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Sodium taurocholate

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Identification
Molecular formula
C26H44NO7SNa
CAS number
145-42-6
IUPAC name
sodium;2-[4-(3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoylamino]ethyl sulfate
State
State

At room temperature, sodium taurocholate is in a solid state, typically appearing as a crystalline powder.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
537.69g/mol
Molar mass
537.6940g/mol
Density
1.2900g/cm3
Appearence

Sodium taurocholate is a white or off-white solid powder.

Comment on solubility

Solubility of Sodium 2-[4-(3,7-Dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoylamino]ethyl Sulfate

The solubility of sodium 2-[4-(3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoylamino]ethyl sulfate is an intriguing aspect of this compound.

Factors influencing its solubility include:

  • Ionic Nature: The presence of sodium ions suggests that this compound may be soluble in polar solvents like water, as ionic compounds tend to dissociate in solution.
  • Molecular Structure: The complex organic structure may hinder solubility in non-polar solvents due to steric hindrance.
  • Hydroxyl Groups: The presence of multiple hydroxyl (–OH) groups can improve solubility by enhancing hydrogen bonding with water molecules.

Overall, while the ionic dopamine-derivative nature of this compound may promote solubility in aqueous environments, the large hydrophobic hydrocarbon part could limit its overall aqueous solubility. Therefore, one might expect to see variable solubility based on the specific conditions, such as temperature and pH. As always, experimental data will provide the most reliable insights.

Interesting facts

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

This compound, a complex sulfated derivative, presents a fascinating intersection of organic synthesis and biological activity. Here are some key facts to note:

  • Biological Relevance: Compounds like this one are often investigated for their potential pharmacological properties. Their structural complexity can lead to unique interactions with biological systems.
  • Structural Diversity: The presence of a cyclopenta[a]phenanthrene framework suggests that this compound might exhibit interesting properties such as enhanced stability or specific binding affinity due to its rigid structure.
  • Functional Groups: The sulfonation and hydroxylation enhance solubility in biological systems, likely allowing it to cross cellular membranes more efficiently, an essential feature for any potential therapeutic agent.
  • Application Potential: Such compounds are often explored in the field of drug design. The sulfation can modify the compound's pharmacokinetic properties, leading to unique methods of delivery in drug therapies.
  • Chemical Synthesis: Its preparation may involve lengthy synthesis routes, often requiring specialized techniques in organic chemistry to achieve the final product.

As noted by renowned chemist Marie Curie, “Nothing in life is to be feared, it is only to be understood.” This encapsulates the excitement of studying such intricate compounds. With ongoing research in the realms of medicinal chemistry and drug development, compounds like this one are at the forefront of discovering new treatments for various diseases.

Exploring such a compound not only enriches our understanding of chemistry but also opens pathways to significant scientific advancements.