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N-Phenylhexanamide

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Identification
Molecular formula
C12H17NO
CAS number
1132-97-8
IUPAC name
N-phenylhexanamide
State
State

At room temperature, N-Phenylhexanamide is typically a solid, which can vary in form from crystalline to powder.

Melting point (Celsius)
66.00
Melting point (Kelvin)
339.15
Boiling point (Celsius)
353.00
Boiling point (Kelvin)
626.15
General information
Molecular weight
191.27g/mol
Molar mass
177.2600g/mol
Density
1.0104g/cm3
Appearence

N-Phenylhexanamide appears as a colorless to pale yellow solid. It may also be found as a crystalline powder, depending on its purity and manufacturing process. This compound is characterized by a distinct odor typical of amides.

Comment on solubility

Solubility of N-phenylhexanamide

N-phenylhexanamide, with a chemical formula of C13H17NO, exhibits distinct solubility characteristics influenced by its molecular structure. Its solubility can be summarized as follows:

  • Polar and Nonpolar Solvents: N-phenylhexanamide demonstrates solubility in organic solvents, primarily due to its nonpolar hydrocarbon chain.
  • Water Solubility: This compound is generally insoluble in water owing to its hydrophobic characteristics, which limit water interactions.
  • Temperature Variability: The solubility may increase with elevated temperatures, allowing for greater compatibility in organic mixtures.
  • Influence of pH: The solubility can be affected by the pH of the surrounding medium, as ionization of the amide group may facilitate dissolution in certain conditions.

In groupings of solutes, it can generally be stated that like dissolves with like; thus, N-phenylhexanamide is best paired with other nonpolar or slightly polar solvents. As noted, its limited water solubility is a critical factor in various applications, especially in settings requiring solubility considerations.

Interesting facts

Interesting Facts about N-phenylhexanamide

N-phenylhexanamide is an intriguing compound that belongs to the class of amides, which are derivatives of carboxylic acids. Here are some captivating insights about this chemical:

  • Structure and Properties: N-phenylhexanamide features a hexanamide backbone combined with a phenyl group, resulting in unique chemical properties that make it a valuable substance in various applications.
  • Applications: This compound is widely explored for its potential in pharmaceutical research. Its structure can serve as a scaffold for designing new drugs, especially within the realm of anti-inflammatory and analgesic agents.
  • Biological Activity: Research indicates that N-phenylhexanamide and its derivatives exhibit interesting biological activities, which can lead to the development of novel therapeutic compounds. The phenyl ring can enhance the interaction with biological targets.
  • Synthesis: The synthesis of N-phenylhexanamide can involve the reaction of hexanoic acid with an amine or aromatic compound, representing typical amide formation techniques. This reaction pathway is significant for students in organic chemistry to understand.
  • Research Potential: Studies on N-phenylhexanamide continue to unveil its potential in various fields, including materials science and biochemistry. Scientists are particularly interested in its capacity to form stable complexes with metal ions.

In conclusion, N-phenylhexanamide is more than just a compound; it acts as a bridge between organic chemistry and medicinal applications. Its unique properties and potential future uses keep it a focal point for ongoing research and discovery.

Synonyms
Hexanilide
N-Phenylhexanamide
N-Phenylcaproamide
Hexanamide, N-phenyl-
Caproic acid anilide
HEXANANILIDE
N-(n-Hexanoyl)aniline
UNII-9SBU2U1Q5Y
NSC 1498
9SBU2U1Q5Y
BRN 2414417
AI3-01347
NSC-1498
DTXSID50211144
4-12-00-00392 (Beilstein Handbook Reference)
Hexanamide, N-phenyl-(9CI)
DTXCID50133635
jbtchcwunmzneo-uhfffaoysa-n
621-15-8
CHEMBL4754649
Hexanamide, N-phenyl- (9CI)
4-butylacetanilide
NSC1498
4-n-butylacetanilide
4-n-butyl-acetanilide
WLN: 5VMR
SCHEMBL1897242
BDBM50554337
AKOS003867206
Q27273043