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Testosterone acetate

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Identification
Molecular formula
C21H30O3
CAS number
1045-69-8
IUPAC name
(13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl) acetate
State
State

At room temperature, testosterone acetate is a solid. It is commonly processed and stored in its crystalline powder form, making it relatively easy to handle and measure for various applications.

Melting point (Celsius)
139.00
Melting point (Kelvin)
412.15
Boiling point (Celsius)
515.00
Boiling point (Kelvin)
788.15
General information
Molecular weight
330.47g/mol
Molar mass
330.4650g/mol
Density
1.1456g/cm3
Appearence

Testosterone acetate typically appears as a white to off-white crystalline powder. It is relatively odorless and stable under standard conditions. Its powdered form makes it suitable for use in various pharmaceutical formulations.

Comment on solubility

Solubility of (13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl) acetate

The solubility of (13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl) acetate can be influenced by a variety of factors, including its chemical structure and polarity.

Here are some key points to consider regarding its solubility:

  • Polarity: The presence of functional groups such as the acetate moiety suggests that the compound may exhibit some degree of polarity, which could affect its solubility in polar solvents like water.
  • Solvent Interaction: Generally, non-polar compounds are more soluble in non-polar solvents, whereas polar compounds tend to dissolve better in polar solvents.
  • Temperature Effects: Increased temperatures generally enhance the solubility of solid compounds in liquids, allowing for better dissolution.
  • Concentration of Solvent: In concentrated solutions, solute-solute interactions may inhibit solubility, making it essential to consider solvent concentration.

In conclusion, while specific quantitative solubility data for (13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl) acetate may not be readily available, understanding the role of structure, polarity, and environmental factors can provide valuable insights into its solubility behavior.

Interesting facts

Interesting Facts about 13-Methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl Acetate

The compound 13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl acetate holds significance in the realm of organic chemistry, primarily due to its unique structure and biological relevance. Here are some engaging insights about this compound:

  • Chemical Structure: The complex structure of this compound features a cyclopenta[a]phenanthrene core, which is a fused polycyclic system. This configuration contributes to its unique chemical properties and reactivity.
  • Biological Activity: Compounds that are derived from similar structures often display interesting biological activities. Research into related compounds suggests that they may exhibit effects on hormonal balance and could have implications in herbal medicine.
  • Synthetic Pathways: The synthesis of such complex structures often involves multiple steps and careful consideration of stereochemistry. Chemists engage in crafting reactions that not only build the desired compound but also minimize by-products.
  • Potential Applications: The acetate functional group in this compound opens paths for esterification reactions, which can be exploited in medicinal chemistry for drug development.
  • Environmental Considerations: As with many organic compounds, understanding the metabolic pathways and degradation of such complex molecules in the environment is crucial for assessing their ecological impact.

In summary, 13-methyl-3,17-dioxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-10-yl acetate serves as a noteworthy example of the intricate world of organic compounds. Its unique structure and potential applications make it an interesting subject for further study in both academic and practical settings.

Synonyms
4147-12-0
10-Hydroxyestra-1,4-diene-3,17-dione acetate
3,17-dioxoestra-1,4-dien-10-yl acetate
DTXSID50961738