Skip to main content

Testosterone tosylate

ADVERTISEMENT
Identification
Molecular formula
C27H38O4S
CAS number
3653-06-9
IUPAC name
[10,13-dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate
State
State

In its room temperature state, Testosterone tosylate is a solid, specifically existing as a crystalline powder.

Melting point (Celsius)
121.00
Melting point (Kelvin)
394.15
Boiling point (Celsius)
494.20
Boiling point (Kelvin)
767.35
General information
Molecular weight
502.66g/mol
Molar mass
502.7300g/mol
Density
1.0800g/cm3
Appearence

Testosterone tosylate appears as a white crystalline powder. Its purity and crystalline nature make it easily identifiable in its solid form.

Comment on solubility

Solubility of [10,13-dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate

The solubility of the compound [10,13-dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate is influenced by several factors, which may render it partially soluble in certain solvents. Understanding these factors is essential for applications involving the compound.

Key solubility factors:

  • Polarity: Due to the presence of the sulfonate group, the compound displays some polar character, which may enhance solubility in polar solvents, particularly water.
  • Hydrophobic character: The large hydrophobic hydrocarbon-based structure likely limits solubility in water but can lead to preferential solubility in nonpolar organic solvents like hexane or toluene.
  • Temperature: As with many organic compounds, solubility can increase with temperature, thus affecting the compound's dissolution in mobile or heated solvent systems.

In conclusion, while this compound exhibits some polar characteristics due to its sulfonate group, its overall solubility profile is expected to be quite complex due to the combination of polar and nonpolar regions. It's probable that the solubility in various solvents can be best described as:

  1. Moderate in polar solvents due to the sulfonate moiety.
  2. Higher solubility in nonpolar solvents due to its extensive hydrocarbon framework.
  3. Dependent on temperature and the specific solvent used.

Ultimately, understanding the solubility characteristics of this compound will require careful experimentation and analysis to fully delineate its behavior in different environments.

Interesting facts

Interesting Facts about [10,13-Dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate

This compound, with its intricate and extended chemical structure, belongs to a class of compounds known for their unique biochemical interactions. Here are some engaging facts about it:

  • Synthetic Nature: This compound is a synthetic derivative often utilized in the study of receptor binding and pharmacological activities, providing insight into mechanisms of action in various biological systems.
  • Unique Structure: The complex cyclopenta[a]phenanthrene backbone gives this compound interesting attributes, enabling it to interact with numerous targets in the body, such as steroid receptors.
  • Potential Applications: Due to its structure, it may be explored for its potential therapeutic effects, particularly in the fields of endocrinology and cancer research.
  • Substituents Matter: The presence of the 4-methylbenzenesulfonate group can enhance solubility properties and could influence how this compound behaves in biological systems, making it a vital area of research.

As with many compounds of this nature, structure-activity relationships play a crucial role in understanding its effects. Researchers continually aim to uncover the depths of its function:

"Understanding the nuances of molecular interactions is key to unlocking therapeutic potential." - Anonymous

Overall, the compound reflects the fascinating complexity of organic chemistry, bridging synthetic methods with potential real-world applications in medicine and beyond.

Synonyms
(10,13-dimethyl-17-octan-2-yl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl) 4-methylbenzenesulfonate
CHOLESTANE, 3.BETA-(TOSYLOXY)-5.ALPHA-
NSC 93493