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Medroxyprogesterone

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Identification
Molecular formula
C22H30O3
CAS number
520-85-4
IUPAC name
4-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione
State
State

Medroxyprogesterone is typically found as a solid in its powdered form at room temperature. This makes it suitable for its application in pharmaceutical formulations, such as tablets and injectables.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
527.00
Boiling point (Kelvin)
800.15
General information
Molecular weight
386.53g/mol
Molar mass
386.5320g/mol
Density
1.1700g/cm3
Appearence

Medroxyprogesterone appears as a white to off-white crystalline powder. It is often finely granulated and may appear slightly creamy due to its natural form or processing impurities.

Comment on solubility

Solubility of 4-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione (C22H30O3)

The solubility of 4-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione can be quite intriguing due to its complex molecular structure. Understanding its solubility helps in determining how it might behave in various environments, particularly in biological and industrial applications.

Key Factors Influencing Solubility:

  • Molecular Structure: The presence of multiple hydroxy groups often suggests potential for hydrogen bonding, which can enhance solubility in polar solvents.
  • Polarity: The overall polarity of the compound plays a crucial role; more polar compounds tend to dissolve better in polar solvents (like water), while non-polar compounds are more soluble in non-polar solvents (like oils).
  • Temperature: As with many organic compounds, solubility can increase with temperature, particularly in solid form, leading to greater dissolution rates.

Moreover, while this compound may show some degree of solubility in organic solvents due to its hydrocarbon backbone, its polar functional groups may allow for limited solubility in aqueous media. However, specific experimental data are essential to establish its precise solubility characteristics in different solvents. In general, the pattern tends to be:

  1. In organic solvents: Moderate to high solubility.
  2. In water: Likely low solubility.

In conclusion, understanding the solubility of C22H30O3 provides valuable insights into its potential applications and behaviors in various chemical reactions and processes.

Interesting facts

Interesting Facts about 4-Hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

This compound, with its intricate structure, is known for several fascinating properties and applications in the field of organic chemistry. Here are some key points to consider:

  • Complex Structure: The molecular structure features a unique arrangement of hydrocarbon rings, contributing to its classification as a polycyclic aromatic compound.
  • Biological Relevance: Compounds like this one are often examined for their biological activities, particularly in pharmaceutical research. They may exhibit promising properties similar to those of naturally occurring hormones.
  • Synthesis: The synthesis of similar compounds involves advanced techniques in organic synthesis, including steps like reduction, oxidation, and cyclization. Mastery of these techniques is essential for students and chemists alike.
  • Applications: Potential applications in medicinal chemistry and agricultural chemistry make this compound of interest. Its derivatives could serve in drug formulation or as agrochemicals.
  • Research Potential: The ongoing research into compounds with similar frameworks can lead to discoveries in material sciences and new drug development, showcasing the compound's relevance beyond traditional chemistry.

As stated by a renowned chemist, “Chemistry is the ultimate reality, and understanding complex compounds like this is a step toward unlocking the mysteries of life and nature.” Thus, studying such compounds can not only enrich our knowledge of chemistry but also pave the way for significant innovations in various scientific fields.

Synonyms
4-Androsten-4-ol-3,17-dione
NCGC00015070-04
Lopac0_000068
CHEMBL314699
SCHEMBL13838287
CCG-204163
LP00068
SDCCGSBI-0050056.P002
SMP2_000343
NCGC00015070-02
NCGC00015070-03
NCGC00093579-01
NCGC00093579-02
4-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione
DB-052952
EU-0100068
4-OH-A; 4-Hydroxy-4-androstene-3,17-dione
A 5791
SR-01000075670
SR-01000075670-1
625-331-3