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Retene

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Identification
Molecular formula
C18H18
CAS number
483-65-8
IUPAC name
1,2,3-trimethyl-4-prop-1-enyl-naphthalene
State
State

Retene is typically found in the solid state at room temperature. It forms crystals that may vary in size depending on the method of preparation. As a member of the PAH family, it is typically stable under normal conditions.

Melting point (Celsius)
98.00
Melting point (Kelvin)
371.20
Boiling point (Celsius)
390.50
Boiling point (Kelvin)
663.60
General information
Molecular weight
234.35g/mol
Molar mass
234.3610g/mol
Density
0.9650g/cm3
Appearence

Retene typically appears as a colorless solid under standard conditions. It can also present as white crystals. Retene is known for its aromatic properties due to its structure consisting of a naphthalene nucleus substituted with methyl and propylene groups, contributing to a sweet and woody odor.

Comment on solubility

Solubility of 1,2,3-trimethyl-4-prop-1-enyl-naphthalene

1,2,3-trimethyl-4-prop-1-enyl-naphthalene, a complex organic compound, exhibits solubility characteristics that are important to consider for both laboratory and industrial applications. This compound, being a naphthalene derivative, is primarily non-polar, which influences its solubility profile significantly. Here are key points regarding its solubility:

  • Solubility in Organic Solvents: It displays good solubility in non-polar solvents such as hexane, benzene, and toluene. This is attributed to the hydrophobic interactions facilitated by its aromatic structure.
  • Limited Water Solubility: 1,2,3-trimethyl-4-prop-1-enyl-naphthalene is generally considered insoluble in water. The high molecular weight and non-polar nature prevent effective interaction with polar water molecules.
  • Temperature Influence: Solubility may be affected by temperature; higher temperatures can increase the solubility of organic compounds in solvents by enhancing molecular motion.
  • Applications: Its solubility characteristics make it valuable in processes where non-polar solvents are employed, such as in oil and fragrance formulations.

In conclusion, understanding the solubility of 1,2,3-trimethyl-4-prop-1-enyl-naphthalene is crucial for optimizing its use in various applications, as it underscores the importance of compatibility with solvents and the challenges posed by water interaction.

Interesting facts

Interesting Facts about 1,2,3-trimethyl-4-prop-1-enyl-naphthalene

1,2,3-trimethyl-4-prop-1-enyl-naphthalene, a fascinating compound in the family of polycyclic aromatic hydrocarbons, boasts a rich array of characteristics that make it a subject of interest in organic chemistry and natural product synthesis. Here are some engaging insights about this unique compound:

  • Chemical Structure: The compound features a naphthalene backbone, known for its two fused aromatic rings, enhancing its stability and reactivity.
  • Natural Occurrence: Similar compounds are often found in various essential oils and are noted for their fragrance, playing a significant role in perfumery and flavoring industries.
  • Biological Activity: Some derivatives of naphthalene compounds have shown promising biological properties, including antibacterial and antifungal activities, making them of interest in pharmaceutical research.
  • Industrial Applications: Its derivatives are vital in the synthesis of synthetic dyes and as intermediates in the production of various chemicals, highlighting its utility in industrial contexts.
  • Environmental Impact: Like many polycyclic aromatic hydrocarbons, understanding its behavior in the environment is crucial due to potential toxicity and persistence in ecosystems.

As a member of the extensive naphthalene family, 1,2,3-trimethyl-4-prop-1-enyl-naphthalene reflects the complexity and beauty inherent in organic chemistry. It serves as a reminder of the intricate relationships between structure and function in chemical compounds. As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." Exploring such compounds invites an abundance of possibilities in scientific research.

Synonyms
SCHEMBL27559080
1,2,3-trimethyl-4-propenyl-naphthalene
Naphthalene, 1,2,3-trimethyl-4-(1E)-1-propen-1-yl-