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Cholesterol

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Identification
Molecular formula
C27H46O
CAS number
57-88-5
IUPAC name
13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol
State
State
Cholesterol is a solid at room temperature, appearing as a waxy crystalline substance.
Melting point (Celsius)
147.00
Melting point (Kelvin)
420.00
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.00
General information
Molecular weight
386.65g/mol
Molar mass
386.6520g/mol
Density
1.0520g/cm3
Appearence
Cholesterol is a white, crystalline substance that is waxy in nature. It is typically odorless and tasteless.
Comment on solubility

Solubility of 13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol

The solubility of 13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol can be quite complex due to its unique structure. Here's a closer look at its solubility characteristics:

  • Polar vs. Nonpolar Solubility: This compound exhibits characteristics of a nonpolar molecule, making it more soluble in nonpolar solvents such as hexane and octane rather than in polar solvents like water.
  • Effects of Functional Groups: The presence of the hydroxyl (-OH) group enhances hydrogen bonding potential, potentially increasing solubility in alcohols and other polar aprotic solvents.
  • Temperature Influence: Solubility can often increase with temperature, so solubility tests should be conducted at various temperatures to gain comprehensive insights.
  • pH Sensitivity: Changes in pH can alter the ionization of the hydroxyl group, affecting solubility in different solvent systems.

In conclusion, while it can be *predicted* that 13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol is relatively insoluble in water, its behavior in various organic solvents displays intriguing dependency on molecular interactions and environmental conditions. Therefore, specific solubility testing is essential for practical applications.

Interesting facts

Interesting Facts about 13-Methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol

The compound 13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol, often referred to as a type of steroid due to its structural characteristics, exhibits fascinating properties that are worth exploring. Here are some noteworthy points about this intriguing molecule:

  • Biological Significance: Compounds like this are often studied for their potential roles in biological systems, particularly in relation to hormonal activity.
  • Structural Complexity: The extensive hydrocarbon framework paired with sulfur functional groups makes this compound a subject of interest in organic synthesis and medicinal chemistry.
  • Potential Applications: The research into similar compounds suggests potential uses in pharmaceuticals, where steroid-like structures are employed for therapies related to hormonal imbalances and other medical conditions.
  • Natural Occurrence: Similar steroids are found naturally in various organisms, hinting at a rich biosynthetic diversity and complex evolutionary pathways.
  • Research Opportunities: Ongoing studies aim to uncover more about the interactions this compound might have within living systems, offering opportunities for breakthroughs in drug development.

As a chemistry student or scientist, understanding the implications of such compounds can open avenues for research and innovative applications. The world of steroids and their derivatives continues to intrigue researchers, as these compounds often bridge the gap between synthetic chemistry and biological functionality.

In the words of a famous chemist, "Chemistry is the science of matter, and life is the highest form of matter." Studying compounds like this one exemplifies how closely tied chemistry is to understanding life itself.

Synonyms
17-alpha-Mercaptoestra-1,3,5(10)-trien-3-ol
10329-87-0
7438-72-4
NSC-524450
NSC524449
DTXSID60908311
NSC524450
NSC-524449
17-Sulfanylestra-1(10),2,4-trien-3-ol
Estra-1,5(10)-trien-3-ol, 17-mercapto-, 17-alpha-