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Glutarylglutamic acid

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Identification
Molecular formula
C11H18N2O7
CAS number
36344-14-2
IUPAC name
2-amino-6-(3-carboxypropanoylamino)heptanedioic acid
State
State

At room temperature, glutarylglutamic acid is a solid state compound. It is typically handled as a solid granule or powder.

Melting point (Celsius)
208.00
Melting point (Kelvin)
481.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
275.24g/mol
Molar mass
275.2370g/mol
Density
1.4600g/cm3
Appearence

Glutarylglutamic acid typically appears as a white crystalline powder. It is odorless and has a slightly acidic taste.

Comment on solubility

Solubility of 2-amino-6-(3-carboxypropanoylamino)heptanedioic acid

2-amino-6-(3-carboxypropanoylamino)heptanedioic acid, with the chemical formula C11H18N2O7, is an intriguing compound when it comes to solubility. Its structure, comprising multiple functional groups, strongly influences its behavior in various solvents.

The solubility characteristics of this compound can be summarized as follows:

  • Hydrophilic nature: The presence of multiple carboxyl groups (–COOH) enhances its affinity for water, generally leading to a greater solubility in polar solvents.
  • Amine group impact: The amino group (–NH2) further contributes to its solubility in aqueous solutions, as it can engage in hydrogen bonding with water molecules.
  • Temperature dependency: As with many organic compounds, solubility may increase with temperature, making it important to consider the conditions under which experiments are conducted.
  • pH Influence: The solubility can vary significantly depending on the pH of the surrounding environment due to the ionization of the carboxyl groups. In basic conditions, the compound may become more soluble.

In summary, one might say that "2-amino-6-(3-carboxypropanoylamino)heptanedioic acid displays a notable degree of solubility, particularly in polar solvents, owing to its rich array of functional groups." However, precise solubility information can best be determined through experimental data under specific conditions.

Interesting facts

Interesting Facts about 2-amino-6-(3-carboxypropanoylamino)heptanedioic acid

2-amino-6-(3-carboxypropanoylamino)heptanedioic acid, often referred to as a complex amino acid derivative, possesses remarkable structural features that make it an essential subject of study in biochemical research. Here are some intriguing aspects of this compound:

  • Amino Acid Connection: As an amino acid derivative, it plays a crucial role in protein synthesis and metabolic pathways.
  • Functional Groups: The presence of carboxyl (-COOH) groups in the structure enhances its reactivity, allowing it to participate in various biochemical reactions.
  • Potential Applications: This compound may have potential uses in medicinal chemistry and pharmaceuticals, especially regarding its effects on metabolic processes.
  • Biological Importance: Compounds with similar structures have been investigated for their roles in cellular signaling and metabolic regulation, highlighting the interconnectedness of amino acids in physiological functions.

To quote a leading researcher in the field, *“Understanding the complexities of amino acid derivatives opens up new avenues for therapeutic developments.”*
The exploration of this compound can provide insights into the intricate world of biochemistry, making it a significant addition to any chemist's repertoire.

Overall, the study of 2-amino-6-(3-carboxypropanoylamino)heptanedioic acid not only enriches our understanding of amino acids but also pushes the boundaries of research in areas like nutrition, drug design, and metabolic engineering.