dimethylchrysene

5,11-dimethylchrysene, a polycyclic aromatic hydrocarbon, exhibits unique solubility characteristics due to its structural properties. The solubility of this compound can be summarized as follows:

  • Nonpolar Characteristics: Being a nonpolar compound, 5,11-dimethylchrysene has a low affinity for polar solvents like water. Thus, it is practically insoluble in water.
  • Solubility in Organic Solvents: Conversely, it displays good solubility in nonpolar organic solvents such as:
    • Hexane
    • Benzene
    • Toluene
  • Temperature Effects: Solubility can be influenced by temperature; generally, an increase in temperature enhances solubility in organic solvents.

In summary, due to its distinct nonpolar nature, 5,11-dimethylchrysene is primarily soluble in nonpolar organic solvents and remains insoluble in polar solvents like water. This principle highlights the importance of "like dissolves like" in predicting solubility behavior.

Interesting facts

Interesting Facts about 5,11-Dimethylchrysene

5,11-Dimethylchrysene is a fascinating polycyclic aromatic hydrocarbon (PAH) that has garnered interest in various fields of science, particularly due to its structural and chemical properties. Here are some captivating insights:

  • Structural Complexity: With its intricate arrangement of carbon rings, 5,11-dimethylchrysene showcases a unique pattern of fusion between aromatic structures, making it a subject of interest in studies of molecular architecture.
  • Biological Impact: Studies suggest that PAHs, including 5,11-dimethylchrysene, can have significant effects on biological systems. They may exhibit mutagenic properties, which can lead to concerns regarding environmental pollution and human health.
  • Source of Interest: This compound is often found in products of incomplete combustion, like fossil fuels and tobacco smoke. Its presence in the environment raises questions about the long-term effects of exposure.
  • Research Applications: Chemists and environmental scientists are particularly interested in 5,11-dimethylchrysene in their quest to understand PAHs' behavior in ecological systems and develop remediation strategies for contaminated sites.

As a derivative of chrysene, 5,11-dimethylchrysene also serves as a model compound in theoretical studies related to organic chemistry and materials science. With its complex bonding structure and interaction capabilities, it assists in exploring the synthesis of new materials and understanding organic reaction mechanisms.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." The study of compounds like 5,11-dimethylchrysene exemplifies this notion, as it opens the door to new discoveries and innovations in chemistry.

Synonyms
5,11-Dimethylchrysene
14207-78-4
DTXSID50161938
DTXCID1084429
BRN 2105855
CHRYSENE, 5,11-DIMETHYL-
CHEMBL3230486