Skip to main content

1,6,7-trimethylnaphthalene

ADVERTISEMENT
Identification
Molecular formula
C13H14
CAS number
38362-16-0
IUPAC name
1,6,7-trimethylnaphthalene
State
State
At room temperature, the compound is typically in a liquid state.
Melting point (Celsius)
22.00
Melting point (Kelvin)
295.15
Boiling point (Celsius)
256.00
Boiling point (Kelvin)
529.15
General information
Molecular weight
170.27g/mol
Molar mass
170.2700g/mol
Density
0.9976g/cm3
Appearence

1,6,7-Trimethylnaphthalene appears as a colorless to pale yellow liquid. It exhibits a characteristic aromatic odor typical of naphthalene derivatives.

Comment on solubility

Solubility of 1,6,7-trimethylnaphthalene

1,6,7-trimethylnaphthalene is an organic compound derived from naphthalene, and its solubility characteristics are noteworthy.

This compound is largely insoluble in water due to its non-polar hydrocarbon structure. However, it exhibits varying solubility in different organic solvents. Here are some important points regarding its solubility:

  • Non-polar Solvents: 1,6,7-trimethylnaphthalene is readily soluble in non-polar solvents such as hexane and toluene.
  • Polar Solvents: It shows poor solubility in polar solvents like ethanol and acetone.
  • Hydrophobic Nature: The compound’s hydrophobic character contributes to its limited interaction with polar solvent molecules.
  • Temperature Sensitivity: Like many organic compounds, solubility may increase with temperature, hence it can be more soluble at elevated temperatures.

In summary, while 1,6,7-trimethylnaphthalene is highly insoluble in water, it can dissolve effectively in various non-polar organic solvents, highlighting the significance of solvent choice in chemical processes involving this compound. As with many hydrocarbons, the principle of "like dissolves like" holds true; thus, non-polar solvents are the preferred medium for its dissolution.

Interesting facts

Interesting Facts about 1,6,7-Trimethylnaphthalene

1,6,7-trimethylnaphthalene is a fascinating organic compound that belongs to the family of polycyclic aromatic hydrocarbons (PAHs). Its unique structure and properties make it a topic of interest in various fields of scientific research. Here are some intriguing aspects of this compound:

  • Structure and Isomerism: This compound features a naphthalene backbone with three methyl groups attached at the 1, 6, and 7 positions, which contributes to its distinctive molecular structure. The arrangement of methyl groups offers several isomeric forms, leading to interesting variations in chemical behavior.
  • Source and Natural Occurrence: 1,6,7-trimethylnaphthalene can be found in fossil fuels and products derived from oil refining, such as creosote. Its presence in these materials makes it relevant for environmental studies and assessments of pollution.
  • Applications: This compound has potential applications in the synthesis of dyes, pharmaceuticals, and agrochemicals, showcasing its versatility in the chemical industry. Scientists are actively exploring its use in the development of advanced materials.
  • Toxicology and Environmental Impact: As a member of the PAH family, 1,6,7-trimethylnaphthalene raises concerns regarding its environmental persistence and potential toxicity. Research into its ecological effects is essential for understanding risks associated with exposure.
  • Spectroscopy: Its unique functional groups and structure lead to distinctive spectral features that can be studied using techniques such as NMR and IR spectroscopy. These techniques help chemists identify and analyze compounds in complex mixtures.

As quoted by a renowned chemist, “Understanding the structure-activity relationship of compounds like 1,6,7-trimethylnaphthalene can unlock doors to innovative solutions in chemistry.” This highlights the compound's importance in both research and practical applications.

In summary, 1,6,7-trimethylnaphthalene stands as a prime example of the intricate connections within organic chemistry. Its diverse properties and potential uses continue to inspire scientific inquiry and innovation.

Synonyms
1,6,7-TRIMETHYLNAPHTHALENE
2245-38-7
2,3,5-Trimethylnaphthalene
UNII-4WC055TBJ9
4WC055TBJ9
EINECS 218-833-5
NSC 89511
NSC-89511
AI3-28792
DTXSID7062291
DTXCID1036703
Naphthalene, 1,6,7-trimethyl-(8CI)
Naphthalene, 1,6,7-trimethyl-(8CI)(9CI)
218-833-5
jbxulkrnhaqmas-uhfffaoysa-n
Naphthalene, 1,6,7-trimethyl-
Naphthalene, 2,3,5-trimethyl-
2,3,5-Trimethylnaphthalene 10 microg/mL in Cyclohexane
NSC89511
MFCD00044834
2,5-Trimethylnaphthalene
Naphthalene,3,5-trimethyl-
Naphthalene,6,7-trimethyl-
CHEBI:89809
AKOS006228565
AS-58800
DB-045926
CS-0320661
NS00027190
T0772
D78423
Q27161997