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Beta-Ecdysterone

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Identification
Molecular formula
C27H44O7
CAS number
5289-74-7
IUPAC name
(3S)-17-(1,5-dimethylhexyl)-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5-diol
State
State
Beta-Ecdysterone is solid at room temperature. It appears as a crystalline powder, making it suitable for use in various formulations and applications.
Melting point (Celsius)
240.00
Melting point (Kelvin)
513.20
Boiling point (Celsius)
518.20
Boiling point (Kelvin)
791.40
General information
Molecular weight
480.67g/mol
Molar mass
480.6650g/mol
Density
1.2300g/cm3
Appearence

Beta-Ecdysterone is a white to off-white crystalline powder. It is typically found as a solid in purified form, often utilized in research and supplements.

Comment on solubility

Solubility of (3S)-17-(1,5-dimethylhexyl)-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5-diol

The solubility of this complex organic compound can be quite intriguing due to its intricate structure. As a polycyclic compound with multiple substituents, its solubility is influenced by several factors:

  • Functional Groups: The presence of hydroxyl (–OH) groups typically enhances solubility in polar solvents, such as water.
  • Hydrophobic Regions: The large hydrocarbon chain and polycyclic structure contribute to significant hydrophobic characteristics which typically limit solubility in polar solvents.
  • Solvent Type: Solubility can vary greatly between different solvents. Slightly polar—such as alcohols or ethers—may dissolve this compound more readily than water.

It is often said that "like dissolves like," which suggests that to maximize solubility, one should consider matching the chemical nature of the solvent with that of the solute.

In general, for this compound, you might anticipate:

  1. Low solubility in water due to its large hydrophobic regions.
  2. Better solubility in organic solvents like chloroform or ethanol due to the presence of hydroxyl groups that can interact with polar properties.

Ultimately, the solubility of this compound reflects a balance between its hydrophilic and hydrophobic characteristics, making it an interesting subject for further exploration.

Interesting facts

Interesting Facts About (3S)-17-(1,5-dimethylhexyl)-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5-diol

The compound known as (3S)-17-(1,5-dimethylhexyl)-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5-diol is a remarkable member of the steroid family, showcasing the complexity and diversity of organic compounds. Here are some compelling insights:

  • Steroidal Structure: This compound features a unique tetradecahydrocyclopenta[a]phenanthrene backbone, which is derived from the steroid structure. Steroids are known for their role in various biological functions, including hormones and cellular processes.
  • Functional Groups: The presence of hydroxyl (-OH) groups in its structure indicates that this compound may exhibit important biochemical activities. Hydroxyl groups are often involved in hydrogen bonding, influencing solubility and interaction with biological receptors.
  • Potential Applications: Given its steroid-like characteristics, this compound could exhibit potential in medicinal chemistry. Research continues into the development of steroid derivatives for therapeutic uses.
  • Chirality: Chirality is an essential aspect of this compound. The (3S) designation indicates a specific configuration at a chiral center, which can significantly affect its biological activity and interaction with living organisms.
  • Natural Occurrence: Compounds with similar steroidal structures are often found naturally in plants and animals, hinting at potential uses in natural product chemistry and pharmacognosy.

As scientists explore the vast landscapes of chemical compounds, understanding the nuances of structures like this one becomes essential. The complexity of (3S)-17-(1,5-dimethylhexyl)-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5-diol not only captivates researchers but also opens doors to a myriad of possibilities in drug discovery and development.

Synonyms
Cholestane-3,5-diol
DTXSID70955098