Skip to main content

Testosterone benzoate

ADVERTISEMENT
Identification
Molecular formula
C26H32O3
CAS number
5721-91-5
IUPAC name
(13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) benzoate
State
State
At room temperature, testosterone benzoate is a solid, typically appearing as a crystalline powder.
Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
189.10
Boiling point (Kelvin)
462.25
General information
Molecular weight
372.54g/mol
Molar mass
372.5400g/mol
Density
1.1300g/cm3
Appearence

Testosterone benzoate is typically a white to off-white crystalline powder. This compound is solid at room temperature and is often used in various steroid formulations.

Comment on solubility

Solubility of (13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) benzoate

The solubility profile of (13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) benzoate is quite intriguing and can be influenced by several factors:

  • Polarity: The compound's large hydrophobic regions, particularly the hydrocarbon chains and phenanthrene structure, may limit its solubility in polar solvents.
  • Solvent Interactions: It is likely to dissolve better in non-polar solvents, such as chloroform or hexane, due to its hydrophobic nature.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for enhanced solvation processes.

In practical terms, one might observe that:

  1. In water, the solubility is expected to be very low.
  2. In organic solvents such as ethyl acetate, the compound may exhibit moderate solubility.

Overall, the solubility of this compound can be described as limited in polar environments, with a more favorable solvation in non-polar solvents, making it essential to consider the solvent choice for any applications or further studies involving this compound.

Interesting facts

Interesting Facts about 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl benzoate

This compound, known for its complex structure, belongs to the class of steroid-like compounds, which are fascinating in both biological and medicinal chemistry. Here are some noteworthy points:

  • Natural Occurrence: Its structure is reminiscent of natural steroids, suggesting potential biological activities and roles in various organisms.
  • Biological Relevance: Compounds with similar structures have been studied for their hormonal activities, binding to steroid receptors, and influencing various biological pathways.
  • Synthetic Interest: Chemists are often interested in synthesizing such compounds for pharmaceutical purposes, as they can serve as intermediates in drug development.
  • Analytical Studies: The intricate architecture of this compound provides excellent opportunities for analytical methods and spectroscopy to unravel its properties and behavior.

As a student or researcher in chemistry, you might appreciate the challenges and creative approaches required to synthesize and study compounds like this:

  1. Challenging Synthesis: The multi-ring structure presents challenges in achieving high yields during synthesis, urging chemists to innovate.
  2. Functional Modifications: Modification of specific functional groups can lead to variations in biological activity and specificity.
  3. Research Opportunities: Its complexity invites further research into potential medical applications, including anti-inflammatory and anticancer activities.

In summary, the compound 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl benzoate not only exemplifies the beauty of organic chemistry through its fascinating structure but also represents the myriad possibilities for research and application in the scientific community.

Synonyms
SCHEMBL18467888
(13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) benzoate