Skip to main content

Pent-2-enal

ADVERTISEMENT
Identification
Molecular formula
C5H8O
CAS number
1576-87-0
IUPAC name
pent-2-enal
State
State

At room temperature, pent-2-enal is in a liquid state. It is volatile and can readily become vapour at elevated temperatures due to its relatively low boiling point.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
119.00
Boiling point (Kelvin)
392.15
General information
Molecular weight
84.12g/mol
Molar mass
84.1200g/mol
Density
0.8474g/cm3
Appearence

Pent-2-enal is a colorless liquid that has a distinct, pungent odor. It is an unsaturated aldehyde that can be found in certain natural flavors and fragrances. Its appearance is typical of many simple aldehydes, appearing as a clear, transparent liquid at room temperature.

Comment on solubility

Solubility of Pent-2-enal

Pent-2-enal, also known as 2-pentenal, is an organic compound belonging to the aldehyde group. When considering its solubility, several key factors come into play:

  • Polarity: As an aldehyde, pent-2-enal possesses a polar carbonyl group, which enhances its solubility in polar solvents like water.
  • Hydrophobic Regions: The presence of the alkene (C=C) portion and the longer hydrocarbon chain introduces hydrophobic characteristics, making its solubility in water temperature-dependent.
  • solubility Potential: At lower concentrations, pent-2-enal is generally considered soluble in water. However, it is more **soluble** in organic solvents such as ethanol or ether.

It's worth noting that the solubility behavior can vary based on temperature and concentration. In summary:

  • In Water: Moderately soluble, depending on conditions.
  • In Organic Solvents: Highly soluble.

Understanding these solubility characteristics aids in predicting pent-2-enal's behavior in various chemical reactions and applications.

Interesting facts

Interesting Facts about Pent-2-enal

Pent-2-enal, an intriguing aldehyde with a five-carbon chain, is often studied for its unique structural and chemical properties. Here are some fascinating attributes that make it noteworthy:

  • Structure and Isomerism: Pent-2-enal features a double bond between the second and third carbon atoms, which gives it a distinct geometric configuration. The double bond allows for cis-trans isomerism, adding complexity to its reactivity and interactions.
  • Reactivity: As an aldehyde, pent-2-enal exhibits typical reactivity patterns, including susceptibility to nucleophilic attacks. Its dual functional groups (alkene and aldehyde) create opportunities for interesting reaction pathways, such as Michael additions and aldol condensations.
  • Applications in Synthesis: This compound is valuable in organic synthesis and serves as a building block for pharmaceuticals and other fine chemicals. The presence of both the alkene and aldehyde groups makes it a relevant precursor in synthetic pathways, offering routes to create more complex molecules.
  • Role in Flavor and Fragrance: Pent-2-enal is also noted for contributing to the aroma of certain foods. Its pleasant, slightly fruity scent can be utilized in the flavoring and fragrance industries, making it an aromatic compound of interest.

In Summary

Pent-2-enal stands out not just for its chemical structure but also for its diverse applications and reactivity. Understanding compounds like pent-2-enal can enhance our appreciation of organic chemistry and its role in both natural and synthetic systems.

Synonyms
2-PENTENAL
pent-2-enal
764-39-6
Propylidenacetaldehyd
beta-Aethyl-acrolein
3-ethylprop-2-enal
CHEBI:61722
alpha-pentenal
n-pentenal
Epitope ID:143636
DTXSID9061091
SB85393
DB-043361
NS00022763