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Piracetam

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Identification
Molecular formula
C6H10N2O2
CAS number
7491-74-9
IUPAC name
N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide
State
State

At room temperature, Piracetam is a solid.

Melting point (Celsius)
151.50
Melting point (Kelvin)
424.70
Boiling point (Celsius)
333.30
Boiling point (Kelvin)
606.50
General information
Molecular weight
142.16g/mol
Molar mass
142.1590g/mol
Density
1.3000g/cm3
Appearence

Piracetam is typically a white or almost white crystalline powder that has no distinct odor.

Comment on solubility

Solubility of N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide

N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide, also known as a specific amide compound, presents a fascinating profile when it comes to its solubility characteristics. Understanding solubility is crucial for both chemical applications and pharmaceutical formulations.

In general, the solubility of this compound can be influenced by several factors:

  • Polarity: The presence of the polar acetamide group tends to enhance solubility in polar solvents such as water.
  • Hydrophobicity: The phenyl group contributes to hydrophobic character, potentially limiting solubility in highly polar solvents but increasing solubility in organic solvents.
  • Temperature: Like many organic compounds, its solubility can increase with temperature, allowing more efficient dissolution.
  • pH Dependence: Depending on the pH of the solution, protonation or deprotonation could significantly impact solubility, particularly in aqueous environments.

It is often noted that, "like dissolves like," which indicates that polar solvents will typically dissolve polar solutes, while non-polar solvents will effectively dissolve non-polar substances. Thus, finding the right solvent remains pivotal for maximizing solubility.

In summary, while N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide is expected to show variable solubility based on environmental conditions, careful consideration of factors such as polarity, temperature, and pH can lead to successful outcomes in practical applications.

Interesting facts

Interesting Facts about N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide

N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide, often referred to in the scientific community for its notable properties, is a fascinating compound with various applications. Below are some intriguing aspects that highlight its significance:

  • Pharmaceutical Potential: This compound falls within the realm of medicinal chemistry, where it is analyzed for potential therapeutic uses, particularly in the development of novel analgesics or anti-inflammatory drugs.
  • Structural Characteristics: The unique architecture of N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide features a pyrrolidine ring, which is known to enhance the bioavailability of drugs due to its ability to improve solubility and permeability.
  • Neurotransmitter Interaction: With the presence of the pyrrolidine moiety, studies suggest that it may interact with various neurotransmitter systems, making it a compound of interest in neuropharmacology.
  • Research on Analogues: Scientists often explore analogues of this compound to evaluate how slight modifications in chemical structure can lead to enhanced efficacy or reduced side effects in pharmaceuticals.
  • Multi-functional Properties: Its ability to act in different biological pathways opens doors for multi-functional drug design, where compounds can address several targets in a single molecule.

In summary, N-(1-methylpyrrolidin-3-yl)-N-phenyl-acetamide serves as an exemplary illustration of how synthetic compounds can bridge gaps in medicine and chemistry, inspiring further exploration of their potential applications in the modern scientific landscape.