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Hexadecyl octadecyl propanetriol sulfomethyl ether

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Identification
Molecular formula
C40H80O10S
CAS number
/unknown
IUPAC name
[6-(2-hexadecanoyloxy-3-octadecanoyloxy-propoxy)-3,4,5-trihydroxy-tetrahydropyran-2-yl]methanesulfonic acid
State
State
This compound exists as a solid at room temperature. It remains stable under normal conditions of storage and use.
Melting point (Celsius)
72.00
Melting point (Kelvin)
345.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
793.37g/mol
Molar mass
793.3700g/mol
Density
1.2300g/cm3
Appearence

This compound is typically a white, waxy solid with a greasy texture. It is odorless and has a smooth consistency, making it suitable for personal care formulations like lotions and creams.

Comment on solubility

Solubility Insights

The compound [6-(2-hexadecanoyloxy-3-octadecanoyloxy-propoxy)-3,4,5-trihydroxy-tetrahydropyran-2-yl]methanesulfonic acid (C40H80O10S)

is characterized by its complex structure, which influences its solubility profile significantly. As a sulfonic acid derivative, it offers unique properties compared to non-sulfonated compounds.

Factors Influencing Solubility:

  • Hydrophilicity vs. Hydrophobicity: The presence of several hydrophobic aliphatic chains (hexadecanoyloxy and octadecanoyloxy) contributes to its overall lipophilic nature, while the methanesulfonic acid moiety introduces some degree of hydrophilicity.
  • Functional Groups: The trihydroxy groups enhance the potential for hydrogen bonding with polar solvents, which can increase solubility in specific environments.
  • Temperature and pH: Changes in temperature and pH can affect the ionization of the sulfonic acid group, potentially altering its solubility in aqueous solutions.

Such compounds typically demonstrate:

  1. Greater solubility in organic solvents, due to their hydrophobic characteristics.
  2. Limited solubility in water, depending on the balance of hydrophobic and hydrophilic elements in the molecule.
  3. Better solubility in polar organic solvents where they can better interact with solvent molecules.

In summary, the solubility of this compound is an intricate balance of its functional groups and hydrophobic regions, making it versatile yet challenging in various solvent systems. Understanding these solubility dynamics is essential for practical applications.

Interesting facts

Interesting Facts about [6-(2-hexadecanoyloxy-3-octadecanoyloxy-propoxy)-3,4,5-trihydroxy-tetrahydropyran-2-yl]methanesulfonic acid

This complex organic compound is a member of the class of molecules known as glycosides, which are notable for their wide range of applications in various fields including pharmaceuticals, biochemistry, and agriculture.

Key Features

  • Structural Complexity: This molecule features a unique tetrahydropyran ring fused with multiple hydroxy groups, contributing to its hydrophilicity and potential bioactivity.
  • Lipid Interaction: With the presence of hexadecanoyloxy and octadecanoyloxy groups, this compound demonstrates intriguing properties for lipid interaction, which can influence membrane dynamics.
  • Potential Applications: Due to its chemical structure, it may serve potential roles in drug delivery systems or as a surfactant, enhancing solubility and bioavailability of hydrophobic drugs.

Biological Significance

Compounds like this one are often investigated for their biological activities. The triol moiety indicates varied interaction possibilities with biological membranes, while the sulfonic acid group may impart certain functionalities such as increased solubility in aqueous environments.

Research Insights

Studies have identified that glycosides can have significant pharmacological effects such as anti-inflammatory and anti-cancer properties. The synthesis and modification of glycosides like this compound are critical for developing novel therapeutic agents.

In summary, examining the intricacies of [6-(2-hexadecanoyloxy-3-octadecanoyloxy-propoxy)-3,4,5-trihydroxy-tetrahydropyran-2-yl]methanesulfonic acid opens up a fascinating avenue for research and application in modern chemistry and pharmacology.

Synonyms
Sulfolipid 18:0
NSC650902
NSC-650902