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Isonipecotic acid

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Identification
Molecular formula
C9H11NO2
CAS number
498-94-2
IUPAC name
4-(3-pyridyl)butanoic acid
State
State

At room temperature, isonipecotic acid is generally in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
228.50
Melting point (Kelvin)
501.65
Boiling point (Celsius)
378.50
Boiling point (Kelvin)
651.65
General information
Molecular weight
151.18g/mol
Molar mass
151.1840g/mol
Density
1.1879g/cm3
Appearence

Isonipecotic acid typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-(3-pyridyl)butanoic acid

4-(3-pyridyl)butanoic acid, represented by the chemical formula C9H11NO2, exhibits interesting solubility characteristics. This compound is a carboxylic acid with a pyridine ring, and its solubility can be influenced by several factors.

  • Polarity: The presence of the carboxylic acid group (-COOH) enhances the compound's polarity, suggesting better solubility in polar solvents.
  • Solvent Compatibility: 4-(3-pyridyl)butanoic acid is likely to be soluble in water and other polar solvents, while its solubility in non-polar solvents may be significantly lower.
  • Hydrogen Bonding: The ability of the -COOH group to form hydrogen bonds can contribute to its solubility in aqueous solutions.

As a general observation, many organic compounds that possess functional groups capable of hydrogen bonding (like carboxylic acids) tend to be more soluble in water. Therefore, one might anticipate that 4-(3-pyridyl)butanoic acid would exhibit good solubility in polar solvents including water, while its solubility in organic solvents might be variable. In practical applications, understanding the solubility of such compounds can be crucial for their effective use in pharmaceuticals and agrochemicals.

Interesting facts

Interesting Facts about 4-(3-pyridyl)butanoic Acid

4-(3-pyridyl)butanoic acid is an intriguing organic compound that possesses several remarkable characteristics:

  • Structural Diversity: This compound contains a pyridine ring, contributing to its unique properties and reactivity. Pyridine is known for its ability to participate in various chemical reactions.
  • Biological Significance: Compounds similar to 4-(3-pyridyl)butanoic acid often play roles in biological systems. They can act as metabolic intermediates or be involved in the regulation of enzymatic activities.
  • Potential Therapeutic Uses: Research has suggested that derivatives of this compound may exhibit pharmacological activities, making them candidates for drug development in treating various conditions.
  • Intriguing Synthesis: The synthesis of 4-(3-pyridyl)butanoic acid engages interesting chemical reactions, including the formation of carboxylic acids and amines, which can be valuable for students and chemists looking to deepen their understanding of organic synthesis.
  • Application in Material Science: Due to its distinctive structure, this compound has potential applications in the development of new materials, especially in fields like polymers and nanotechnology.

As characterized by its pyridine moiety, 4-(3-pyridyl)butanoic acid serves as an excellent example of how organic compounds can bridge the gap between chemical synthesis and practical applications, making it a compelling subject for further study.


Synonyms
3-pyridinebutanoic acid
4-(pyridin-3-yl)butanoic acid
4-pyridin-3-ylbutanoic acid
17270-50-7
3-Pyridinebutanoate
4-Pyridin-3-ylbutanoate
4-3-Pyridyl-butanoic acid
4-(3-pyridyl)-butanoic acid
4-3-PYRIDYL-BUTANOATE
477251-67-5
4-(3-pyridyl)-butanoate
4-pyridin-3-yl-butyric acid
MFCD16301159
3-pyridine butanoic acid
4-(Pyridin-3-yl)butanoate
4-(3-pyridyl)-butyric acid
4-(pyridin-3-yl)butanoicacid
4-(3-pyridil)-butanoic Acid
SCHEMBL1583762
CHEMBL3544626
CHEBI:173736
MFYZACBRKCFXDV-UHFFFAOYSA-N
AKOS013528141
DB-136884
CS-0266451
NS00115015
EN300-180999