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Solamargine

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Identification
Molecular formula
C45H73NO15
CAS number
20311-51-7
IUPAC name
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate
State
State
Solamargine is typically found as a solid at room temperature. It is often handled in crystalline or powdered form for research and industrial applications.
Melting point (Celsius)
285.00
Melting point (Kelvin)
558.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
868.08g/mol
Molar mass
868.0800g/mol
Density
1.3320g/cm3
Appearence

Solamargine is a glycoalkaloid that appears as a crystalline solid. It is found in various plants in the Solanum genus, often appearing as a white to off-white powder.

Comment on solubility

Solubility of [7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate

The solubility of the compound [7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate can be influenced by several factors, especially its molecular structure. Here are some key points to consider:

  • Polarity: The presence of multiple hydroxyl groups in the structure increases the compound's polarity, which generally enhances solubility in polar solvents, including water.
  • Hydrogen bonding: The ability to form hydrogen bonds due to the hydroxyl groups likely contributes to better solubility in aqueous solutions.
  • Hydrophobic regions: Some non-polar parts of the molecule can lead to decreased solubility in water, potentially making it more soluble in organic solvents such as ethanol or methanol.
  • Temperature: As with many compounds, increasing temperature can enhance solubility, making it useful in varied applications.

In summary, the solubility behavior of this compound is a balance of its polar and non-polar portions, which can be summarized as:

  1. **Increased solubility** in polar solvents due to **hydrogen bonding** capabilities.
  2. **Reduced solubility** in non-polar solvents due to hydrophobic characteristics.
  3. **Temperature dependency** may also play a role in enhancing its solubility profile.

Overall, understanding the solubility of this compound is essential for its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about [7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate

This complex compound, known for its intricate molecular structure, showcases the fascinating interplay of organic chemistry and biological significance. Here are some compelling aspects of this compound:

  • Biological Applications: Compounds like this one often exhibit biological activity that can be harnessed for medicinal purposes, including anti-inflammatory and antioxidant properties.
  • Structural Complexity: The combination of a pyrrolizine ring with multiple functional groups makes this compound a compelling subject for synthetic chemists, who strive to create similar compounds through innovative synthetic methods.
  • Synthetic Routes: Understanding how to synthesize such compounds opens doors to the development of new drugs or agrochemicals, driving research in both pharmaceutical and agricultural sectors.
  • Potential Natural Sources: Similar structures may be found in naturally occurring compounds, leading to interesting inquiries about the ecological roles they play in plants or other organisms.
  • Systems Biology Perspective: Studying such complex molecules encourages a more integrated systems approach, where their interactions within biological systems can be explored, enhancing our understanding of metabolic pathways.

In summary, the exploration of [7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate not only showcases the beauty of molecular architecture but also opens new avenues for research and discovery in various scientific fields.

Synonyms
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate
[7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate
XH180148