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Octocrylene

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Identification
Molecular formula
C24H27NO2
CAS number
6197-30-4
IUPAC name
[4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone
State
State
Octocrylene is typically in a liquid state at room temperature. It is often incorporated into cosmetic formulations due to its stability and efficacy as a UV filter.
Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
361.48g/mol
Molar mass
361.4800g/mol
Density
1.0509g/cm3
Appearence
Octocrylene appears as a clear, colorless, and viscous liquid. It is commonly used in the formulation of sunscreens and other cosmetic products. The compound is known for its ability to absorb UVB and short-wave UVA rays, adding photostability to these products.
Comment on solubility

Solubility of [4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone

The solubility of [4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone is a topic of keen interest in both industrial and laboratory settings. Understanding the solubility characteristics of this compound helps in various applications such as formulation and processing. Here are some key considerations:

  • Polar vs. Nonpolar: The structure of this compound contains both hydrophobic (nonpolar) and hydrophilic (polar) regions due to the presence of the phenolic groups and the long aliphatic chain. This dual nature suggests that it may exhibit moderate solubility in organic solvents but limited solubility in water.
  • Solvent Selection: Common organic solvents like ethanol and acetone could effectively dissolve this compound, thanks to their polar and nonpolar characteristics which can accommodate the molecule’s complex structure.
  • Temperature Influence: As with many organic compounds, the solubility may increase with temperature, allowing the compound to dissolve more readily in heated solvents.
  • Application Relevance: Poor solubility in water means that this compound may be better suited for applications in non-aqueous environments, such as in organic coatings or as a photoinitiator in plastics.

In summary, while [4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone demonstrates moderate solubility properties, practical applications often depend on understanding these solubility dynamics thoroughly. This makes solvent choice, temperature, and the intended use critical components in its effective application.

Interesting facts

Interesting Facts about [4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone

[4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone, also known for its intricate structure and unique properties, belongs to a class of compounds known as ketones. This particular compound has garnered attention in various scientific fields, particularly in organic chemistry and materials science. Here are some intriguing aspects about this compound:

  • Versatile Applications: Due to its functional groups, this compound is relevant in several industries, including pharmaceuticals, where it may serve as a precursor for synthesizing more complex molecules.
  • Photochemical Properties: The phenyl groups in this structure contribute to interesting optical properties, making it a candidate for studies involving light absorption and emission.
  • Solvent Capabilities: The presence of the ethylhexoxy group enhances its solubility in organic solvents, which can influence its behavior in various reactions and applications.
  • Structure-Activity Relationship (SAR): Enthusiastic chemists leverage the versatility of its hydroxyl group, which can alter its reactivity, making it a subject of research for therapeutic efficacy in medicinal chemistry.

In the words of renowned chemist Richard Feynman, “What I cannot create, I do not understand.” Understanding the synthesis and behaviors of compounds like [4-(2-ethylhexoxy)-2-hydroxy-phenyl]-phenyl-methanone deepens our comprehension of chemical interactions and innovation.

Moreover, this compound's unique characteristics offer a pathway to explore sustainability in chemical processes, aligning with contemporary research goals aimed at reducing environmental impact through greener chemistry.

Synonyms
2549-90-8
3UET5R68HV
UVINUL-408
BENZOPHENONE, 4-(2-ETHYLHEXYLOXY)-2-HYDROXY-
(4-((2-Ethylhexyl)oxy)-2-hydroxyphenyl)phenylmethanone
2-HYDROXY-4-((2-ETHYLHEXYL)OXY)BENZOPHENONE
METHANONE, (4-((2-ETHYLHEXYL)OXY)-2-HYDROXYPHENYL)PHENYL-
[4-[(2-Ethylhexyl)oxy]-2-hydroxyphenyl]phenylmethanone
4-(2-Ethylhexyloxy)-2-hydroxybenzophenone
Methanone,[4-[(2-ethylhexyl)oxy]-2-hydroxyphenyl]phenyl-
[4-(2-ethylhexoxy)-2-hydroxyphenyl]-phenylmethanone
(4-((2-ethylhexyl)oxy)-2-hydroxyphenyl)(phenyl)methanone
BRN 1886814
{4-[(2-Ethylhexyl)oxy]-2-hydroxyphenyl}(phenyl)methanone
UF-5
2-Hydroxy-4-(2'-ethylhexoxy)benzofenon [Czech]
4-(2-Ethylhexyloxy)-2-hydroxybenzofenon [Czech]
2-Hydroxy-4-(2'-ethylhexoxy)benzofenon
4-(2-Ethylhexyloxy)-2-hydroxybenzofenon
UNII-3UET5R68HV
SCHEMBL534051
DTXSID50948382
SLXIKWJMGICOAO-UHFFFAOYSA-N