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Testosterone acetate

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Identification
Molecular formula
C23H34O3
CAS number
1045-69-8
IUPAC name
(17-acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate
State
State
At room temperature, testosterone acetate is a solid, typically found in a powdered form.
Melting point (Celsius)
140.00
Melting point (Kelvin)
413.20
Boiling point (Celsius)
446.70
Boiling point (Kelvin)
719.90
General information
Molecular weight
384.55g/mol
Molar mass
384.5490g/mol
Density
1.0800g/cm3
Appearence

Testosterone acetate is a white crystalline powder that is odorless. This compound is often used in the development of pharmaceuticals due to its role as an androgen steroid hormone.

Comment on solubility

Solubility of 17-acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl acetate

The solubility of the compound (17-acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate can be quite fascinating, as it demonstrates several key characteristics:

  • Polarity: This compound, with its multiple methyl groups and acetate function, suggests that it has both polar and nonpolar regions. The acetate group contributes to some polar characteristics, which may enhance solubility in polar solvents.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents like ether or chloroform, rather than in water due to its hydrophobic hydrocarbon backbone.
  • Temperature Effects: As with many organic compounds, solubility could increase with temperature. Thus, heating the solvent might facilitate dissolution.

To emphasize its nature, one could say, "Understanding solubility isn't merely about whether a compound dissolves; it's about how its molecular structure interacts with different environments." The interplay between its various structural components shapes its solubility profile intriguingly.

In summary, the solubility dynamics of this compound will depend heavily on environmental factors such as temperature and solvent choice, making it a compelling subject for further study in organic chemistry.

Interesting facts

Interesting Facts about 17-Acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl Acetate

This compound, often associated with complex organic chemistry, exhibits fascinating properties and potential applications. Here are some intriguing aspects:

  • Origin: The compound belongs to a class of steroids, which are organic compounds characterized by a core structure of four fused carbon rings. This structural complexity is what gives rise to its diverse chemical behaviors.
  • Biological Relevance: Compounds like this one can be seen as precursors or analogs in the development of pharmaceuticals, particularly in hormone-related research.
  • Synthesis: The synthesis of this compound often involves intricate multi-step organic reactions. Understanding these reactions can enhance one’s knowledge of synthetic organic chemistry and steroid biology.
  • Potential Applications: Due to its acetyl functional group, it may exhibit properties useful in medicinal chemistry. Acetylation is a common modification that can alter a molecule's pharmacokinetics and biological activity.

Research and Study

Researchers are continually exploring the properties of similar compounds through:

  • Analytical Techniques: Utilizing methods such as NMR (Nuclear Magnetic Resonance) and mass spectrometry to analyze the structure and confirm the identities of complex molecules.
  • Biological Assays: Assessing the compound's interactions within biological systems, which can illuminate its pharmacological potential.

In conclusion, 17-acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl acetate is not just a compound but a gateway into the compelling world of organic chemistry and steroid research. As always, further research holds the promise of uncovering more about its mechanisms and applications.

Synonyms
NSC73880
17-Hydroxy-6.alpha.-methylpregn-4-en-20-one acetate
NCIOpen2_008936
CHEMBL4762115
Pregn-4-en-20-one, 17-hydroxy-6.alpha.-methyl-, acetate
Pregn-4-en-20-one, 17-(acetyloxy)-6-methyl-, (6.alpha.)-
(17-acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate
6-Methyl-20-oxopregn-4-en-17-yl acetate