Skip to main content

Captopril

ADVERTISEMENT
Identification
Molecular formula
C9H15N3O2S2
CAS number
62571-86-2
IUPAC name
2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid
State
State

At room temperature, Captopril is typically found in a solid state as a crystalline powder.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
217.28g/mol
Molar mass
217.2810g/mol
Density
1.4173g/cm3
Appearence

Captopril appears as a white to off-white crystalline powder. It is often used in pharmaceutical formulations and may have a slightly sulfurous odor due to its thiol group.

Comment on solubility

Solubility of 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid

The solubility of 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid (C9H15N3O2S2) is an essential characteristic that influences its applications and efficacy. Understanding its solubility behavior can provide insights into its chemical nature and potential uses.

Factors Influencing Solubility:

  • Polarity: The presence of polar functional groups like -NH2 and -COOH can enhance solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability of this compound to form hydrogen bonds can increase solubility in aqueous solutions.
  • Temperature: Solubility often increases with temperature; therefore, heating may enhance the dissolution rate.
  • pH: The ionization of acidic and basic groups can significantly affect solubility; adjusting the pH may improve solubility in certain environments.

In general, it has been observed that compounds containing both hydrophilic and hydrophobic regions tend to have limited solubility in pure water but can show good solubility in mixed solvents or organic solvents. As a result, the specific solubility of 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid needs to be empirically determined under varying conditions for practical applications. Ultimately, an understanding of its solubility is crucial for its formulation in medicinal chemistry and related fields.

Interesting facts

Interesting Facts about 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid

This compound is an intriguing member of the amino acids family, specifically classified as a modified amino acid, with noteworthy properties and potential applications. Here are some engaging facts:

  • Unique Structure: The presence of both sulfanyl groups in the molecular structure provides interesting reactivity and bonding possibilities that are not typically found in standard amino acids.
  • Pharmacological Research: Given its complex arrangement, this compound has potential implications in medicinal chemistry, especially in the area of drug design where sulfur-containing compounds are gaining attention for their biological activities.
  • Versatile Synthesis: The synthesis of this compound often involves various organic reactions, showcasing the versatility of synthetic methodologies in modern organic chemistry. Such reactions can include amide coupling and carbon-sulfur bond formation.
  • Biological Relevance: As a derivative of propanoic acid, it may also be explored for its role in metabolic pathways and its interactions with enzymes, offering insights into metabolic engineering.
  • Potential Applications: With its unique characteristics, this compound could be relevant in fields such as pharmaceuticals, agrochemicals, and nutraceuticals, especially in the development of innovative therapeutic agents.

In summary, 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid presents a fascinating area for research within chemistry and biology. Its structural features and potential applications underscore the richness of the chemical landscape that modern scientists explore.