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Ceramide E

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Identification
Molecular formula
C33H65NO3
CAS number
100403-19-8
IUPAC name
N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide
State
State

At room temperature, Ceramide E is typically found in a solid state, presenting as either a waxy solid or flake depending on its exact formulation and purity level.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.10
Boiling point (Celsius)
555.20
Boiling point (Kelvin)
828.30
General information
Molecular weight
537.91g/mol
Molar mass
537.9870g/mol
Density
0.9873g/cm3
Appearence

Ceramide E is typically a white to off-white waxy solid that may appear in flake or powder form. Its appearance can also be described as creamy based on its application in various dermatological formulations.

Comment on solubility

Solubility of N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide

N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide, with the chemical formula C33H65NO3, demonstrates intriguing solubility characteristics influenced by its molecular structure.

Key solubility aspects include:

  • Polarity: The presence of hydroxyl (-OH) groups suggests that this compound may exhibit some level of polarity, allowing it to interact favorably with polar solvents such as water.
  • Hydrophobic Characteristics: Given the long hydrophobic alkyl chains, N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide is likely to be more soluble in non-polar organic solvents, such as hexane or chloroform.
  • Temperature Dependence: Its solubility may vary significantly with temperature changes, potentially increasing in non-polar solvents as temperature rises due to enhanced molecular motion.

Overall, while this compound may possess some water solubility due to its hydroxyl functionalities, its extensive hydrophobic sections imply a greater affinity for organic solvents, making it a versatile compound in diverse chemical applications.

Interesting facts

Interesting Facts about N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide

N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide, often referred to by its functional traits rather than its complex name, is an intriguing organic compound with various applications and properties.

Key Properties and Applications

  • Biological Relevance: This compound contains both amide and alcohol functional groups, making it a significant player in biological systems. It can participate in hydrogen bonding, influencing interactions in biological membranes.
  • Amphiphilic Nature: The presence of both hydrophilic (water-loving) and hydrophobic (water-repelling) regions allows this compound to act as a surfactant. This property is essential in applications such as drug delivery systems and formulation chemistry.
  • Synthetic Pathways: The synthesis of this compound often involves multi-step organic reactions starting from fatty acids or their derivatives. Understanding the synthetic route helps in tailoring its properties for specific applications.

Potential Uses

  • Cosmetic Industry: Due to its hydrophilic-hydrophobic balance, it may be utilized in personal care products for skin hydration and as an emulsifying agent.
  • Pharmaceutical Research: It has potential in drug design for modulating the pharmacokinetics of bioactive compounds, enhancing their therapeutic efficacy.
  • Surfactant Properties: Its unique structure permits it to lower the surface tension in solutions, leading to its role in cleaning products or as an agent that enhances solubility.

Moreover, there's fascinating structural diversity in compounds like this one, where minor changes in the molecular structure can lead to significant differences in functionality and behavior. As emphasized by chemists: "Small changes in molecular structure can lead to large changes in properties." This is a key reason why compounds like N-[2-hydroxy-1-(hydroxymethyl)heptadec-3-enyl]octanamide continue to be a focal point in research and product development.

In summary, this compound embodies the intersection of chemistry and practical application, highlighting the ongoing exploration and innovation within the field.

Synonyms
IN1378
74713-62-5
SCHEMBL2734735
Ceramide 8; D-erythro-N-Octanoylsphingosine; N-Octanoyl-C18-sphingosine
OCTANOIC ACID (2-HYDROXY-1-HYDROXYMETHYL-HEPTADEC-3-ENYL)-AMIDE
DTXSID70274372