Skip to main content

Hydrocortisone 17-propionate

ADVERTISEMENT
Identification
Molecular formula
C27H38O7
CAS number
74050-20-7
IUPAC name
(10,13-dimethyl-3-oxo-17-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-16-yl) propanoate
State
State

It is typically found in a solid state at room temperature.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
495.00
Boiling point (Kelvin)
768.15
General information
Molecular weight
514.59g/mol
Molar mass
514.6590g/mol
Density
1.1000g/cm3
Appearence

The compound appears as a white to off-white crystalline powder. It may be odorless or have a faint characteristic odor.

Comment on solubility

Solubility Overview

The compound (10,13-dimethyl-3-oxo-17-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-16-yl) propanoate exhibits unique solubility characteristics that are essential for its applications in chemistry and biochemistry.

Factors Influencing Solubility

Several factors can affect the solubility of this compound:

  • Molecular Structure: The presence of multiple functional groups, particularly the propanoate moiety, can enhance solubility in polar solvents.
  • Hydrophobic Effects: The large hydrophobic regions may lead to decreased solubility in non-polar solvents, indicative of the balance between hydrophilic and hydrophobic properties.
  • Temperature: Solubility often increases with temperature; thus, heating may aid the dissolution process.
  • pH Levels: Changes in pH can influence ionization of functional groups, further modifying solubility in aqueous solutions.

Solubility Summary

In summary, the solubility of this compound can be described as:

  • Moderate to high in polar solvents, such as methanol or ethanol.
  • Lower solubility in non-polar solvents, like hexane or toluene.
  • Temperature-dependent solubility, with increased solubility at elevated temperatures.

Due to these factors, it is crucial to carefully assess the solvent choice when working with this compound in experimental settings. Understanding solubility is vital for effective utilization in formulations and reactions.

Interesting facts

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

This compound belongs to the class of steroids, a fascinating group of organic molecules that play crucial roles in biological processes. Steroids are known for their diverse functions, including acting as hormones and impacting metabolism. Here are some interesting points about this compound:

  • Structural Complexity: The intricate structure of this compound showcases the rich tapestry of organic chemistry. With its multiple rings and functional groups, it highlights the beauty and complexity inherent in steroidal compounds.
  • Biological Relevance: Molecules similar to this compound often play significant roles in endocrine signaling and physiological functions. As a derivative of naturally occurring steroids, it could potentially exhibit similar biological activities.
  • Synthesis and Modifications: The presence of methyl and propanoyloxy groups indicates areas where researchers can modify the compound to explore enhanced biological activity or improved pharmacokinetics. Such modifications are vital for drug development.
  • Potential Therapeutic Use: Given its steroidal nature, this compound might be investigated for applications in therapies related to hormonal imbalances, anti-inflammatory responses, or metabolic issues.
  • Research Implications: Compounds like this one are often the focus of chemistry and pharmacology studies, aiming to understand their mechanisms, enhance their efficacy, and minimize side effects.

As a student of chemistry, exploring such complex structures can be immensely rewarding. By unraveling the specific roles and mechanisms of compounds like this one, we contribute to the broader understanding of chemical interactions within biological systems.

Synonyms
22204-52-0
(10,13-dimethyl-3-oxo-17-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-16-yl) propanoate
16alpha-Hydroxytestosterone dipropionate
NSC-12203
16.alpha.-Hydroxytestosterone dipropionate
Testosterone,dipropionate
hydroxytestosterone propionate
DTXSID50944864
Androst-4-en-3-one, dipropionate
NSC12203
SQ 9718
16.alpha.-Hydroxytestosterone propionate
3-Oxoandrost-4-ene-16,17-diyl dipropanoate
16-ALPHA-HYDROXYTESTOSTERONE DIPROPIONATE
16-.alpha.,17-.beta.-bis(1-oxopropoxy)androst-4-en-3-one
Androst-4-en-3-one,17-bis(1-oxopropoxy)-, (16.alpha.,17.beta.)-