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Homosalate

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Identification
Molecular formula
C16H22O3
CAS number
118-56-9
IUPAC name
3-tert-butyl-2-hydroxy-6-methyl-benzoic acid
State
State

At room temperature, homosalate is in a liquid state. It is clear to slightly yellow and suitable as an active ingredient in cosmetic formulations.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.00
Boiling point (Celsius)
161.00
Boiling point (Kelvin)
434.00
General information
Molecular weight
262.35g/mol
Molar mass
262.3530g/mol
Density
1.0450g/cm3
Appearence

Homosalate is a liquid that ranges from being colorless to pale yellow. It is an organic compound that is often used in sunscreens for its ability to absorb ultraviolet light.

Comment on solubility

Solubility of 3-tert-butyl-2-hydroxy-6-methyl-benzoic acid

3-tert-butyl-2-hydroxy-6-methyl-benzoic acid, a complex aromatic compound, exhibits unique solubility characteristics influenced by its molecular structure. The presence of both hydrophobic and hydrophilic functional groups creates a balance that affects its dissolution in various solvents.

Key Factors Influencing Solubility:

  • Polar and Nonpolar Interactions: The hydroxyl group (-OH) is polar, potentially enhancing solubility in polar solvents like water, while the tert-butyl and methyl groups contribute to hydrophobicity.
  • pH Dependency: As a carboxylic acid, its acid-base behavior plays a role in solubility; at higher pH levels, deprotonation may lead to increased solubility in aqueous solutions.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature, allowing greater dissolution in both polar and nonpolar solvents.

In conclusion, while 3-tert-butyl-2-hydroxy-6-methyl-benzoic acid may have moderate aqueous solubility, its behavior can significantly vary depending on environmental conditions. As quoted from solubility studies, "the interplay of structure and environment is crucial in predicting solubility outcomes."

Interesting facts

Interesting Facts about 3-tert-butyl-2-hydroxy-6-methyl-benzoic acid

3-tert-butyl-2-hydroxy-6-methyl-benzoic acid, often referred to by its systematic name or simply as a derivative of benzoic acid, is a fascinating organic compound with various applications. Here are some interesting highlights:

  • Structural Diversity: This compound features a complex structure that combines a benzoic acid moiety with several functional groups, including a tert-butyl and hydroxyl group. The presence of these groups contributes to the compound's unique chemical properties.
  • Applications in Industry: 3-tert-butyl-2-hydroxy-6-methyl-benzoic acid is often studied for its potential applications in the field of materials science and pharmaceuticals. Its derivatives can be used as intermediates in syntheses.
  • Biological Activity: Research suggests that compounds with similar structures may exhibit interesting biological properties, including anti-inflammatory and antimicrobial activity. While specific studies on this compound may be limited, its structural relatives warrant investigation.
  • Environmental Impact: As with many organic compounds, it is crucial to consider the environmental impact of 3-tert-butyl-2-hydroxy-6-methyl-benzoic acid. Responsible usage and understanding its degradation pathways can contribute to better environmental management.

Understanding this compound is essential for both students and professionals, as it opens up a world of chemical reactivity and potential applications. As chemists continue to explore its properties, we may uncover even more exciting uses for this versatile compound.

Synonyms
3-tert-butyl-6-methylsalicylic acid
636-201-0
3-tert-butyl-2-hydroxy-6-methylbenzoic acid
6934-03-8
2,6-CRESOTIC ACID, 3-tert-BUTYL-
BRN 2581616
2-Methyl-5-tert-butylsalicylic acid
3-tert-Butyl-6-methylsalycilic acid
Salycilic acid, 3-tert-butyl-6-methyl-
CHEMBL250236
SCHEMBL1457176
DTXSID30219385
6-methyl-3-t-butylsalicylic acid
JXQCUCDXLSGQNZ-UHFFFAOYSA-N
ALBB-035111
AKOS005065475
3-tert. Butyl-6-methyl salicylic acid
FB68080
3-tert-butyl-2-hydroxy-6-methyl-benzoic acid
3-(tert-Butyl)-2-hydroxy-6-methylbenzoic acid
4-10-00-00752 (Beilstein Handbook Reference)