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1-Phenylethyl propionate

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Identification
Molecular formula
C12H16O2
CAS number
122-70-3
IUPAC name
1-phenylethyl propanoate
State
State

At room temperature, 1-Phenylethyl propionate is in a liquid state.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
238.50
Boiling point (Kelvin)
511.60
General information
Molecular weight
178.24g/mol
Molar mass
178.2430g/mol
Density
1.0090g/cm3
Appearence

1-Phenylethyl propionate is a colorless liquid with a characteristic fruity odor. It is often used in fragrances and flavorings to impart a sweet, floral, and fruity note.

Comment on solubility

Solubility of 1-Phenylethyl Propanoate

1-Phenylethyl propanoate, with the chemical formula C12H16O2, exhibits interesting solubility characteristics due to its structural features.

Regarding its solubility, consider the following points:

  • Polarity: 1-Phenylethyl propanoate is a relatively non-polar compound. This affects its interaction with solvents.
  • Solvent Compatibility: It tends to be soluble in organic solvents such as:
    • Ethyl acetate
    • Toluene
    • Chloroform
  • Poor Water Solubility: Due to its non-polar nature, it has poor solubility in water. This can be attributed to the lack of strong hydrogen bonding capabilities.
  • Temperature Dependence: Solubility can vary with temperature; increasing temperatures generally lead to higher solubility in organic solvents.

Overall, understanding the solubility of 1-phenylethyl propanoate is crucial for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 1-Phenylethyl Propanoate

1-Phenylethyl propanoate, also known as benzyl propanoate, is an organic compound that belongs to the category of esters. This compound is not just a simple molecule; it has fascinating applications and characteristics:

  • Esters in Flavor and Fragrance: 1-Phenylethyl propanoate is often used in the production of fragrances and flavorings. Its pleasant aroma contributes to the formulation of perfumes and food additives, making it a valued compound in the cosmetic and culinary industries.
  • Synthesis and Reactions: This compound can be synthesized through the esterification process, where phenylethanol reacts with propanoic acid in the presence of an acid catalyst. This reaction is a classic example of how simple alcohols and acids can create delightful aromas.
  • Biological Activity: Some studies have indicated that compounds related to 1-phenylethyl propanoate might possess biological activities, such as antimicrobial properties. This opens avenues for exploring its potential use in medicine.
  • Chiral Nature: Interestingly, 1-phenylethyl propanoate is derived from a chiral alcohol, which means that its synthesis can lead to different enantiomers. This property is crucial in the field of asymmetric synthesis, where the configuration of molecules can influence their biological effects.
  • Use in the Aroma Industry: Besides its use in food, 1-phenylethyl propanoate is highly prized in the aroma industry for its ability to create complex scent profiles, making it a common choice for scented products.

In summary, 1-phenylethyl propanoate is more than just a chemical compound; it plays significant roles in various fields. As scientists and students of chemistry continue to explore the possibilities of this ester, its contributions to aroma, flavoring, and potential medicinal uses reflect the fascinating interconnections among chemistry, biology, and industry.

Synonyms
1-Phenylethyl propionate
120-45-6
1-phenylethyl propanoate
Styrallyl propionate
Styralyl propionate
Methylphenylcarbinyl propionate
alpha-Methylbenzyl propionate
Phenylmethylcarbinyl propionate
Benzenemethanol, alpha-methyl-, 1-propanoate
alpha-Methylbenzyl propanoate
1-Phenyl-1-ethyl propionate
FEMA No. 2689
alpha-Methylbenzyl alcohol, propionate
Styrolyl propionate
alpha-Methylbenzenemethanol propanoate
.alpha.-Methylbenzyl propionate
NSC 406571
Propionic acid, alpha-methylbenzyl ester
Benzenemethanol, alpha-methyl-, propanoate
EINECS 204-397-3
Benzenemethanol, .alpha.-methyl-, propanoate
J5A62A7WWF
BENZYL ALCOHOL, alpha-METHYL-, PROPIONATE
BRN 1948418
DTXSID9047091
AI3-04100
NSC-406571
Benzyl alcohol, .alpha.-methyl-, propionate
DTXCID7027091
3-06-00-01680 (Beilstein Handbook Reference)
(+/-)-1-PHENYLETHYL PROPIONATE
1-PHENYLETHANOL PROPIONIC ACID ESTER
.ALPHA.-METHYLBENZYL PROPIONATE [FHFI]
Benzenemethanol, .alpha.-methyl-, 1-propanoate
UNII-J5A62A7WWF
styrolylpropionat
MFCD00009305
1-phenylethylpropionate
SCHEMBL538486
.alpha.-Methylbenzyl propanoate
CHEMBL3185936
FEMA 2689
CHEBI:173831
propionic acid 1-phenyl-ethyl ester
Tox21_302346
NSC406571
AKOS015912978
CS-W017314
HY-W016598
.alpha.-Methylbenzyl alcohol, propionate
NCGC00256024-01
alpha-Methylbenzyl propionate, >98%, FG
AS-64763
CAS-120-45-6
Benzenemethanol, |A-methyl-, 1-propanoate
Propionic acid, .alpha.-methylbenzyl ester
NS00013193
Q27891219
204-397-3