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Myristicamide

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Identification
Molecular formula
C20H41NO2
CAS number
112-84-5
IUPAC name
N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide
State
State

At room temperature, Myristicamide is typically found in a solid state. It is often utilized in this form for various industrial and cosmetic applications.

Melting point (Celsius)
88.50
Melting point (Kelvin)
361.65
Boiling point (Celsius)
416.60
Boiling point (Kelvin)
689.75
General information
Molecular weight
285.48g/mol
Molar mass
285.4760g/mol
Density
0.9202g/cm3
Appearence

Myristicamide appears as a white, waxy solid. It is typically available in powder or flaky form and may exhibit a slight pearlescent luster.

Comment on solubility

Solubility of N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide

N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide (C20H41NO2) exhibits interesting solubility properties that are influenced by its unique structure.

  • Polarity: The presence of both hydroxyl (-OH) groups and the amide group enhances its polarity, which generally increases solubility in polar solvents.
  • Hydrophobic Characteristics: The long heptadecyl chain contributes significant hydrophobic character, which may limit solubility in highly polar solvents.
  • Solvent Compatibility: This compound is likely more soluble in alcohols, dimethyl sulfoxide (DMSO), and other organic solvents than in water, due to its hydrophobic tail.
  • Temperature Effects: Solubility can also vary with temperature; increased temperatures may dissolve the compound better in certain solvents.

In summary, while N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide can be anticipated to have moderate solubility properties, its specific solubility is greatly influenced by the solvent and environmental conditions. In practical applications, it is essential to consider these factors to ensure effective utilization of this compound.

Interesting facts

Interesting Facts About N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide

N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide, a fascinating compound in the realm of organic chemistry, is noteworthy for several reasons:

  • Amphiphilic Nature: This compound possesses both hydrophilic and hydrophobic properties, making it an important candidate for applications in surfactants and emulsifiers. This amphiphilic nature allows it to stabilize mixtures of oil and water.
  • Biochemical Significance: The presence of a hydroxyl group (-OH) contributes to its potential biological activity. Hydroxy compounds often play crucial roles in various biochemical pathways, including those involved in lipid metabolism.
  • Applications in Cosmetics: The compound's moisturizing properties can be beneficial in the cosmetic industry. It can serve as a key ingredient in formulations designed to enhance skin hydration and improve sensory feel.
  • Research and Development: Researchers are exploring its applications as a potential drug delivery agent, particularly in systems designed to release therapeutic agents in a controlled manner.
  • Green Chemistry: The synthesis and application of this compound align with principles of green chemistry, promoting the use of renewable resources and environmentally friendly processes.

As we study compounds like N-[2-hydroxy-1-(hydroxymethyl)heptadecyl]acetamide, we unveil their potentials and contributions to various fields. The journey from a simple chemical structure to its wide array of applications is a testament to the beauty and complexity of chemistry.

Synonyms
2-acetaminooctadecane-1,3-diol
Cer 18:0;2O/2:0
N-(1,3-dihydroxyoctadecan-2-yl)acetamide
SPC101210;SPC-101210;SPC 101210
SCHEMBL445999
CRJGESKKUOMBCT-UHFFFAOYSA-N