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Solifenacin succinate

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Identification
Molecular formula
C23H26ClNO4
CAS number
242478-37-1
IUPAC name
2-methylsulfonyloxyethyl-[2,3,4,5-tetrahydroxy-6-(2-methylsulfonyloxyethylamino)hexyl]ammonium;chloride
State
State
Solid at room temperature.
Melting point (Celsius)
108.00
Melting point (Kelvin)
381.20
Boiling point (Celsius)
202.50
Boiling point (Kelvin)
475.70
General information
Molecular weight
480.54g/mol
Molar mass
480.5420g/mol
Density
1.3200g/cm3
Appearence

A white to off-white crystalline powder.

Comment on solubility

Solubility of 2-methylsulfonyloxyethyl-[2,3,4,5-tetrahydroxy-6-(2-methylsulfonyloxyethylamino)hexyl]ammonium;chloride

The solubility of the compound 2-methylsulfonyloxyethyl-[2,3,4,5-tetrahydroxy-6-(2-methylsulfonyloxyethylamino)hexyl]ammonium;chloride can be quite intriguing due to its complex molecular structure. Several factors influence its solubility:

  • Polarity: The presence of multiple hydroxyl groups (-OH) suggests that the compound is likely to exhibit considerable polarity, which generally enhances solubility in polar solvents such as water.
  • Ammonium Group: The ammonium component may also contribute to its solubility in aqueous solutions, as ammonium salts are typically soluble.
  • Methylsulfonyloxy Groups: The presence of methylsulfonyloxy groups can introduce additional interactions with solvent molecules, potentially influencing the overall solubility.

As a result of these factors, one might expect this compound to be:

  1. Highly soluble in water due to its ionic nature and polar functional groups.
  2. Less soluble in non-polar solvents, as its structure is not conducive to strong interactions with such solvents.

In conclusion, understanding the solubility characteristics of this complex compound can aid in determining its applications and behavior in various chemical environments. As always, empirical testing remains the best approach to definitively ascertain solubility in different media.

Interesting facts

Interesting Facts about 2-Methylsulfonyloxyethyl-[2,3,4,5-tetrahydroxy-6-(2-methylsulfonyloxyethylamino)hexyl]ammonium Chloride

This fascinating compound is notable for its complex structure and potential applications in various fields. Here are some engaging insights:

  • Complex Arrangement: The structure of this compound contains multiple functional groups, including hydroxyl and sulfonyl groups, which make it highly versatile and reactive.
  • Biological Relevance: Compounds with ammonium functionalities are often studied for their biological activity. This specific compound could play a role in drug development, particularly in targeting specific cellular pathways.
  • Solubility Characteristics: Given its multi-functional nature, it is believed to exhibit interesting solubility characteristics, which can affect its behavior in both aqueous and organic environments.
  • Potential Uses: This compound holds promise in applications related to pharmaceuticals, agriculture, and even materials science due to its unique chemical properties and potential for customization.
  • Structure-Activity Relationship: Scientists are particularly interested in how modifications to the structure, such as variations in the methylsulfonyloxy groups, can influence its chemical reactivity and biological activity. This creates a vast area of research for organic chemists.

In summary, the compound 2-methylsulfonyloxyethyl-[2,3,4,5-tetrahydroxy-6-(2-methylsulfonyloxyethylamino)hexyl]ammonium chloride represents a remarkable intersection of chemistry and biology. As research continues, its various properties may unlock new pathways in science and technology.

Synonyms
1446-35-1
D-Mannitol, 1,6-dideoxy-1,6-bis((2-hydroxyethyl)amino)-, 1,6-dimethanesulfonate (ester), dihydrochloride
R 49