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4-Hexoxyphenol

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Identification
Molecular formula
C12H18O2
CAS number
55318-69-7
IUPAC name
4-hexoxyphenol
State
State

At room temperature, 4-Hexoxyphenol is typically a solid with crystalline form. It should be handled carefully to prevent exposure to moisture and light, which may affect its stability and appearance.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
307.50
Boiling point (Kelvin)
580.65
General information
Molecular weight
194.27g/mol
Molar mass
180.2430g/mol
Density
1.0529g/cm3
Appearence

4-Hexoxyphenol appears as an off-white to pale pink crystalline solid. It may darken upon exposure to air and light, which causes some impurity or degradation.

Comment on solubility

Solubility of 4-hexoxyphenol

4-hexoxyphenol, known for its unique structure and properties, exhibits interesting solubility characteristics. Below are some key points regarding its solubility:

  • Solvents: This compound is predominantly soluble in organic solvents such as ethanol, acetone, and ether, owing to its hydrophobic hexoxy group.
  • Water Solubility: 4-hexoxyphenol has limited solubility in water. This is primarily due to the non-polar hydrocarbon tail, which hinders its ability to form hydrogen bonds with water molecules.
  • Temperature Dependency: Like many organic compounds, the solubility of 4-hexoxyphenol can increase with temperature, which facilitates the breaking of intermolecular interactions.
  • pH Effects: The solubility may also be affected by the pH of the solution, as the ionization of phenolic compounds can occur under varying conditions.

In conclusion, while 4-hexoxyphenol demonstrates a strong affinity for non-polar solvents, its interaction with polar solvents like water is notably weaker. These solubility traits are critical for understanding its application in various fields, especially in organic synthesis and formulation chemistry.

Interesting facts

Interesting Facts about 4-Hexoxyphenol

4-Hexoxyphenol, an organic compound belonging to the phenol family, plays a significant role in various industrial applications and research. Here are some intriguing facts about this compound:

  • Structure: The molecular structure of 4-hexoxyphenol features a phenolic hydroxyl group attached to a hexoxy alkyl chain. This unique structure contributes to its interesting properties and reactivity.
  • Applications: 4-Hexoxyphenol is primarily used as an intermediate in the synthesis of various chemicals, including emulsifiers, surfactants, and antioxidants. It finds applications in industries such as cosmetics, food technology, and pharmaceuticals.
  • Biological Activity: Research has indicated that compounds related to 4-hexoxyphenol may exhibit antioxidant properties. These properties can be beneficial in preventing oxidative stress in biological systems.
  • Environmental Impact: As with many phenolic compounds, the environmental behavior of 4-hexoxyphenol is of interest to scientists. Understanding its degradation pathways and potential toxicological effects is important for assessing risks in ecological studies.
  • Safety Precautions: When handling 4-hexoxyphenol, it is crucial to adhere to safety protocols due to possible irritation effects on the skin and eyes. Always wear appropriate personal protective equipment (PPE) in laboratory environments.

In conclusion, 4-hexoxyphenol serves as an exciting example of how simple organic compounds can have versatile applications and important implications in both industry and environmental science. Its combination of structural features and potential functionalities makes it a subject worth further exploration in the realm of chemistry.

Synonyms
4-Hexyloxyphenol
4-(HEXYLOXY)PHENOL
Phenol, 4-(hexyloxy)-
4-n-Hexyloxyphenol
p-Hexyloxyphenol
UNII-35IMS9L1FE
35IMS9L1FE
DTXSID4048195
P-HEXOXYPHENOL
4-N-HEXOXYPHENOL
EINECS 242-713-1
4-(HEXYLOXY)BENZOLOL
PHENOL, P-(HEXYLOXY)-
DTXCID9028170
242-713-1
XIIIHRLCKLSYNH-UHFFFAOYSA-N
18979-55-0
4-hexoxyphenol
MFCD00002337
Hydroquinone Monohexyl Ether
CHEBI:34407
4-(Hexyloxy)phenol, 99%
SCHEMBL270164
CHEMBL225563
SCHEMBL2093109
SCHEMBL27396786
SCHEMBL27418496
SCHEMBL27612311
ALBB-025648
Tox21_303471
SBB059152
AKOS003382511
CS-W010645
NCGC00257244-01
SY048366
CAS-18979-55-0
H0439
NS00026201
ST45028664
D90871
EN300-7403785
12N-116
Q27116047