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1,3,6-trimethylnaphthalene

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Identification
Molecular formula
C13H14
CAS number
829-26-5
IUPAC name
1,3,6-trimethylnaphthalene
State
State
Liquid at room temperature. It is a volatile organic compound and exists as a liquid under ambient conditions.
Melting point (Celsius)
16.00
Melting point (Kelvin)
289.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
172.26g/mol
Molar mass
172.2640g/mol
Density
0.9975g/cm3
Appearence

1,3,6-Trimethylnaphthalene is a colorless liquid with an aromatic odor. It is clear and lacks any solid particulates or significant color.

Comment on solubility

Solubility of 1,3,6-trimethylnaphthalene

1,3,6-trimethylnaphthalene, with the chemical formula C15H12, is an organic compound that exhibits unique solubility characteristics. As an aromatic hydrocarbon, it is largely non-polar, which significantly influences its solubility in various solvents.

Key points about the solubility of this compound include:

  • Solubility in Organic Solvents: 1,3,6-trimethylnaphthalene is generally soluble in non-polar organic solvents such as toluene, hexane, and benzene. This is due to the similar polarity between the compound and these solvents.
  • Poor Water Solubility: Conversely, it is insoluble in water. This is typical for non-polar compounds, as they cannot effectively interact with the polar water molecules.
  • Temperature Influence: The solubility of 1,3,6-trimethylnaphthalene may also be affected by temperature, with higher temperatures generally improving solubility in organic media.

In summary, the solubility behavior of 1,3,6-trimethylnaphthalene reflects its non-polar nature, making it well-suited for uses in non-polar environments but limiting its application in aqueous solutions. As always, understanding these solubility traits is crucial for its practical applications in various fields.

Interesting facts

Interesting Facts About 1,3,6-Trimethylnaphthalene

1,3,6-Trimethylnaphthalene is a fascinating organic compound that belongs to the naphthalene family, showcasing the depth and complexity of aromatic hydrocarbons. Here are some engaging insights:

  • Aromatic Structure: This compound features a naphthalene base, which consists of two fused benzene rings, resulting in a *highly stable* aromatic structure that is a hallmark of many organic compounds.
  • Isomeric Diversity: As a trimethyl-substituted derivative of naphthalene, it exists alongside several isomers that offer unique properties and reactivity, contributing to its application in various chemical syntheses.
  • Source of Energy: 1,3,6-Trimethylnaphthalene is often studied in the context of *fuel additives* due to its potential to alter combustion characteristics and improve the efficiency of hydrocarbon fuels.
  • Research Applications: Its derivatives and related compounds are of great interest in *polymer synthesis* and materials science, often serving as precursors to valuable polymers and functionalized materials.
  • Natural Occurrence: This compound can be found in *coal tar* and various crude oil fractions, making it a substance of interest for studies related to fossil fuels and environmental chemistry.
  • Health and Safety: As with many hydrocarbons, handling 1,3,6-trimethylnaphthalene requires a keen understanding of safety protocols, especially considering its volatility and potential environmental impact.

In conclusion, the study of 1,3,6-trimethylnaphthalene not only extends our understanding of aromatic compounds but also has practical implications in fuel technology and materials science, emphasizing the *interconnectedness* of chemistry and its applications in our everyday lives.

Synonyms
1,3,6-TRIMETHYLNAPHTHALENE
3031-08-1
UKN0OLK7RS
Naphthalene, 1,3,6-trimethyl-
EINECS 221-205-3
UNII-UKN0OLK7RS
DTXSID00184399
AKOS006279702
NS00047082
Q27291120