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N-methylheptanamide

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Identification
Molecular formula
C8H17NO
CAS number
2044-53-5
IUPAC name
N-methylheptanamide
State
State
At room temperature, N-methylheptanamide is in a liquid state.
Melting point (Celsius)
-9.00
Melting point (Kelvin)
264.15
Boiling point (Celsius)
211.00
Boiling point (Kelvin)
484.15
General information
Molecular weight
143.24g/mol
Molar mass
143.2380g/mol
Density
0.8675g/cm3
Appearence
N-methylheptanamide appears as a colorless to yellow liquid. It has a characteristic amide odor.
Comment on solubility

Solubility of N-methylheptanamide

N-methylheptanamide, with the chemical formula C8H17NO, exhibits unique solubility properties that are significant in both industrial and laboratory settings. The solubility can be discussed through various aspects:

  • Polarity: N-methylheptanamide is an amide, which generally possesses polar characteristics due to the presence of the carbonyl group (C=O) and the nitrogen atom (N). This polarity affects how it interacts with solvents.
  • Aqueous Solubility: With its long hydrocarbon chain, N-methylheptanamide is likely to have low solubility in water. However, amides are typically more soluble in water than their corresponding hydrocarbons due to hydrogen bonding capabilities.
  • Solvent Compatibility: The compound shows better solubility in organic solvents such as diethyl ether, acetone, and chloroform due to its hydrophobic tail. In contrast, it may have limited interaction in polar solvents.
  • Temperature Effects: Solubility can change significantly with temperature; generally, increased temperature improves the solubility of organic compounds.

In summary, the solubility of N-methylheptanamide is influenced by its molecular structure and the nature of the solvent. As such, understanding these solubility dynamics is crucial for its effective application and utilization in various fields.

Interesting facts

Interesting Facts about N-methylheptanamide

N-methylheptanamide, an intriguing member of the amide family, holds a unique position in the study of organic compounds. Here are some interesting insights into this fascinating compound:

  • Structure and Composition: N-methylheptanamide is characterized by the presence of a methyl group attached to the nitrogen atom of the heptanamide. This structural modification enhances its chemical properties and reactivity.
  • Biological Importance: Compounds similar to N-methylheptanamide often play vital roles in biological systems, including acting as intermediates in metabolic pathways and serving as signaling molecules. Understanding such compounds can offer insights into biochemical mechanisms.
  • Uses in Synthesis: N-methylheptanamide can serve as a valuable building block in organic synthesis. Researchers often use it in the development of pharmaceuticals and agrochemicals, showcasing its role in advancing medicinal chemistry.
  • Environmental Significance: As with many organic amides, N-methylheptanamide can be analyzed for its environmental impact. Studying its degradation and interaction with various ecological systems is essential for assessing potential risks.
  • Research Opportunities: The compound presents several avenues for research, particularly in the fields of organic chemistry and materials science. Investigating its properties and reactions can lead to the discovery of novel applications and functionalities.

As a chemistry student or scientist, delving deeper into the world of N-methylheptanamide can enhance your understanding of organic compounds and their diverse roles in both nature and industry.
Exploring its synthesis, properties, and applications can spark curiosity and lead to exciting scientific discoveries.

Synonyms
HEPTANAMIDE, N-METHYL-
N-Methylenanthamide
N-Methylheptylamide
3400-24-6
N-methylheptanamide
NSC-76634
N-Methyloenanthsaureamid [German]
N-Methyloenanthsaureamid
NSC 76634
BRN 1747151
NSC76634
9PN2ZN4FKC
NCIOpen2_000926
SCHEMBL103896
DTXSID40187607
AKOS009163594