Skip to main content

Testosterone heptanoate

ADVERTISEMENT
Identification
Molecular formula
C26H40O3
CAS number
315-37-7
IUPAC name
(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate
State
State

At room temperature, testosterone heptanoate is typically a solid in the form of a crystalline powder.

Melting point (Celsius)
33.00
Melting point (Kelvin)
306.20
Boiling point (Celsius)
542.30
Boiling point (Kelvin)
815.50
General information
Molecular weight
400.60g/mol
Molar mass
400.6030g/mol
Density
1.0640g/cm3
Appearence

Testosterone heptanoate is typically a white or creamy white crystalline powder. It is often supplied in the form of fine, raw crystals.

Comment on solubility

Solubility of (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate (C26H40O3)

The solubility of (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate is influenced by several factors, primarily its chemical structure and the presence of functional groups. Here are key considerations regarding its solubility:

  • Polarity: With a notable hydrophobic hydrocarbon backbone, this compound is expected to exhibit low solubility in polar solvents such as water.
  • Solvent Compatibility: It may be more soluble in organic solvents like ethanol, methanol, or chloroform due to non-polar characteristics.
  • Temperature Dependency: The solubility might increase with temperature, as is common for many organic compounds.
  • Concentration Impact: At higher concentrations, aggregation effects might occur, further influencing solubility.

As mentioned in solubility studies, "like dissolves like," indicating that similar types of solutes and solvents will interact favorably. Therefore, understanding the solubility profile is crucial for applications and formulations involving this compound.

Interesting facts

Interesting Facts about (10,13-Dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) Heptanoate

This compound is a fascinating example of how complex organic chemistry can become, especially within the category of steroid derivatives and related compounds. Its structure indicates significant biological relevance, particularly in the realm of hormone synthesis and pharmacology. Here are some intriguing points about this compound:

  • Steroid Framework: The core structure of this compound suggests it may play a role similar to that of steroid hormones, influencing various biological processes.
  • Dimethyl Substituents: The presence of dimethyl groups at specific positions may enhance biochemical activity or alter the compound’s interaction with biological targets.
  • Heptanoate Component: The heptanoate moiety indicates potential application as an ester, which could affect the compound's solubility and permeability in biological systems.
  • Potential Applications: Research into similar compounds has shown promise in drug design, particularly in developing new therapies for hormonal disorders or cancer treatments.
  • Derivative Exploration: Chemists are often excited to explore derivatives of this compound to synthesize new compounds with improved efficacy or reduced side effects.
  • Biological Activity: Although specific studies targeting this compound may be limited, many steroid-like compounds display significant biological activity, making them crucial for investigation.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." Exploring compounds like this can inspire new paths of scientific inquiry and innovation, opening doors to discoveries that may ultimately benefit human health.

In summary, (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate stands as a testament to the complex and often beautiful nature of chemical compounds, promising vast potential for future research.

Synonyms
SCHEMBL18437534
DTXSID30861868
3-Oxoandrost-4-en-17-yl heptanoate