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Testosterone propionate

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Identification
Molecular formula
C22H32O3
CAS number
57-85-2
IUPAC name
[(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] propanoate
State
State

At room temperature, testosterone propionate is typically found as a solid, specifically in a crystalline powder form. It is insoluble in water but soluble in organic solvents like alcohol and benzene.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
399.15
Boiling point (Kelvin)
672.15
General information
Molecular weight
344.49g/mol
Molar mass
344.4880g/mol
Density
1.0800g/cm3
Appearence

Testosterone propionate is a white or creamy white crystalline powder. It is odorless and has a bitter taste. The powder is stable under normal conditions and is usually supplied in sealed packaging to avoid degradation.

Comment on solubility

Solubility of [(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] propanoate

The solubility of complex organic compounds like [(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] propanoate can often be influenced by various factors. Understanding its solubility characteristics is crucial for applications in pharmaceuticals, cosmetics, and material sciences. Here's a detailed exploration of its solubility attributes:

  • Solvent Effects: The solubility of this compound is likely to vary significantly in different solvents. Polar solvents (e.g., water) may not dissolve it well due to its hydrophobic nature, whereas non-polar organic solvents (like hexane or chloroform) may enhance solubility.
  • Temperature Influence: Generally, solubility increases with temperature in most solids. This means that heating the solvent may improve the dissolution of the compound, leading to a more saturated solution.
  • pH Considerations: As this compound does not bear acidic or basic functional groups, its solubility may remain largely stable across a range of pH levels, although interactions with other compounds in solution can cause variations.
  • Concentration Dynamics: In concentrated solutions, solubility may exhibit changes due to potential precipitation of the compound or formation of aggregates, depending on the nature of the solvent and other solutes present.

Overall, the solubility of [(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] propanoate is a multifaceted aspect that requires careful consideration of the above factors to optimize its usage in various fields.

Interesting facts

Interesting Facts about (5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl propanoate

This compound, while perhaps not commonly known, plays an intriguing role in the chemical and pharmaceutical domains. Here are some fascinating aspects to consider:

  • Steroid Structure: The intricate structure of this compound suggests it might belong to a class of compounds associated with steroidal frameworks. Its multi-ring system is analogous to many biologically active steroids.
  • Biological Relevance: Given its steroid-like properties, it could potentially exhibit biological activities, making it a candidate for further investigation in medicinal chemistry.
  • Synthesis: The synthetic routes to such complex molecules often involve intricate organic transformations, showcasing the creativity and precision of chemists in their design and execution of synthetic pathways.
  • Chirality: The presence of multiple chiral centers adds a layer of complexity to this compound, as chirality can significantly influence its biological activity and pharmacokinetics.
  • Potential Applications: Depending on its specific biological activities, this compound might find applications in areas such as:
    • Hormonal therapies
    • Anti-inflammatory drugs
    • Regenerative medicine

The emphasis on understanding the specific interactions this compound has within biological systems can open up new avenues for research. As we delve further into the exploration of such complex molecules, we gain not only insight into their potential therapeutic uses but also an appreciation for the art and science of organic chemistry.

As the adage goes, "Chemistry is the art of understanding matter and its transformations." This compound exemplifies that principle, embodying a complex interplay of structure and function in the realm of chemical research.

Synonyms
Dihydrotestosterone propionate
Androstanolone propionate
855-22-1
stanolone propionate
EINECS 212-722-5
5-alpha-Dihydrotestosterone propionate
Dihydrotestosterone 17-beta-propionate
BRN 2628403
F06YUT08U8
UNII-F06YUT08U8
(5-alpha,17-beta)-17-(1-Oxopropoxy)androstan-3-one
Androstan-3-one, 17-(1-oxopropoxy)-, (5.alpha.,17.beta.)-
3-08-00-00576 (Beilstein Handbook Reference)
[(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] propanoate
5-.alpha.-Dihydrotestosterone propionate
5-alpha-ANDROSTAN-3-ONE, 17-beta-HYDROXY-, PROPIONATE
Androstan-3-one, 17-(1-oxopropoxy)-, (5-alpha,17-beta)-
Dihydrotestosterone 17-.beta.-propionate
5.ALPHA.-DIHYDROTESTOSTERONE PROPIONATE
DIHYDROTESTOSTERONE 17.BETA.-PROPIONATE
5.ALPHA.-ANDROSTAN-17.BETA.-OL-3-ONE PROPIONATE
5-.alpha.-Androstan-3-one, 17-.beta.-hydroxy-, propionate
((5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta(a)phenanthren-17-yl) propanoate
5alpha-dihydrotestosterone propionate
DIHYDROTESTOSTERONE 17BETA-PROPIONATE
5ALPHA-ANDROSTAN-17BETA-OL-3-ONE PROPIONATE
Androstan-3-one, 17-(1-oxopropoxy)-, (5-alpha,17-beta)-(9CI)
ANDROSTAN-3-ONE, 17-(1-OXOPROPOXY)-, (5ALPHA,17BETA)-
212-722-5
DHTP
17beta-Hydroxy-5alpha-androstan-3-one propionate
SCHEMBL1316924
XTAARPJDFFXHGH-GRPBBMKTSA-N
DTXSID801006059
NS00042931
17.beta.-Propanoyloxy-5.alpha.-androstan-3-one
(5alpha,17beta)-17-(1-Oxopropoxy)androstan-3-one
Q27277466