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4-Phenylbutanal

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Identification
Molecular formula
C10H12O
CAS number
5728-18-3
IUPAC name
4-phenylbutanal
State
State
At room temperature, 4-Phenylbutanal is typically in a liquid state. It is not a solid or a gas under standard conditions.
Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
231.00
Boiling point (Kelvin)
504.15
General information
Molecular weight
134.18g/mol
Molar mass
134.1790g/mol
Density
0.9881g/cm3
Appearence

4-Phenylbutanal appears as a clear, colorless to light yellow liquid. It has an aromatic odor that can be described as floral or sweet, making it sometimes used in the fragrance industry.

Comment on solubility

Solubility of 4-phenylbutanal

When considering the solubility of 4-phenylbutanal, various factors come into play due to its organic structure. Being an aldehyde, it is essential to note the following points:

  • Polarity: The presence of the carbonyl group (C=O) contributes to moderate polarity, suggesting that 4-phenylbutanal is likely to have solubility in polar solvents such as water to some extent. However, due to the hydrophobic phenyl group, complete solubility may not be achieved.
  • Solvent Compatibility: It is expected to be more soluble in organic solvents like alcohols, ethers, or other non-polar solvents due to its larger nonpolar character from the phenyl ring.
  • Temperature Effects: Temperature can greatly affect solubility; as temperature increases, solubility in various solvents could enhance due to increased molecular motion.

In conclusion, while 4-phenylbutanal exhibits a degree of solubility in polar solvents, its overall solubility profile is influenced by its molecular structure and the types of solvents used. "Like dissolves like," so it will perform better in organic mediums than in water.

Interesting facts

Facts about 4-Phenylbutanal

4-Phenylbutanal is an intriguing compound that falls within the category of aldehydes. It boasts a unique molecular structure and exhibits various properties that make it a subject of interest in the field of organic chemistry.

Chemical Structure and Characteristics

  • Functional Group: This compound features an aldehyde functional group, which is key in many chemical reactions, particularly in organic synthesis.
  • Substituents: The presence of a phenyl group enhances its aromatic characteristics and can influence its reactivity and interactions with other compounds.
  • Steric Influence: The relative position of the phenyl group can introduce steric effects, which can be critical in determining the outcome of certain reactions.

Applications in Industry and Research

  • Aromatic Compounds: With its distinctive aromatic features, 4-phenylbutanal can serve as a building block in the synthesis of other organic compounds.
  • Fragrance and Flavor Industry: Aldehydes, like 4-phenylbutanal, are often utilized in perfumes and flavorings due to their pleasant scents.
  • Biological Research: Studies have indicated potential biological activities of this compound, making it a candidate for research in medicinal chemistry.

In summary, 4-phenylbutanal's unique characteristics and functionality make it a valuable compound in both academic and industrial contexts. Its capability of participating in various chemical reactions opens up avenues for innovative discoveries and applications.

Synonyms
4-Phenylbutanal
18328-11-5
Benzenebutanal
4-Phenylbutyraldehyde
Butyraldehyde, 4-phenyl-
.gamma.-Phenylbutyraldehyde
DTXSID80171404
gamma-Phenylbutyraldehyde
DTXCID0093895
686-906-2
NHFRGTVSKOPUBK-UHFFFAOYSA-N
4-phenyl-butyraldehyde
MFCD00800383
phenylpropylketone
phenethylacetaldehyde
4-phenylbutyraldehye
4-phenyl-1-butanal
4-phenyl-butan-1-al
3-Benzyl propionaldehyde
SCHEMBL66826
SCHEMBL97266
SCHEMBL9312270
SCHEMBL10805807
SCHEMBL18171435
SCHEMBL27693771
SCHEMBL28000431
TAA32811
AKOS010079080
SB34596
AS-56525
SY236716
D71263
EN300-176881
Z993017616