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Mannitol Dipalmitate

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Identification
Molecular formula
C26H26O7
CAS number
21838-86-5
IUPAC name
(6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate
State
State

This compound is typically in a solid state at room temperature.

Melting point (Celsius)
138.00
Melting point (Kelvin)
411.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
458.49g/mol
Molar mass
458.4500g/mol
Density
1.3500g/cm3
Appearence

(6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate appears as a white crystalline powder.

Comment on solubility

Solubility of (6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate

(6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate is a complex organic compound characterized by its multi-functional hydroxyl groups and the presence of ester linkages. This structural intricacy plays a significant role in its solubility properties.

When considering the solubility of this compound, several factors are at play:

  • Polarity: The multiple hydroxyl (-OH) groups contribute to increased polarity, which can enhance solubility in polar solvents like water.
  • Hydrocarbon Chain: The hexyl portion introduces hydrophobic characteristics, potentially leading to decreased solubility in aqueous environments.
  • Hydrogen Bonding: The ability of hydroxyl groups to form hydrogen bonds can result in solubility in polar organic solvents, improving compatibility with compounds that exhibit similar properties.

In summary, the solubility of (6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate is likely to be:

  • High in polar solvents, owing to its hydroxyl groups.
  • Lower in non-polar solvents, due to its hydrophobic hexyl chain.

As with any organic compound, solubility can also be influenced by temperature and the presence of other solutes. Therefore, it's crucial to consider these variables during practical applications and testing.

Interesting facts

Interesting Facts about (6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate

(6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate is an intriguing compound known for its unique structure and applications in various fields. Below are some captivating aspects of this compound:

  • Complex Structure: This compound is characterized by a multi-hydroxy structure, integrating both aromatic and aliphatic elements. Its structure features multiple hydroxyl (-OH) groups, which contribute to its potential reactivity and interaction with biological systems.
  • Potential Applications: Compounds like (6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate may have various applications, particularly in the fields of pharmaceuticals and cosmetics. The phenolic component can exhibit antioxidant properties, potentially making it valuable as a protective agent in skincare formulations.
  • Role in Drug Delivery: Some research suggests that benzoate derivatives can enhance the solubility and absorption of active pharmaceutical ingredients. This raises interesting possibilities for developing more effective drug delivery systems.
  • Research Interest: Due to its unique combination of benzoate and hydroxy functionalities, this compound has attracted attention in academic research. Scientists explore its properties to gain insights into how similar compounds can be utilized in advanced materials or drug designs.
  • Biological Activity: The presence of hydroxyl groups may also influence the compound's biological activity, allowing it to interact with enzymes and other biomolecules. This can lead to investigations into its potential therapeutic effects.

Overall, (6-benzoyloxy-2,3,4,5-tetrahydroxy-hexyl) benzoate exemplifies the fascinating complexity of synthetic compounds in chemistry. Its structural diversity opens up numerous avenues for research and application, making it a subject of continued interest in the scientific community.

Synonyms
1,6-Dibenzoyl-D-mannitol
7226-27-9
(6-benzoyloxy-2,3,4,5-tetrahydroxyhexyl) benzoate
1,6-di-o-benzoyl-d-mannitol
NSC 113463
Glucitol, 1,6-dibenzoate, D-
NSC1693
1,6-Di-O-benzoylhexitol
Glucitol,6-dibenzoate, D-
1,6-Di-O-benzoylhexitol #
SCHEMBL23227764
DTXSID10993015
LDFVROHMRYBVGB-UHFFFAOYSA-N
NSC-1693
NSC113463
AKOS024325275
NSC-113463
SY365519