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4,6-bis(1-methylpentyl)benzene-1,3-diol

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Identification
Molecular formula
C18H30O2
CAS number
756-74-1
IUPAC name
4,6-bis(1-methylpentyl)benzene-1,3-diol
State
State

At room temperature, 4,6-bis(1-methylpentyl)benzene-1,3-diol is in a liquid state.

Melting point (Celsius)
19.50
Melting point (Kelvin)
292.70
Boiling point (Celsius)
352.40
Boiling point (Kelvin)
625.50
General information
Molecular weight
246.44g/mol
Molar mass
246.3700g/mol
Density
0.9950g/cm3
Appearence

The compound is typically a colorless liquid that may exhibit a slight yellow tint. It is often noted for its oily consistency.

Comment on solubility

Solubility of 4,6-bis(1-methylpentyl)benzene-1,3-diol

4,6-bis(1-methylpentyl)benzene-1,3-diol, a compound with intriguing structural features, exhibits interesting solubility characteristics. Understanding the solubility of this compound involves considering several factors:

  • Polar vs. Nonpolar Nature: The presence of multiple hydrocarbon (alkyl) chains often suggests a nonpolar character, making the compound less soluble in polar solvents like water.
  • Hydroxyl Groups: The -OH groups present in the structure can enhance solubility in polar environments to some extent due to hydrogen bonding capabilities.
  • Solvent Compatibility: This compound is likely to exhibit better solubility in nonpolar organic solvents such as hexane or toluene, while showing limited solubility in aqueous solutions.
  • Temperature Effects: As with many organic compounds, solubility can be influenced by temperature; higher temperatures may increase solubility in organic solvents.

In summary, while 4,6-bis(1-methylpentyl)benzene-1,3-diol may show limited solubility in water due to its predominant nonpolar characteristics, its solubility can be significantly enhanced in nonpolar organic solvents. Understanding its solubility behavior is essential for applications in various fields, including pharmaceuticals and material sciences.

Interesting facts

Interesting Facts about 4,6-bis(1-methylpentyl)benzene-1,3-diol

The compound 4,6-bis(1-methylpentyl)benzene-1,3-diol possesses fascinating properties and applications that intrigue chemists and students alike. Known primarily for its role as an important building block in organic synthesis, this molecule showcases versatility and efficacy in various domains.

Key Features

  • Structure and Stability: The unique arrangement of the benzene ring with two alkyl substituents contributes to the molecule's stability and reactivity, making it a critical component in synthetic organic chemistry.
  • Biological Activity: Research suggests that compounds similar to 4,6-bis(1-methylpentyl)benzene-1,3-diol may exhibit biological activities, including potential anti-inflammatory and antioxidant properties. This opens avenues for further exploration in medicinal chemistry.
  • Industrial Applications: Its derivatives are employed in the formulation of specialty chemicals, plastics, and even personal care products due to their properties that enhance performance and durability.

Chemical Relevance

Understanding the chemical properties of 4,6-bis(1-methylpentyl)benzene-1,3-diol is crucial for students and researchers engaged in:

  • Organic Synthesis: Serving as a reaction intermediate, it can undergo further modifications, leading to various functionalized compounds.
  • Material Science: Its derivatives play pivotal roles in developing advanced materials with tailored characteristics.
  • Pharmaceutical Research: By studying its biological interactions, chemists aim to create more effective therapeutic agents.

As a chemist observing the molecular world, one might reflect on the words of acclaimed scientist Linus Pauling: "The best way to have a good idea is to have lots of ideas." This sentiment applies well in the case of 4,6-bis(1-methylpentyl)benzene-1,3-diol, where its inherent complexities and potential applications invite numerous innovative thoughts within the field of chemistry.

Synonyms
4,6-di(hexan-2-yl)benzene-1,3-diol
17048-38-3
4,6-BIS(1-METHYLPENTYL)RESORCINOL
4,6-DIHEXAN-2-YLBENZENE-1,3-DIOL
0GEI7362XR
1,3-Benzenediol, 4,6-bis(1-methylpentyl)-
UNII-0GEI7362XR
Resorcinol, 4,6-bis(1-methylpentyl)-
SCHEMBL15378781
DTXSID80937769
1,3-DIHYDROXY-4,6-DI-SEC-HEXYLBENZENE
Q27236753