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Cholecalciferol sulfate

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Identification
Molecular formula
C32H52O8S
CAS number
155045-48-2
IUPAC name
[10,13-dimethyl-2,3-disulfooxy-17-(1,4,5,5-tetramethylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl] hydrogen sulfate
State
State

At room temperature, cholecalciferol sulfate is in a solid state, generally available as a powder. It retains its solid form and does not transition to a liquid or gas under typical storage conditions.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.00
Boiling point (Celsius)
398.00
Boiling point (Kelvin)
671.00
General information
Molecular weight
622.82g/mol
Molar mass
622.8200g/mol
Density
1.0000g/cm3
Appearence

Cholecalciferol sulfate appears as a solid, usually crystalline powder. The color can range from white to slightly off-white. It is known to be odorless.

Comment on solubility

Solubility of 10,13-dimethyl-2,3-disulfooxy-17-(1,4,5,5-tetramethylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl] hydrogen sulfate

The solubility characteristics of this complex compound with the formula C32H52O8S are influenced by several factors due to its intricate structure:

  • Polarity: The presence of sulfooxy groups affects the overall polarity of the molecule, likely making it more soluble in polar solvents.
  • Hydrogen Bonding: The functional groups can engage in hydrogen bonding, facilitating its dissolution in various solvents.
  • Hydrophobicity: The large hydrophobic carbon chains within the structure may hinder solubility in pure water, suggesting a preference for organic solvents.

It is important to note that such compounds tend to exhibit varying solubility profiles depending on:

  • The temperature of the solvent
  • The presence of other chemical species in the solution
  • The pH of the environment

In summary, understanding the solubility of this compound can be complex, engaging both the hydrophilic and hydrophobic natures stemming from its molecular structure. As a rule of thumb, the more polar the solvent, the greater the solubility of compounds containing polar functional groups. Yet, this compound's substantial lipid character could pose challenges in aqueous environments, leading to solubility challenges in practical applications.

Interesting facts

Interesting Facts about 10,13-dimethyl-2,3-disulfooxy-17-(1,4,5,5-tetramethylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl Hydrogen Sulfate

This fascinating compound, with a lengthy name and a complex structure, represents a unique class of chemicals that highlights the intricacies of organic synthesis. Here are some intriguing aspects worth noting:

  • Structural Complexity: The compound features a polycyclic framework, which is not only robust but plays a crucial role in its potential biological activities. The structure includes multiple substituents, adding to its reactivity and interactions.
  • Sulfonate Groups: The inclusion of disulfooxy functional groups is significant. These sulfonate moieties can influence solubility and ionization, affecting how the compound behaves in various environments, particularly in biological systems.
  • Potential Applications: Due to its intricate structure and reactive sites, such compounds have theoretical applications in fields such as pharmacology, where they may exhibit unique properties that could lead to drug development.
  • Synthetic Interest: Chemists show great interest in synthesizing such complex compounds. The synthesis challenges involved stimulate a lot of creativity and innovation in the laboratory.
  • Biological Relevance: Compounds with similar frameworks are often investigated for hormonal activities or as precursors to more biologically active substances, making them vital for research into endocrinology.

As a remarkable specimen in the realm of organic chemistry, the study of this compound opens the doors to a wealth of knowledge about structure-function relationships in chemical entities. It exemplifies the delicate balance of synthesis, reactivity, and potential for discovery in modern chemistry.