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Folic acid

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Identification
Molecular formula
C19H19N7O6
CAS number
59-30-3
IUPAC name
2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid
State
State

Folic acid is typically a solid at room temperature.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
757.20
Boiling point (Kelvin)
1 030.40
General information
Molecular weight
441.40g/mol
Molar mass
441.4040g/mol
Density
1.6400g/cm3
Appearence

Folic acid is a yellow or orange-yellow crystalline powder. It can be odorless or may have a slight characteristic odor.

Comment on solubility

Solubility of 2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid (C19H19N7O6)

The solubility of 2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid can be described by its structural characteristics and functional groups. This compound features multiple ionic and polar functional groups, making it quite soluble in various solvents. Here are some key points regarding its solubility:

  • Hydrophilicity: The presence of amino (-NH2) and carboxylic acid (-COOH) groups enhances its ability to interact with water molecules.
  • Solvents: It is expected to be soluble in water and other polar solvents due to these functional groups.
  • Temperature Influence: Like many organic acids, the solubility may increase with temperature, making it more effective in higher temperature conditions.
  • pH Dependency: The solubility can also be influenced by the pH of the solution; in acidic conditions, the carboxylic acid might remain protonated, whereas in neutral or basic conditions, it will dissociate, affecting its solubility behavior.

Overall, the solubility of 2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid is indicative of its potential uses in various chemical and biological applications, highlighting its versatility in aqueous environments.

Interesting facts

Interesting Facts about 2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid

2-[(5-amino-5-carboxy-pentyl)amino]pentanedioic acid, a complex amino acid derivative, plays a vital role in various biochemical processes. Here are some fascinating aspects of this compound:

  • Biological Significance: This compound is a key player in the biosynthesis of important biomolecules, contributing to protein synthesis and metabolic pathways.
  • Functional Groups: Its structure features multiple functional groups, including amino and carboxylic acid groups, which can significantly influence its reactivity and interactions in biological systems.
  • Synthetic Utility: Chemists often employ this compound in synthetic biology and medicinal chemistry for developing new therapeutic agents that target specific enzymes and pathways.
  • Research Applications: Studies have shown that modifications of its structure can lead to enhanced properties, making it a prime candidate for research in drug design and delivery systems.

As you delve deeper into the chemistry of this fascinating compound, remember that every molecule tells a story of its interactions within living organisms and potential applications in science. The exploration of such compounds opens doors to numerous innovations in medicine and biotechnology.

Synonyms
L- Saccharopin
SCHEMBL880791
(5-Amino-5-carboxypentyl)glutamic acid