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Sulfanilamide

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Identification
Molecular formula
C6H8N2O2S
CAS number
63-74-1
IUPAC name
sodium;N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate
State
State

At room temperature, sulfanilamide is in a solid state.

Melting point (Celsius)
164.50
Melting point (Kelvin)
437.65
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
172.20g/mol
Molar mass
172.2040g/mol
Density
1.0800g/cm3
Appearence

Sulfanilamide appears as an off-white to light yellow crystalline powder.

Comment on solubility

Solubility of Sodium N-[5-Amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate

The solubility of sodium N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate can be influenced by several factors, making a thorough understanding essential for practical applications. This compound possesses both sulfonyl and amino functional groups, which contribute to its polar nature. As a result, it exhibits varying degrees of solubility in different solvents.

Key Points Regarding Solubility:

  • Solvent Polarity: The compound is more soluble in polar solvents such as water compared to non-polar solvents, due to its ionic nature when in sodium form.
  • pH Sensitivity: Its solubility may also be pH-dependent, where changes in pH can affect the ionization of the amino groups, thus influencing solubility.
  • Temperature Impact: An increase in temperature often enhances solubility for many compounds, including this one, although specific data should be referenced for precise values.
  • Ionic Strength: The presence of other ions in solution may either enhance or impede solubility by competitive or cooperative interactions.

In summary, sodium N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate exhibits better solubility in polar environments and is susceptible to changes in conditions such as pH and temperature. As noted, “the right context can unlock solubility potential, revealing pathways to innovative applications.”

Interesting facts

Interesting Facts about Sodium; N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate

N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate is a fascinating compound that showcases the intricate interplay of organic and inorganic chemistry. Here are some compelling aspects of this compound:

  • Biological Significance: This compound contains amino groups and sulfonyl functional groups, which are often found in biologically active molecules. Such structures are integral in pharmaceuticals for their role in targeting specific biological pathways.
  • Antimicrobial Properties: Compounds with sulfonamide groups have been widely used in the development of antibiotics. The sulfonyl moieties can enhance the efficacy of these compounds against a range of bacterial infections.
  • Structural Diversity: The combination of multiple functional groups allows for a variety of chemical reactions. Scientists can modify the compound’s structure to improve its properties or to develop new derivatives with enhanced biological activities.
  • Research Potential: Due to its complex structure, this compound is of significant interest in drug design. Researchers explore its interactions at the molecular level, aiding in the discovery of new therapeutic agents.

The study of compounds like N-[5-amino-2-(4-aminophenyl)sulfonyl-phenyl]sulfonylethanimidate not only expands our understanding of medicinal chemistry but also inspires new innovations in the field. As quoted by renowned chemist Dr. Marie Curie, "Nothing in life is to be feared, it is only to be understood." This encapsulates the essence of research in chemistry, where each compound holds the key to unlocking new knowledge.