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Fenofibric acid

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Identification
Molecular formula
C10H13NO2
CAS number
42017-89-0
IUPAC name
2-(4-aminophenyl)butanoic acid
State
State

At room temperature, fenofibric acid is a solid.

Melting point (Celsius)
197.00
Melting point (Kelvin)
470.15
Boiling point (Celsius)
355.40
Boiling point (Kelvin)
628.50
General information
Molecular weight
219.27g/mol
Molar mass
218.2710g/mol
Density
1.2950g/cm3
Appearence

Fenofibric acid appears as a white or almost white crystalline powder. It is odorless or practically odorless and can be sensitive to light. The exact description can vary depending on the form, such as any impurities present or its physical form (powder, crystals, etc.).

Comment on solubility

Solubility of 2-(4-aminophenyl)butanoic acid

2-(4-aminophenyl)butanoic acid, also known as a derivative of amino acids, exhibits intriguing solubility properties due to its structure.

Its solubility can be influenced by several factors, including:

  • pH Level: The solubility of this compound typically increases in acidic conditions. This is because the carboxylic acid group can protonate, leading to increased solubility in polar solvents.
  • Polarity: The presence of both an amino group and a carboxylic acid group makes this compound polar, which contributes to its affinity for polar solvents like water.
  • Hydrogen Bonding: The ability of 2-(4-aminophenyl)butanoic acid to form hydrogen bonds with water molecules enhances its solubility. The amino group (-NH₂) can also participate in hydrogen bonding, adding to the solubility profile.

As a result, it is generally found to be more soluble in aqueous solutions compared to non-polar solvents. However, it should be noted that this solubility can vary depending on concentrations and specific conditions.

In summary, the solubility of 2-(4-aminophenyl)butanoic acid can be highlighted as:

  1. Higher solubility in acidic and polar solvents
  2. Enhanced solubility due to molecular polarity
  3. Increased interaction through hydrogen bonding

Understanding the solubility of this compound is essential for its applications in pharmaceutical and biochemical contexts, where solubility impacts bioavailability and therapeutic effectiveness.

Interesting facts

Interesting Facts about 2-(4-Aminophenyl)butanoic Acid

2-(4-Aminophenyl)butanoic acid, often referred to in scientific literature for its unique structural properties and biological significance, is a fascinating compound in the field of organic chemistry. Here are some intriguing facts that highlight its relevance:

  • Structural Features: This compound has a distinct structure that includes an amino group and a carboxylic acid group, contributing to its reactivity and interactions with biological systems.
  • Biological Importance: It has been studied for its potential therapeutic roles, particularly in relation to its involvement in the synthesis of various pharmaceuticals.
  • Research Applications: The compound serves as a valuable reagent in synthetic organic chemistry. It can be used for the formulation of other more complex molecules in drug development.
  • Mechanism of Action: Some studies suggest that it may influence specific biological pathways, making it a candidate for exploring new treatment options in medicine.
  • Safety Considerations: As with many organic compounds containing amines and acids, safety and handling precautions are paramount during laboratory experimentation.

In summary, 2-(4-aminophenyl)butanoic acid not only serves as an important building block in diverse chemical reactions but also paves the way for advancements in medicinal chemistry and drug discovery. Its synthesis and applications continue to intrigue chemists looking for innovative solutions in health sciences.

Synonyms
2-(4-aminophenyl)butanoic acid
DTXSID201020312
RefChem:456710
DTXCID901777748
608-388-9
29644-97-1
MFCD00598059
Benzeneacetic acid, 4-amino-alpha-ethyl-
BUTYRIC ACID, 2-(p-AMINOPHENYL)-
alpha-(p-Aminophenyl)butyric acid
2-(p-Aminophenyl)butyric acid
Benzeneacetic acid,4-amino-a-ethyl-
NSC 27530
NSC27530
Indobufen Impurity 7
p-aminophenylbutyric acid
-(p-Aminophenyl)butyric acid
SCHEMBL261617
2-(4'-Aminophenyl)butyric acid
WAPLXGPARWRGJO-UHFFFAOYSA-N
1-alpha-(p-Aminophenyl)butyric acid
dl-alpha-(p-Aminophenyl)butyric acid
NSC-27530
AKOS004117910
AKOS016843100
Benzeneacetic acid, 4-amino-|A-ethyl-
DS-16584
SY237659
CS-0152617
C74519
F224529