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Acetazolamide Sodium

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Identification
Molecular formula
C4H4N4O3S2Na
CAS number
67-97-0
IUPAC name
sodium;(5-acetamido-1,3,4-thiadiazol-2-yl)sulfonylazanide
State
State

At room temperature, Acetazolamide Sodium is in a solid state as a crystalline powder.

Melting point (Celsius)
258.00
Melting point (Kelvin)
531.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
222.24g/mol
Molar mass
222.2430g/mol
Density
1.7300g/cm3
Appearence

Acetazolamide Sodium appears as a white to off-white crystalline powder. It is fairly soluble in water and has a slightly bitter taste.

Comment on solubility

Solubility of Sodium (5-Acetamido-1,3,4-thiadiazol-2-yl)sulfonylazanide

The solubility characteristics of Sodium (5-Acetamido-1,3,4-thiadiazol-2-yl)sulfonylazanide are essential for understanding its potential applications and behavior in various environments. This compound, due to its ionic nature, generally exhibits favorable solubility in water.

Key Points About Solubility:

  • Polarity: As a sulfonamide derivative, it possesses polar functional groups that enhance interaction with water, leading to increased solubility.
  • Temperature Effect: Solubility can be influenced by temperature; typically, higher temperatures may increase solubility for many salts.
  • pH Sensitivity: The solubility can vary with changes in pH, as the presence of acidic or basic conditions may affect the ionization of the compound.
  • Solvent Choice: While water is the primary solvent, the presence of other solvents (e.g., ethanol or dimethyl sulfoxide) might also affect solubility.

Overall, the solubility of this compound highlights its utility in biochemical applications, where it may readily dissolve and interact with biological systems, often underscored by the statement: "The more soluble a compound, the greater its accessibility for biological reactions." Understanding these solubility dynamics enables chemists to harness the compound effectively in their respective fields.

Interesting facts

Interesting Facts about Sodium (5-Acetamido-1,3,4-thiadiazol-2-yl) Sulfonylazanide

This fascinating compound embodies the intricate relationship between chemistry and biological applications. As a sulfonamide derivative, it showcases unique properties that have drawn the attention of researchers and scientists alike. Here are some key points that highlight its significance:

  • Pharmaceutical Relevance: The presence of the sulfonyl group combined with the thiadiazole moiety opens doors to potential applications in medicinal chemistry. Compounds like this one are often investigated for their antimicrobial and anti-inflammatory properties.
  • Structural Complexity: With its multi-functional structure, this compound demonstrates the beauty of chemical synthesis. The acetamido group contributes to its ability to form hydrogen bonds, potentially enhancing its biological activity.
  • Versatile Applications: Beyond pharmaceuticals, compounds containing thiadiazole rings are also being explored for use in agricultural chemistry, serving as fungicides or herbicides, which further broadens its scope.
  • Mechanistic Insight: Understanding how this compound interacts at the molecular level can contribute to the development of new drugs. Researchers often study the mechanisms by which such compounds inhibit bacterial enzymes.
  • Continual Research: Ongoing studies on the efficacy and safety profiles of new sulfonamide derivatives indicate that the potential of this compound is far from exhausted. Each modification can lead to a better therapeutic agent.

In summary, sodium (5-acetamido-1,3,4-thiadiazol-2-yl) sulfonylazanide is more than just a chemical formula; it represents a promising area of study with implications in healthcare and beyond. As researchers dive deeper into its capabilities, we may soon witness innovative applications stemming from this unique compound!