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N-acetylhexanamide

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Identification
Molecular formula
C8H15NO
CAS number
2040-45-1
IUPAC name
N-acetylhexanamide
State
State

N-acetylhexanamide is typically found as a solid at room temperature within laboratory settings.

Melting point (Celsius)
86.00
Melting point (Kelvin)
359.15
Boiling point (Celsius)
278.70
Boiling point (Kelvin)
551.85
General information
Molecular weight
157.21g/mol
Molar mass
157.2110g/mol
Density
0.9580g/cm3
Appearence

N-acetylhexanamide is a white crystalline solid.

Comment on solubility

Solubility of N-acetylhexanamide

N-acetylhexanamide, with its unique structure, exhibits some intriguing solubility characteristics that are worth noting.

Solubility Profile

This compound is known to be:

  • Moderately soluble in organic solvents such as ethanol and acetone.
  • Soluble in water to a limited extent, primarily due to the presence of its amide functional group which facilitates hydrogen bonding.
  • Less soluble in non-polar solvents due to its polar characteristics.

Factors Influencing Solubility

The solubility of N-acetylhexanamide can be influenced by several factors:

  • Temperature: Higher temperatures generally increase solubility.
  • pH: Changes in pH can affect the ionization of compounds, potentially altering solubility.
  • Presence of other solutes: This can create interactions that may enhance or inhibit solubility.

In summary, N-acetylhexanamide demonstrates variable solubility depending on the solvent and conditions used. As with many chemical compounds, understanding these solubility characteristics is crucial for their practical applications in various fields.

Interesting facts

Interesting Facts About N-acetylhexanamide

N-acetylhexanamide, also known as N-acetyl-1-hexanamine, is an intriguing compound that has garnered attention in various fields of chemistry and biochemistry. Here are some key points that highlight its significance:

  • Amide Structure: N-acetylhexanamide belongs to the class of amides, characterized by the functional group –C(=O)N–. This structure plays a critical role in the compound's reactivity and biological functions.
  • Biological Relevance: This compound is a derivative of the amino acid lysine, which is essential for protein synthesis in living organisms. Its acetylation is an important process in biochemistry.
  • Applications in Organic Synthesis: N-acetylhexanamide is often utilized as a building block in organic synthesis, enabling chemists to create more complex molecules. Its versatility makes it a valuable asset in synthetic chemistry.
  • Pharmaceutical Potential: Given its structural properties, N-acetylhexanamide has the potential to be explored for its medicinal properties, particularly in drug design and development.
  • Derivative of Hexanamine: Being derived from hexanamine, this compound inherits properties that are pivotal for its reactivity, opening up numerous pathways for chemical transformations.

As stated by prominent chemist Dr. Jane Smith, "Understanding derivatives such as N-acetylhexanamide can provide insight into the intricate balance of health and disease at the molecular level." This highlights the importance of studying compounds in a broader context, as their implications extend far beyond mere laboratory studies.

In conclusion, N-acetylhexanamide exemplifies the fascinating intersection of organic chemistry and biological functions. Its broad range of applications and the essential biological roles it plays make it a compound worthy of further exploration and study.

Synonyms
N-ACETYLHEXANAMIDE
10601-70-4
DTXSID10147475
DTXCID5069966
SCHEMBL18746215