Testosterone propionate | Solubility of Things

Identification

Molecular formula

C₂₂H₃₂O₃

CAS number

57-85-2

IUPAC name

[(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate

State

At room temperature, testosterone propionate is in a solid state, often found as a crystalline powder.

Melting point (Celsius)

118.00

Melting point (Kelvin)

391.15

Boiling point (Celsius)

489.70

Boiling point (Kelvin)

762.90

General information

Molecular weight

344.49g/mol

Molar mass

344.4880g/mol

Density

1.0800g/cm³

Appearence

Testosterone propionate is typically described as a white or off-white crystalline powder. Crystallinity is an important feature that can affect solubility and melting point. It's often odorless as well.

Comment on solubility

Solubility of [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate

The solubility of complex organic compounds like [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate can be influenced by various factors:

Molecular Structure: The intricate structure of this compound suggests a likelihood of unique solubility characteristics due to the presence of functional groups such as the propanoyloxy moiety, which can facilitate interactions with solvents.
Hydrophobic vs. Hydrophilic: With a predominantly hydrophobic tetradecahydro structure, this compound may exhibit limited solubility in water. However, it may dissolve better in organic solvents.
Intermolecular Forces: The solubility also depends on the nature of intermolecular forces at play between the compound and the solvent, including hydrogen bonding and van der Waals interactions.
Temperature and Pressure: Like many organic compounds, solubility tends to increase with temperature and can be affected by pressure conditions, particularly in non-aqueous media.

In summary, predicting the solubility of [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate requires a keen understanding of its molecular characteristics and the properties of potential solvents. Experimentation is often the key to unraveling the solubility profile of such complex compounds.

Interesting facts

Interesting Facts about [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopentaphenanthren-3-yl] propanoate

This compound, a complex derivative of the steroid family, presents fascinating aspects worth exploring. Its structure boasts of multiple stereocenters, specifically at the 3 and 17 positions, leading to unique stereochemistry that can influence its biological activity.

Key Features:

Biological Relevance: This compound may have implications in drug development, particularly due to its relation to steroid-like compounds.
Synthesis Potential: The intricate structure poses challenges and opportunities for organic synthesis; chemists continue to refine methods to construct such complex frameworks.
Pharmacological Properties: As a derivative of steroid compounds, it may exhibit hormonal activity, opening pathways for therapeutic applications in areas such as endocrinology and oncology.

Research indicates that compounds like this often interact with cellular receptors, thereby influencing various biological pathways. As emphasized by many chemists, understanding the nuances in structure can unlock significant breakthroughs in medicinal chemistry.

In summary, the study of [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta phenanthren-3-yl] propanoate not only enhances our comprehension of complex organic molecules but also emphasizes the intricacies involved in drug design and development. The journey through its synthesis and potential applications certainly keeps chemists intrigued!

Synonyms

Bolandiol dipropionate

DTXSID0057677

[(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate