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Testosterone benzoate

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Identification
Molecular formula
C26H38O3
CAS number
5721-91-5
IUPAC name
[17-(1,5-dimethylhexyl)-10,13-dimethyl-2,3,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate
State
State
At room temperature, testosterone benzoate is a solid.
Melting point (Celsius)
193.50
Melting point (Kelvin)
466.60
Boiling point (Celsius)
405.80
Boiling point (Kelvin)
678.90
General information
Molecular weight
414.62g/mol
Molar mass
414.6220g/mol
Density
1.1000g/cm3
Appearence
Testosterone benzoate is typically a white or almost white crystalline powder. It may have a slightly creamy tint, depending on specific purity and manufacturing processes.
Comment on solubility

Solubility of [17-(1,5-dimethylhexyl)-10,13-dimethyl-2,3,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate

The solubility of the compound [17-(1,5-dimethylhexyl)-10,13-dimethyl-2,3,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate is primarily influenced by its chemical structure and the presence of various functional groups. Here are some key points to consider:

  • Polarity: The compound features both hydrophobic (non-polar) and hydrophilic (polar) regions, which impacts its solubility in different solvents.
  • Solvent Interaction: Generally, non-polar compounds demonstrate better solubility in non-polar solvents (e.g., hexane, toluene), while polar solvents (e.g., water, ethanol) may not effectively dissolve it.
  • Alkyl Substituents: The presence of long alkyl chains can enhance solubility in organic solvents but may limit solubility in aqueous environments.
  • Temperature Effects: As temperature increases, solubility can also change, often increasing in organic solvents.

In conclusion, while it may dissolve readily in an appropriate organic solvent, its limited solubility in water suggests it is likely more suited for applications in non-aqueous environments. This compound exemplifies how molecular structure plays a crucial role in determining solubility properties.

Interesting facts

Interesting Facts about [17-(1,5-dimethylhexyl)-10,13-dimethyl-2,3,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] Benzoate

This compound is a complex organic molecule that belongs to the family of steroids and exhibits fascinating properties. Here are some intriguing aspects of this structure:

  • Structural Complexity: The compound features multiple methyl groups and a decahydronaphthylene core, which contributes to its unique 3D shape and steric effects.
  • Biological Relevance: Many compounds like this one are studied for their potential biological activity, impacting hormone regulation and other physiological functions.
  • Pseudosteroid Activity: Its structure suggests potential interaction with steroid receptors, prompting research into its pharmacological effects and therapeutic applications.
  • Benzoate Group: The benzoate moiety can add hydrophobic properties, influencing the compound's interactions in biological systems.

As a chemistry student or researcher, exploring such compounds can lead to a deeper understanding of chemical reactivity and biological mechanisms. One quote that resonates in such studies is, "The beauty of chemistry lies in its ability to blend intricate structures with profound functions."

Overall, this compound serves as an exciting subject in organic chemistry and medicinal research, urging scientists to unravel its mysteries while considering its potential implications in pharmacology and biotechnology.

Synonyms
4,6-Cholestadien-3beta-ol, benzoate
25485-34-1
EINECS 247-021-3
Cholesta-4,6-dien-3-ol, benzoate, (3beta)-
Cholesta-4,6-dien-3-ol, 3-benzoate, (3beta)-
RefChem:576059
Cholesta-4,6-dien-3-ol, 3-benzoate, (3.beta.)-
Cholesta-4,6-dien-3beta-yl benzoate
Cholesta-4,6-dien-3-ol, benzoate, (3.beta.)-
DTXSID80948370
KJRLFFDMSLSIGS-UHFFFAOYSA-N
cholesta-4,6-dien-3-yl benzoate
AKOS024419883
CHOLESTA-4,6-DIEN-3-BETA-YL BENZOATE