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Avobenzone

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Identification
Molecular formula
C20H28O3
CAS number
70356-09-1
IUPAC name
1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one
State
State
At room temperature, Avobenzone is typically in a solid state, appearing as a powder.
Melting point (Celsius)
81.00
Melting point (Kelvin)
354.15
Boiling point (Celsius)
496.90
Boiling point (Kelvin)
770.05
General information
Molecular weight
310.44g/mol
Molar mass
310.4200g/mol
Density
1.0900g/cm3
Appearence

Avobenzone appears as a light yellow to white crystalline powder. It is commonly used in sunscreen formulations and is known for its oil-soluble nature.

Comment on solubility

Solubility of 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one

The solubility of 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one can be quite intriguing due to its unique structure and functional groups. Understanding its solubility can be essential for applications in pharmaceuticals, cosmetics, and other formulations. Here are some key points to consider:

  • Polarity: This compound features both hydrophobic (butoxy and hexanone) and hydrophilic (hydroxy) regions, indicating that its solubility may depend heavily on the solvent used.
  • Solvent Compatibility: It is expected to be soluble in organic solvents such as ethanol, acetone, and chloroform, which can effectively interact with its non-polar segments.
  • Water Solubility: Given the hydrophobic character of the butoxy and hexanone groups, it is likely to have limited solubility in water. However, the hydroxy group may enhance its partial solubility under certain conditions.
  • Temperature Effects: Solubility may increase with temperature, as is often the case with organic compounds, leading to a higher degree of molecular motion and potential interactions with solvent.
  • Concentration Influence: In concentrated solutions, intermolecular interactions among the solute molecules could also play a significant role, influencing overall solubility behavior.

Considering these factors, one can conclude that the solubility of 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one will be substantially dependent on both the solvent environment and the conditions under which it is being assessed. This complex interplay highlights the need for further experimental analysis to accurately gauge solubility in various scenarios.

Interesting facts

Exploring 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one

1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one is a fascinating compound with unique properties and applications. Here are some interesting facts:

  • Structure and Functionality: The compound features a hexanone backbone linked to a phenolic ring that contains both butoxy and hydroxy substituents. This provides it with distinct chemical behavior, particularly its ability to participate in various substitution reactions.
  • Applications: Compounds with similar structures often find utility in pharmaceuticals and agrochemicals. This particular compound could serve as a precursor for designing more complex molecules due to its versatility in organic synthesis.
  • Biological Relevance: Compounds incorporating a phenolic structure are frequently studied for their biological activities. Some phenolic compounds possess antioxidant properties and may be involved in protecting against oxidative stress.
  • Potential in Material Science: The presence of both hydroxy and butoxy groups could allow for interesting interactions with polymers, making this compound potentially useful in the development of new materials.

As a scientist or a student, exploring the behavior of 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one in various chemical environments can lead to innovative solutions in different fields of chemistry. Its unique structure opens the door for research into its reactivity, stability, and potential applications.

In summary, compounds like 1-(4-butoxy-2-hydroxy-phenyl)hexan-1-one are important not just for their inherent properties, but also for their potential to connect diverse areas of study. Engaging with such compounds can deepen our understanding of chemical interactions and drive advancements in science and technology.

Synonyms
HEXANOPHENONE, 4'-BUTOXY-2'-HYDROXY-
BRN 2271043
4'-Butoxy-2'-hydroxyhexanophenone
Capronylresorzin n-butylaether
Capronylresorzin n-butylaether [German]
19347-51-4
DTXSID10172949
DTXCID7095440
RefChem:347734
1-(4-butoxy-2-hydroxyphenyl)-1-hexanone