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Sodium ibuprofen

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Identification
Molecular formula
C13H17NaO3
CAS number
31121-93-4
IUPAC name
sodium;2-[1-(hydroxymethyl)cyclohexyl]acetate
State
State

At room temperature, sodium ibuprofen is in a solid state due to its ionic nature, forming crystalline powders.

Melting point (Celsius)
197.00
Melting point (Kelvin)
470.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
228.26g/mol
Molar mass
228.2610g/mol
Density
1.0090g/cm3
Appearence

Sodium ibuprofen is typically a white to off-white crystalline powder. It is odorless and exhibits high solubility in water which distinguishes it from its acid form.

Comment on solubility

Solubility of Sodium 2-[1-(Hydroxymethyl)cyclohexyl]acetate

Sodium 2-[1-(hydroxymethyl)cyclohexyl]acetate, with its unique structure, exhibits interesting solubility properties. Here are some key points to consider:

  • Water Solubility: This compound is likely to be highly soluble in water due to the presence of the hydroxymethyl group, which is polar and can engage in hydrogen bonding with water molecules.
  • Organic Solvents: Given its amphiphilic nature, it may also dissolve well in some organic solvents. However, it may show variable solubility across different organic phases.
  • pH Dependency: The solubility could be influenced by the pH of the solution. Alkaline conditions might enhance the ionization of the acetate group, potentially increasing solubility.
  • Temperature Effects: Like many compounds, increasing temperature may improve solubility, leading to better molecular interaction and reduced lattice energy in the solid state.

In conclusion, the solubility of sodium 2-[1-(hydroxymethyl)cyclohexyl]acetate is expected to be advantageous for various applications, making it a versatile compound in chemical formulations.

Interesting facts

Interesting Facts about Sodium; 2-[1-(hydroxymethyl)cyclohexyl]acetate

Sodium; 2-[1-(hydroxymethyl)cyclohexyl]acetate is a fascinating compound that merges both organic and inorganic chemistry in a unique way. This compound is actually a salt, which means it is derived from an acid and a base.

Key Highlights:

  • Dual Nature: As a hybrid compound, it possesses characteristics of both acetates and cyclohexyl derivatives, allowing for versatile applications in chemical synthesis.
  • Biological Importance: The presence of the hydroxymethyl group may suggest its relevance in biological systems, potentially influencing various biochemical pathways.
  • Applications: Compounds like this are often researched for their use as intermediates in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.
  • Functional Group Variety: The combination of hydroxymethyl and acetate groups in this molecule enhances its reactivity, opening opportunities for further modifications.

Interestingly, the acetate moiety is a key player in various biological and chemical processes, emphasizing the need for further study in enzyme pathways and interactions. In the realm of chemical education, this compound offers a practical example of how complex organic structures can emerge from simple organic and inorganic building blocks. As noted by leading chemists, “The elegance of chemical bonding can lead to innovations in materials and drug design.”

In conclusion, sodium; 2-[1-(hydroxymethyl)cyclohexyl]acetate is more than just a chemical formula; it represents the intricate dance between different branches of chemistry, showcasing both potential and promise in various scientific fields.