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Phenyl benzoate

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Identification
Molecular formula
C13H10O2
CAS number
93-99-0
IUPAC name
phenyl benzoate
State
State

At room temperature, phenyl benzoate is a solid.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
198.22g/mol
Molar mass
198.2210g/mol
Density
1.1998g/cm3
Appearence

Phenyl benzoate appears as a colorless, crystalline solid.

Comment on solubility

Solubility of Phenyl Benzoate

Phemyl benzoate, with the chemical formula C13H10O2, displays notable solubility characteristics that are intriguing for chemists and industrial applications.

Solubility in Various Solvents

Phenyl benzoate is generally considered to be:

  • Soluble in organic solvents such as:
    • Ether
    • Benzene
    • Toluene
    • Chloroform
  • Practically insoluble in water, which can be attributed to its non-polar characteristics and the difficulty of forming hydrogen bonds with water molecules.

Factors Influencing Solubility

Several factors can influence the solubility of phenyl benzoate:

  • Temperature: An increase in temperature can enhance the solubility of phenyl benzoate in organic solvents.
  • Polarity of Solvent: The non-polar nature of phenyl benzoate makes it more soluble in non-polar solvents and less so in polar solvents like water.
  • Presence of Other Solutes: The introduction of other solutes may affect the overall solubility dynamics.

In summary, while phenyl benzoate showcases versatility in organic solvents, its low solubility in water highlights the importance of solvent selection for various chemical applications. This compound serves as a perfect example of how molecular structure can dictate solubility, emphasizing the principle of "like dissolves like."

Interesting facts

Interesting Facts About Phenyl Benzoate

Pendeleon benzoate is an intriguing compound that embodies both simplicity and complexity in its structure and uses. This compound, which is an ester formed from phenol and benzoic acid, is notable for several reasons:

  • Historical Context: The synthesis of esters dates back to the early 19th century, marking a pivotal moment in organic chemistry. Phenyl benzoate is part of a broader family of esters that have evolved to play significant roles in both synthetic and natural processes.
  • Applications: This compound is utilized in various applications, including:
    • As a fragrance component in perfumes
    • In the formulation of certain cosmetics
    • As a plasticizer in the production of plastics, enhancing flexibility and durability
  • Biochemical Interest: Phenyl benzoate has been studied for its potential roles in biochemistry, particularly regarding its interactions with biological membranes and potential medicinal properties.
  • Analytical Relevance: This compound serves as a useful reagent in various chemical analyses and synthesis reactions, making it an essential subject for understanding ester chemistry.
  • Cultural Impact: In modern contexts, phenyl benzoate appears in numerous products we take for granted, from industrial items to everyday consumer goods, showcasing the importance of esters in society.

With its versatile properties and significance in various fields including chemistry, biochemistry, and industrial applications, phenyl benzoate remains an exciting compound for study and practical application. As with many chemical compounds, understanding its properties and uses helps us appreciate the intricate web of interactions that define both nature and technology.

Synonyms
PHENYL BENZOATE
93-99-2
Benzoic acid phenyl ester
Diphenylcarboxylate
Benzoic acid, phenyl ester
Phenol, benzoate
EINECS 202-293-2
UNII-B8A3WVZ590
MFCD00003072
NSC 37086
BRN 1566346
B8A3WVZ590
MLS002608016
DTXSID0048210
CHEBI:86919
AI3-04731
NSC-37086
DTXCID8028185
4-09-00-00303 (Beilstein Handbook Reference)
DPCate
CAS-93-99-2
PHENY L BENZOATE
Phenyl benzoate, 99%
WLN: RVOR
Benzoic acid-phenyl ester
bmse010254
SCHEMBL31888
PHENYL BENZOATE [MI]
CHEMBL1885870
MSK3407
HMS3080D03
NSC37086
Tox21_202880
Tox21_303595
AKOS001445255
CS-W010539
HY-W009823
NCGC00257480-01
NCGC00260426-01
AC-21023
DA-56799
SMR001526772
SY012912
B0075
NS00013974
EN300-82943
Q27159286
Z28228413
202-293-2
InChI=1/C13H10O2/c14-13(11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10