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Testosterone acetate

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Identification
Molecular formula
C23H32O3
CAS number
1045-69-8
IUPAC name
(10R,13S,17S)-3-(cyclopentoxy)-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-ol
State
State

Solid at room temperature.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
431.60
Boiling point (Kelvin)
704.80
General information
Molecular weight
330.47g/mol
Molar mass
330.4660g/mol
Density
1.0450g/cm3
Appearence

White or off-white crystalline powder.

Comment on solubility

Solubility of (10R,13S,17S)-3-(cyclopentoxy)-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-ol

The solubility of the compound (10R,13S,17S)-3-(cyclopentoxy)-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-ol with the formula C23H32O3 reflects intriguing characteristics due to its complex structure. Understanding its solubility is essential for applications in pharmaceuticals and materials science. Here are key insights on its solubility:

  • Hydrophobicity: Given its extensive carbon framework, the compound is likely to exhibit significant hydrophobic properties, leading to limited solubility in polar solvents like water.
  • Solubility in Organic Solvents: Compounds with similar structures often show enhanced solvability in organic solvents such as ethanol, acetone, or other non-polar solvents.
  • Influence of Functional Groups: The presence of the hydroxyl group (-OH) may impart some degree of hydrophilicity, enabling better solubility in a few aqueous environments and possibly facilitating interactions with biological systems.
  • Temperature Effects: Solubility can be influenced by temperature variations; higher temperatures generally increase solubility in organic solvents.

In summary, the solubility behavior of C23H32O3 compound can be characterized as moderate to low in water, with more favorable interactions anticipated in organic solvents. Understanding these solubility trends is crucial for effectively utilizing this compound in various applications.

Interesting facts

Interesting Facts About (10R,13S,17S)-3-(Cyclopentoxy)-10,13,17-Trimethyl-1,2,7,8,9,11,12,14,15,16-Decahydrocyclopenta[a]phenanthren-17-ol

This intriguing compound showcases the intricate world of organic chemistry, specifically within the realm of steroid-like structures. Its complex molecular architecture is marked by several notable features:

  • Structural Isomerism: With multiple chiral centers, this compound exhibits a variety of stereoisomers, which can lead to different biological activities. Understanding its stereochemistry is crucial, especially in pharmacology.
  • Functional Groups: The presence of the cyclopentoxy group adds unique properties, potentially influencing both solubility and stability. This functionalization allows for a wide range of chemical reactivity.
  • Biological Relevance: Compounds with similar structures are often studied for their potential roles as hormones or hormone precursors. Their interactions in biological systems can reveal significant insights into metabolic processes.
  • Natural Sources: Many steroids and steroid-like compounds are derived from natural sources, such as plants and animals. Investigating the biosynthesis of this compound could open doors to understanding its ecological role.

As one delves deeper into its chemical profile, one can appreciate the balance between complexity and functionality that this compound embodies. Its intricate design not only exemplifies advanced synthetic chemistry but also poses exciting questions for future research in medicinal chemistry.

In the words of renowned chemist Robert H. Grubbs, "The beauty of chemistry lies not only in the results but also in the journey of discovery." This compound is a testament to that journey, encouraging scientists and students alike to explore and uncover its mysteries.