Glutamyllysine | Solubility of Things

Identification

Molecular formula

C₁₁H₂₁N₃O₆

CAS number

84300-93-4

IUPAC name

2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid

State

At room temperature, Glutamyllysine is typically a solid. It is stable under normal conditions and does not evaporate or sublimate at standard temperatures and pressures.

Melting point (Celsius)

265.00

Melting point (Kelvin)

538.00

Boiling point (Celsius)

244.00

Boiling point (Kelvin)

517.00

General information

Molecular weight

275.31g/mol

Molar mass

275.3080g/mol

Density

1.4600g/cm³

Appearence

2-Amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid, more commonly known as Glutamyllysine, typically appears as a white or off-white crystalline solid. It is often found as a powder and is generally odorless.

Comment on solubility

Solubility of 2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid

The solubility of 2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid, with the chemical formula C₁₁H₂₁N₃O₆, is particularly noteworthy due to its unique chemical structure. As an amino acid derivative, this compound exhibits a range of solubility behaviors that can be influenced by various factors.

Key Factors Affecting Solubility:

pH Levels: The solubility of amino acids is often pH-dependent, due to the presence of ionizable functional groups. In acidic or neutral solutions, this compound is likely to be more soluble.
Temperature: Increased temperature generally enhances solubility, making warm solutions more effective for dissolving this compound compared to cold solutions.
Solvent Properties: Polar solvents such as water will typically facilitate greater solubility for this compound due to its hydrophilic amino and carboxyl groups.

Moreover, it's important to note that the presence of multiple amine and carboxyl functional groups can contribute to a complex solubility profile, allowing it to interact favorably with numerous solvents. In comparison to simpler organic compounds, 2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid may present unique challenges or advantages when attempting to dissolve it in various media.

In conclusion, while this compound possesses a potential for good solubility in appropriate conditions, specific experimental evaluations are recommended to determine detailed solubility characteristics in practice. Understanding these aspects can significantly influence its application in chemical and biopharmaceutical contexts.

Interesting facts

Interesting Facts about 2-Amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic Acid

2-Amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid is a fascinating compound that belongs to the class of amino acids, and its complex structure reflects its unique properties and potential applications. Here are some noteworthy points:

Structural Complexity: The compound features multiple functional groups including amine and carboxylic acids which contribute to its reactivity and ability to form various derivatives.
Biological Significance: As an amino acid derivative, this compound is vital in biochemical processes and could play a role in protein synthesis.
Potential Therapeutic Applications: Research suggests that compounds with similar structures may have implications in therapeutic areas such as cancer treatment and metabolic disorders.
Research Interest: Its structural diversity has made it the subject of numerous studies, focusing on its interactions at the molecular level, which can contribute to advances in medicinal chemistry.
Synthetic Challenges: The synthesis of such intricate compounds often presents unique challenges, requiring innovative synthetic pathways to achieve the desired chemical structures.

In conclusion, 2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxy-butanoyl]amino]heptanedioic acid serves as an excellent example of how complex organic molecules can have profound implications in science and medicine. As the field of chemistry progresses, compounds like this open doors for understanding biological systems and developing new treatments.

Synonyms

CHEBI:177656

Alanyl-N-(5-amino-1,5-dicarboxypentyl)glutamine

2-amino-6-[[4-(2-aminopropanoylamino)-4-carboxybutanoyl]amino]heptanedioic acid