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Salicyl benzoate

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Identification
Molecular formula
C13H10O3
CAS number
118-55-8
IUPAC name
(3-hydroxyphenyl) benzoate
State
State

Salicyl benzoate is typically found in a solid state at room temperature. It can be handled as a crystalline powder in laboratory or industrial settings.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
212.21g/mol
Molar mass
212.2140g/mol
Density
1.2890g/cm3
Appearence

Salicyl benzoate appears as a white crystalline solid. It is often observed in its pure form as a powder.

Comment on solubility

Solubility of (3-Hydroxyphenyl) Benzoate

(3-Hydroxyphenyl) benzoate, a compound featuring both a hydroxy and a benzoate functional group, exhibits interesting solubility characteristics influenced largely by its molecular structure.


Factors Affecting Solubility:

  • Polarity: The presence of the hydroxy group enhances polarity, allowing for improved interaction with polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to the hydroxy group increases its solubility in polar solvent environments.
  • Hydrophobic Interactions: However, the hydrophobic benzoate moiety may reduce solubility in highly polar solvents, making it more soluble in organic solvents like ethanol or acetone.

To summarize, the solubility of (3-hydroxyphenyl) benzoate can be described as:

  • Soluble in polar solvents: Water (to some extent)
  • More soluble in organic solvents: Ethanol, acetone
  • Less soluble in non-polar solvents

The intricate balance between polar and non-polar characteristics leads to a moderate level of solubility, dictated by solvent choice. Thus, understanding the solubility of (3-hydroxyphenyl) benzoate is crucial for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts About (3-hydroxyphenyl) benzoate

(3-hydroxyphenyl) benzoate is a fascinating compound that merges the properties of both a hydroxyphenyl group and a benzoate moiety, offering unique chemical and physical characteristics.

Key Features

  • Dual Functionality: This compound presents a functional hydroxyl group which can participate in various chemical reactions, enhancing its reactivity in organic synthesis.
  • Applications in Research: (3-hydroxyphenyl) benzoate has been studied for its potential use in pharmaceuticals, as well as in the development of advanced materials due to its ability to change properties when exposed to different conditions.
  • Impact on Biological Systems: Compounds related to benzoates have been researched for their roles in metabolic pathways, making them crucial in understanding biochemical processes.

Scientific Insights

One notable aspect of (3-hydroxyphenyl) benzoate is its potential antioxidant properties. Antioxidants are essential in the fight against oxidative stress, which is linked to various diseases. The hydroxy group may contribute to its ability to neutralize free radicals, making it a subject of study for health-related applications.

Furthermore, the alignment of the hydroxyl and benzoate groups opens pathways for intermolecular interactions, influencing the compound's solubility and stability in different environments. This positional orientation can be crucial in designing experiments in material science and organic chemistry.

Conclusion

In summary, (3-hydroxyphenyl) benzoate exemplifies the interesting interplay between structure and function in organic compounds, making it a valuable compound for both academic research and practical applications in various fields.

Synonyms
3-Hydroxyphenyl benzoate
Resorcinol monobenzoate
136-36-7
1,3-Benzenediol, monobenzoate
Eastman Inhibitor RMB
(3-hydroxyphenyl) benzoate
RESORCINOL, MONOBENZOATE
Benzoic acid, m-hydroxyphenyl ester
3-BENZOYLOXYPHENOL
m-hydroxyphenyl benzoate
Benzoic Acid 3-Hydroxyphenyl Ester
NSC 4807
EINECS 205-241-7
1,3-Benzenediol, 1-benzoate
BRN 1873897
942E82KUWD
NSC-4807
RESORCINOL, BENZOATE
DTXSID1038878
1,3-BENZENEDIOL BENZOATE
CHEBI:156556
UNII-942E82KUWD
Resorcinol benzoate
MFCD00020118
WLN: QR COVR
SCHEMBL78117
Benzoic acid resorcinol ester
BIDD:ER0042
Resorcinol monobenzoate, 97%
CHEMBL2260450
DTXCID9018878
NSC4807
ALBB-025059
benzoic acid (3-hydroxyphenyl) ester
AKOS015839082
FH61997
DS-020848
B0077
CS-0308088
H1560
NS00024422
D88598
EN300-107171
Q27271634
Benzoic Acid 3-Hydroxyphenyl Ester;Resorcinol Monobenzoate
205-241-7