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Deoxycorticosterone acetate

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Identification
Molecular formula
C24H34O4
CAS number
103-23-1
IUPAC name
17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
State
State

At room temperature, deoxycorticosterone acetate is in a solid state. It is typically encountered as a crystalline powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
374.54g/mol
Molar mass
374.5390g/mol
Density
1.1750g/cm3
Appearence

Appearance: Deoxycorticosterone acetate is a white or nearly white crystalline powder. It is odorless or has a slight, characteristic odor.

Comment on solubility

Solubility of 17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one (C24H34O4)

The solubility of 17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one is an intriguing aspect to consider. This compound, characterized by its complex organic structure, presents specific solubility properties influenced by its chemical features.

Factors Affecting Solubility

Understanding its solubility involves assessing various factors:

  • Polarity: Due to the presence of hydroxyl groups (-OH), the compound exhibits polar characteristics, enhancing solubility in polar solvents.
  • Chain Length: The long aliphatic chain can create hydrophobic interactions, making it less soluble in non-polar solvents.
  • Temperature: Solubility may increase with temperature, affecting the rate of dissolution.

General Solubility Insights

In general, one might find:

  • This compound is likely soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO).
  • It may exhibit limited solubility in water, given its non-polar characteristics aside from the hydroxyl groups.

In summary, the solubility of C24H34O4 is a balance between its polar and non-polar features, making it soluble in certain organic solvents while remaining less soluble in polar environments such as water. Thus, the solubility can be described as selective based on the solvent used.

Interesting facts

Interesting Facts about 17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

This compound, a member of the family of steroid derivatives, exhibits several intriguing characteristics and potential applications that make it a subject of study in various fields of chemistry and biology.

Key Features of the Compound:

  • Steroid Structure: As a complex steroid derivative, it shares structural similarities with natural hormones which are pivotal in many biological processes.
  • Potential Biological Activity: Compounds like these often demonstrate varied biological activities, including anti-inflammatory, anticancer, or neuroprotective effects, which are explored in drug design.
  • Acetyl Group Influence: The presence of the acetyl group can significantly modify the compound's reactivity and solubility, enhancing its pharmacological properties.
  • Hydroxyl Group Role: The hydroxyl (-OH) group is known to increase the compound’s interaction with biological systems, acting as a potential site for further modification or reaction.

Moreover, the complex nomenclature of this compound typically reflects its structural intricacy, revealing information about its functional groups, stereochemistry, and potential reactivity patterns. As scientists continue to study such compounds, they often quote, “A detailed understanding of a compound’s structure is fundamental to predicting its behavior.” This principle is especially true in organic and medicinal chemistry, where small changes in structure can lead to vastly different biological responses.

In conclusion, the exploration of 17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one opens doors to significant advancements in pharmaceuticals, underscoring the importance of understanding complex organic molecules in driving innovation.

Synonyms
11-hydroxy-6-methylpregn-4-ene-3,20-dione
DTXSID60859758
AKOS015961132
AC-13158