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Testosterone propionate

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Identification
Molecular formula
C22H32O3
CAS number
57-85-2
IUPAC name
(13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) propanoate
State
State

At room temperature, testosterone propionate is typically a solid. It is stable under ordinary conditions but should be kept in a dry environment to prevent degradation.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
394.15
Boiling point (Kelvin)
667.30
General information
Molecular weight
344.49g/mol
Molar mass
344.4880g/mol
Density
1.1455g/cm3
Appearence

Testosterone propionate appears as a white or creamy white crystalline powder. It is characterized by its lack of significant odor, but may have a slight ester-like scent upon close inspection.

Comment on solubility

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

The solubility of the compound C22H32O3 can be influenced by various factors, including its molecular structure and interactions with solvents. Here are some key points regarding its solubility:

  • Polarity: The presence of functional groups, such as the propanoyloxy moiety, suggests that the compound may exhibit polar characteristics, which can enhance its solubility in polar solvents like water.
  • Saturated Structure: The saturated nature of the compound indicates that it may have limited solubility in non-polar solvents, though saturated hydrocarbons typically have low solubility in water.
  • Hydrophobic Interactions: The bulky decahydrocyclopenta[a]phenanthren structure contributes to hydrophobic character, likely resulting in a preference for organic solvents over aqueous environments.
  • Temperature Effects: As with many organic compounds, increased temperatures can enhance solubility, so heating may positively affect its dissolution properties in suitable solvents.

Summarily, while C22H32O3 may dissolve in polar solvents due to its functional groups, its hydrophobic features and bulky structure suggest limited solubility in water, supporting a preference for non-polar organic solvents. Therefore, when considering solvent choices, it is crucial to balance polarity and molecular structure for optimal solubility results.

Interesting facts

Interesting Facts about (13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta [a] phenanthren-17-yl) propanoate

This compound, known for its complex structure and intriguing characteristics, offers a fascinating glimpse into the world of organic chemistry. Here are some enlightening insights about it:

  • Structural Complexity: The compound features a multi-ring structure, typical of many steroids and complex organic molecules. Its decahydrocyclopenta[a]phenanthrene framework adds to its unique properties and behavior in various chemical environments.
  • Functional Groups: The presence of a propanoyloxy group suggests the potential for interesting reactivity. This functional group can undergo reactions such as esterification and hydrolysis, making it notable in synthetic organic chemistry.
  • Anticipated Applications: Compounds with similar structures are often studied for their biological activity. This could include anti-inflammatory, anabolic, or even anticancer properties, highlighting the importance of such compounds in medicinal chemistry.
  • Nature of Synthesis: The synthesis of such complex molecules often involves multiple steps. Techniques like ring closure reactions, asymmetric synthesis, and protective group strategies might be employed, providing students and chemists alike a valuable learning experience.
  • Historical Context: Compounds in this structural family have been synthesized and studied since the mid-20th century, with many leading to the development of various pharmaceuticals. Understanding their synthesis and properties can illuminate the evolution of modern medicinal compounds.

In summary, the intriguing (13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta [a] phenanthren-17-yl) propanoate not only exemplifies the beauty of organic synthesis but also potentially opens doors to future medicinal advancements.

Synonyms
17-BETA-ESTRADIOL3,17-DIPROPIONATE
Oprea1_555259
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, dipropanoate
CHEMBL4787734
DTXSID50859202
beta -Estradiol 3,17-dipropionate
STK366310
AKOS005443350
DS-017210
estra-1(10),2,4-triene-3,17-diyl dipropanoate
estra-1,3,5(10)-triene-3,17-diyl dipropanoate