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Testosterone Cypionate

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Identification
Molecular formula
C27H40O3
CAS number
58-20-8
IUPAC name
(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate
State
State
Testosterone Cypionate is a solid at room temperature, typically provided in powder form or as a solution in vials for injection.
Melting point (Celsius)
98.00
Melting point (Kelvin)
371.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
412.61g/mol
Molar mass
412.6050g/mol
Density
1.0080g/cm3
Appearence

Testosterone Cypionate appears as white or creamy-white crystalline powder that is odorless. It is stable under normal temperatures and pressures, and it has a characteristic crystalline appearance.

Comment on solubility

Solubility of (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate

The solubility of the compound with the formula C27H40O3 presents an intriguing challenge. This compound features a complex structure, which influences its interaction with solvents. Here are some key points regarding its solubility:

  • Solvent Polarity: The solubility is highly dependent on the polarity of the solvent used. Non-polar solvents might enhance the solubility of this compound due to its hydrophobic nature, while polar solvents could struggle to solubilize it effectively.
  • Temperature Effects: Increasing temperature tends to increase the solubility of most organic compounds. Thus, conducting experiments at elevated temperatures may yield better solubility results.
  • Structural Factors: The presence of large hydrocarbon chains and rings can contribute to a low solubility in water, limiting its aqueous solubility considerably.
  • Functional Groups: The ester functional group present could provide moderate solubility in organic solvents compared to hydrocarbons.

In sum, while the specific solubility data might not be widely available due to the complexity of the compound, one can infer that its solubility will be significantly influenced by the type of solvent, temperature, and structural characteristics that define its chemical behavior.

Interesting facts

Interesting Facts about (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate

This fascinating compound belongs to a category known as steroids, which play crucial roles in various biological functions, including hormone production and cellular processes. Here are some intriguing aspects to consider:

  • Chemical Structure: The compound features a complex structure with multiple rings and functional groups, indicating its potential for significant biological activity. The presence of a cyclopentyl group emphasizes its unique chemical behavior.
  • Biological Significance: Steroid compounds, like this one, are often considered for their therapeutic properties. They can influence a broad range of physiological activities in humans and other organisms.
  • Synthetic Applications: Due to its intricate structure, synthetic chemists may explore this compound in the development of new pharmaceuticals, particularly in the field of hormonal therapies.
  • Research Potential: The compound opens avenues for research in medicinal chemistry and biochemistry, with potential implications for understanding metabolic pathways and disease mechanisms.

In addition to its structural complexity, the study of (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate serves as an exceptional example of how even minor modifications in molecular design can lead to substantial shifts in biological activity and function.

Remember: Exploring the chemistry of such compounds not only enhances our understanding of biological systems but also paves the way for innovative developments in pharmaceuticals and biochemistry.

Synonyms
Depo-Testosterone cypionate
Testosterone 17.beta.-cypionate
NSC9157
3-Oxoandrost-4-en-17-yl 3-cyclopentylpropanoate
Testosterone 17.beta.-cyclopentylpropionate
(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate
SCHEMBL5021654
NS00015423