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Sulfanilic acid hydrazide

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Identification
Molecular formula
C7H9N3O3S
CAS number
98-16-8
IUPAC name
N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid
State
State

Typically a solid at room temperature.

Melting point (Celsius)
189.00
Melting point (Kelvin)
462.15
Boiling point (Celsius)
732.00
Boiling point (Kelvin)
1 005.15
General information
Molecular weight
215.24g/mol
Molar mass
215.2440g/mol
Density
1.5365g/cm3
Appearence

White to light yellow crystalline powder. The appearance is consistent with many sulfonamide derivatives that possess a degree of crystallinity. It may appear in a slightly off-white shade due to impurities or exposure to air. The compound is typically handled in a solid form for its stability and ease of measurement.

Comment on solubility

Solubility of N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid

N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid, with its complex structure, exhibits intriguing solubility characteristics that are worth exploring. The presence of multiple functional groups significantly influences its solubility profile in various solvents. Here are some key points to consider:

  • Polarity: Due to its sulfonimidic acid and carboxylic acid functionalities, this compound is likely to be highly polar, promoting solubility in polar solvents, such as water.
  • Hydrogen Bonding: The presence of both amino and carboxy groups facilitates hydrogen bonding, enhancing solubility in protic solvents.
  • pH Dependency: This compound may demonstrate variable solubility across different pH levels, where changes in ionization can affect its overall solubility profile.
  • Temperature Influence: The solubility of such compounds often increases with temperature, particularly in aqueous solutions.

In summary, one can speculate that N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid will generally be more soluble in polar solvents, particularly water, due to its polar functional groups and ability to form hydrogen bonds.
Understanding the solubility of this compound can be crucial for its applications in various chemical processes, including synthesis and formulation in pharmaceuticals.

Interesting facts

Interesting Facts about N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid

N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid, also known as a sulfonamide compound, is an intriguing member of the sulfanilamide class known for their medicinal properties. Here are some fascinating aspects of this compound:

  • Antimicrobial Activity: Sulfonamides, including this compound, are recognized for their role as antibiotics. They function by inhibiting bacterial growth, making them valuable in the treatment of various infections.
  • Structural Complexity: The presence of both amino and sulfonamide groups in its structure provides a unique functionality, which can contribute to its versatility in potential pharmacological applications.
  • Potential in Cancer Research: Research has shown that some sulfonamides exhibit anticancer properties, making compounds like N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid of interest in oncological studies.
  • Enzyme Inhibition: This compound is known to interact with specific enzymes, potentially leading to therapeutic effects in treating diseases related to metabolic dysregulation.
  • Commercial Importance: Sulfonamides have been used in various pharmaceutical drugs, and the study of compounds like this one can pave the way for the development of new and improved therapies.

Researchers continue to explore the mechanisms by which N-amino-4-[carboxy(methyl)amino]benzenesulfonimidic acid operates, aimed at uncovering its full potential as a therapeutic agent. As with many compounds in the sulfonamide group, the quest for understanding their full range of applications remains an exciting frontier in the fields of medicinal chemistry and pharmacology.