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butyl 4-aminobenzoate

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Identification
Molecular formula
C11H15NO2
CAS number
94-09-7
IUPAC name
butyl 4-aminobenzoate;picric acid
State
State

Butyl 4-aminobenzoate is typically in a liquid state at room temperature.

Melting point (Celsius)
21.00
Melting point (Kelvin)
294.15
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.65
General information
Molecular weight
213.26g/mol
Molar mass
213.2590g/mol
Density
1.1300g/cm3
Appearence

Butyl 4-aminobenzoate appears as a colorless to pale yellow liquid. It is an organic compound often used in pharmaceutical applications.

Comment on solubility

Solubility of Butyl 4-Aminobenzoate and Picric Acid

When considering the solubility of the compound butyl 4-aminobenzoate (C11H15NO2) in various solvents, its characteristics can be quite intriguing:

  • Solvent Compatibility: Butyl 4-aminobenzoate is generally soluble in organic solvents such as alcohols, ethers, and some oils.
  • Polarity: Given its structure, which includes both hydrophobic (butyl group) and hydrophilic (amino group) features, it exhibits moderate solubility in polar solvents like water, but significantly better solubility in less polar solvents.

On the other hand, the solubility of picric acid (C6H3N3O7) showcases different properties:

  • Highly Soluble: Picric acid is known to be highly soluble in water, a characteristic that makes it easily dispersible.
  • Solvent Versatility: It can dissolve in various organic solvents, including alcohols and acetone, which contributes to its versatility in chemical reactions.

In conclusion, the solubility of these compounds highlights their diverse chemical behaviors, influenced by their unique molecular structures. As a rule of thumb, the solubility of organic compounds can often be understood through the aphorism "like dissolves like," where polar substances tend to dissolve in polar solvents, and non-polar substances in non-polar solvents.

Interesting facts

Butyl 4-Aminobenzoate

Butyl 4-aminobenzoate, commonly known as butyl para-aminobenzoate, is an intriguing compound with several applications and properties worth discussing.

  • Chemical Classification: This compound belongs to the family of amides, and its structure features a butyl group attached to the para position of an aminobenzoate.
  • Applications: Butyl 4-aminobenzoate is often used in the production of various pharmaceuticals and as a reagent in organic synthesis, showcasing its versatility.
  • Biological Activity: Some studies have indicated that this compound might exhibit antimicrobial properties, making it a subject of interest in medicinal chemistry.
  • Safety Precautions: As with many chemical compounds, proper handling and safety measures are critical when working with butyl 4-aminobenzoate, especially in laboratory settings.

Researchers often highlight the compound's potential in developing new medicines, as understanding the interactions at a molecular level can lead to breakthroughs in treatment options.

Picric Acid

Picric acid, or 2,4,6-trinitrophenol, is a fascinating compound with a rich history and notable chemical properties.

  • Historical Significance: Originally used as a dye, picric acid found its primary role in World War I as an explosive, highlighting its dual functionality in both civilian and military applications.
  • Explosive Properties: As a nitro compound, picric acid is a powerful explosive. Its sensitivity to shock and heat requires special handling and storage procedures.
  • Medical Uses: In lower concentrations, picric acid has been used in medicine as an antiseptic and in the treatment of various skin conditions.
  • Environmental Concerns: The use of picric acid, particularly in military contexts, has raised environmental and safety concerns, leading to increased scrutiny and regulation.

Because of its intriguing balance between utility and hazard, picric acid continues to be a subject of extensive study in both scientific and safety communities. As scientists delve into the mechanisms of its reactivity, they uncover both its potentials and pitfalls in modern chemistry.

Synonyms
SCHEMBL339139
PD051465