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Squalamine

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Identification
Molecular formula
C30H49NO
CAS number
142920-48-5
IUPAC name
N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine
State
State

Squalamine is typically in a solid state at room temperature.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
384.65g/mol
Molar mass
384.6480g/mol
Density
1.0123g/cm3
Appearence

Squalamine is an aminosterol that appears as a white to off-white powder. It is known for its crystallinity and the solid form typically consists of fine granules.

Comment on solubility

Solubility of N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine

The solubility of N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine can be described as complex due to its unique structure. Understanding the solubility characteristics of this compound involves considering various factors:

  • Polarity: The presence of multiple carbon chains and nitrogen suggests varying degrees of polarity. Polar solvents may not dissolve this compound effectively.
  • Hydrophobicity: Given the long hydrocarbon chains, the compound exhibits significant hydrophobic characteristics, indicating better solubility in non-polar organic solvents.
  • Functional Groups: The amine functional group can interact with polar solvents to a degree, albeit the overshadowing hydrophobic properties tend to limit solubility in water.

Therefore, it is likely that N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine will be:

  1. Insoluble or only slightly soluble in water.
  2. More soluble in organic solvents such as ethanol, methanol, or chloroform.

As a general principle, “like dissolves like” holds true, making the assessment of solubility a crucial aspect for applications involving this compound. Further experimental evaluations will provide insight into the solubility profile under varying conditions.

Interesting facts

N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine

N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine is a fascinating organic compound with notable applications in various fields, including biochemistry and materials science. As a member of the amine family, this compound offers several intriguing characteristics and uses:

  • Functionality: The presence of multiple methyl groups contributes to the compound's hydrophobicity, influencing its interactions and solubility properties. This hydrophobic nature can enhance its utility in formulating specialized materials.
  • Biological Relevance: The structure of this compound suggests potential applications in pharmaceutical chemistry. The triene system may allow the compound to exhibit biological activity akin to natural compounds found in living organisms.
  • Synthetic Versatility: The synthesis of N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine illustrates the creativity involved in organic synthesis, showcasing how chemists can manipulate fundamental building blocks to create complex structures.
  • Polymer Precursor: Due to its functional groups, this compound may serve as a precursor for creating polymers with tailored properties, which can be utilized in coatings, adhesives, and other industrial applications.

In the words of a renowned chemist, “The beauty of chemistry lies in its ability to transform simple molecules into complex systems.” This compound is a perfect example of how molecular transformations can lead to materials with unique characteristics.

Overall, N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine is not just a compound; it is a gateway to a myriad of scientific explorations and innovations, embodying the dynamic nature of chemical research.

Synonyms
SCHEMBL3951138