1-Deoxymycosterone | Solubility of Things

Identification

Molecular formula

C₂₇H₄₆O₃

CAS number

3884-87-7

IUPAC name

17-(1,5-dimethylhexyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,12-triol

State

At room temperature, 1-Deoxymycosterone is in a solid state, commonly appearing as a crystalline powder.

Melting point (Celsius)

204.00

Melting point (Kelvin)

477.15

Boiling point (Celsius)

457.60

Boiling point (Kelvin)

730.75

General information

Molecular weight

414.68g/mol

Molar mass

414.6840g/mol

Density

1.1890g/cm³

Appearence

1-Deoxymycosterone appears as a white to off-white crystalline powder. It is typically odorless and has a bitter taste if tasted directly.

Comment on solubility

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

The solubility of the compound with the chemical formula C₂₇H₄₆O₃—a complex polycyclic structure—is an intriguing subject due to its unique molecular characteristics.

Given its large hydrophobic (non-polar) carbon framework, it is likely to exhibit poor solubility in water. Here are some points to consider:

Hydrophobicity: The presence of multiple carbon chains suggests that the compound is predominantly hydrophobic, which tends to limit its solubility in polar solvents like water.
Hydrophilicity: The presence of three hydroxyl (–OH) groups introduces a certain level of hydrophilicity; however, their effects may be overshadowed by the extensive hydrophobic regions.
Solvent Compatibility: It is anticipated that the compound may dissolve more readily in non-polar solvents (e.g., hexane, chloroform) rather than polar solvents, reflecting its organic nature.

In summary, while the hydroxyl groups may offer some potential for solubility in polar mediums, the overall solubility of C₂₇H₄₆O₃ is expected to be quite limited in aqueous environments. As a result, this compound is more soluble in organic solvents, making it crucial for applications that require non-polar solvents for dissolution.

Interesting facts

Interesting Facts about 17-(1,5-Dimethylhexyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,12-triol

This remarkable compound falls into the category of steroids, specifically a type of polycyclic compound, which is characterized by multiple interconnected ring structures. Its complex chemical name highlights the intricate nature of its molecular architecture, featuring a total of 27 carbon atoms, which influences its physical and biological properties.

Key Characteristics

Structure Variety: The extensive number of rings and substituents in its structure suggests potential for unique spatial configurations, which can affect its biological activity.
Biological Importance: Compounds like this are often investigated for their relationships with hormones, making them significant in biochemistry and medicinal chemistry.
Research Interest: The stabilization of specific structural motifs may yield insights into the development of pharmaceuticals, particularly in the realm of steroid medicine and treatment of hormonal disorders.

Comments from researchers often include sentiments like, "This compound opens doors to innovative therapeutic strategies," reflecting ongoing interest in its applications.

Furthermore, its comprehensive molecular makeup can impact interactions across biological systems, leading to studies aimed at understanding mechanisms by which such compounds might exert their effects at the cellular level.

Overall, this compound stands as a testament to the complexities and possibilities within organic chemistry, pushing the boundaries of our understanding of chemical biology.