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Testosterone acetate

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Identification
Molecular formula
C23H32O3
CAS number
1045-69-8
IUPAC name
[(17R)-17-hydroxy-13-methyl-17-(2-methylallyl)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] acetate
State
State

At room temperature, testosterone acetate is in a solid state, being a crystalline powder.

Melting point (Celsius)
139.50
Melting point (Kelvin)
412.70
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
386.55g/mol
Molar mass
386.5510g/mol
Density
1.1000g/cm3
Appearence

Testosterone acetate is typically a white or off-white crystalline powder. It is not very soluble in water but can dissolve in organic solvents like ethanol and methanol.

Comment on solubility

Solubility of [(17R)-17-hydroxy-13-methyl-17-(2-methylallyl)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] acetate

The solubility of [(17R)-17-hydroxy-13-methyl-17-(2-methylallyl)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] acetate can be assessed through several key factors, including polarity, intermolecular interactions, and the nature of the solvent used.

Key Points on Solubility:

  • Polarity: The presence of functional groups in this compound indicates a level of polarity which may enhance solubility in polar solvents.
  • Solvent Choice: For effective solubilization, it is crucial to consider the solvent. This compound may show better solubility in organic solvents such as ethanol or dichloromethane.
  • Hydrophobic Interactions: Due to its bulky hydrocarbon structure, the compound may have limited solubility in water, reminiscent of other hydrophobic or lipophilic compounds.
  • Concentration Dependence: As with many organic compounds, solubility may vary significantly with concentration, potentially leading to saturation at higher levels.

In summary, understanding the solubility of [(17R)-17-hydroxy-13-methyl-17-(2-methylallyl)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] acetate requires an appreciation of its molecular characteristics and the interactions it can form with different solvents. As with many organic compounds, it is essential to test solubility empirically under various conditions to ascertain practical applications.

Interesting facts

Interesting Facts about [(17R)-17-hydroxy-13-methyl-17-(2-methylallyl)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] acetate

This complex compound, commonly recognized in the field of organic chemistry, is a derivative of a steroid structure, showcasing the fascinating interplay of chemical modifications. Here are some notable insights:

  • Steroidal Base: This compound is built upon a steroid framework, which is significant because steroids are crucial in various biological processes, including hormone regulation and cellular functions.
  • Functional Groups: The presence of hydroxyl (-OH) and acetate (-OCOCH3) groups indicates its potential reactivity and interaction patterns in biochemical processes.
  • Isomeric Significance: The stereochemistry of the compound, particularly the (17R) stereocenter, can greatly influence its biological activity, making stereochemistry a pivotal aspect in pharmacology and drug design.
  • Natural Occurrence: Compounds similar to this one are often derived from natural sources like plants or microorganisms, suggesting potential applications in natural medicine or therapeutic agents.
  • Research Potential: Due to its structural complexity, this compound may provide a foundation for further research into developing new synthetic methods or studying its interactions within biological systems.

In summary, the compound is not just a simple molecule; it embodies a wealth of scientific inquiry into steroidal structures, functional group chemistry, and biological relevance. Its study can lead to a deeper understanding of both synthetic and natural products in the realm of chemistry.