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L-lysine monohydrochloride

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Identification
Molecular formula
C7H14N2O3
CAS number
59-22-7
IUPAC name
2-amino-6-formamido-hexanoic acid
State
State

At room temperature, this compound is typically found in a solid state, forming a stable crystalline powder that can be dissolved with specific solvents to aid in biochemical or pharmaceutical applications.

Melting point (Celsius)
263.00
Melting point (Kelvin)
536.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
146.19g/mol
Molar mass
146.1880g/mol
Density
1.2900g/cm3
Appearence

2-Amino-6-formamidohexanoic acid typically occurs as a white crystalline powder. Its structure and form hold significance in biochemical applications, especially in the field of nutrition and pharmaceuticals.

Comment on solubility

Solubility of 2-amino-6-formamido-hexanoic acid

2-amino-6-formamido-hexanoic acid, with the chemical formula C7H14N2O3, exhibits intriguing solubility characteristics due to its structural features. This compound possesses both amino and formamido functional groups, which plays a significant role in its solubility.

Key Aspects of Solubility:

  • Polarity: The presence of polar functional groups, such as –NH2 (amino group) and –CHO (formamido group), makes the compound generally soluble in polar solvents, particularly water.
  • Hydrogen Bonding: The ability of 2-amino-6-formamido-hexanoic acid to form hydrogen bonds with water molecules enhances its solubility, allowing for effective interaction in aqueous solutions.
  • Temperature Influence: Like many organic compounds, solubility may increase with temperature; thus, heating the solvent could potentially increase the dissolution rate.
  • Comparison with Similar Compounds: Compared to other amino acids or derivatives, this compound's unique structure likely leads to significant solubility, especially in physiological conditions.

In summary, the solubility of 2-amino-6-formamido-hexanoic acid can be characterized as favorable in polar solvents, largely due to its ionic and hydrogen-bonding capabilities. Understanding these solubility traits is important for potential applications in biochemical contexts.

Interesting facts

Interesting Facts about 2-Amino-6-formamido-hexanoic Acid

2-Amino-6-formamido-hexanoic acid is a fascinating compound belonging to the amino acid family, and it carries various intriguing properties that make it valuable in both scientific research and practical applications. Here are some notable aspects:

  • Amino Acid Derivative: This compound is an amino acid derivative, which means it has the fundamental structure of amino acids, including both an amine and a carboxylic acid functional group. This characteristic plays a crucial role in the formation of proteins.
  • Biological Significance: As a building block of proteins, this compound may have roles in various biological processes. Amino acids are essential for cellular function, contributing to enzyme activity, transport mechanisms, and overall metabolism.
  • Synthetic Applications: 2-Amino-6-formamido-hexanoic acid can be utilized in synthetic chemistry, particularly in the development of pharmaceuticals and biochemical substances. It holds potential for creating modified peptides or proteins that may exhibit enhanced activities.
  • Research Tool: Scientists often use amino acid derivatives like this compound to study protein folding, interactions, and enzymatic activities. The unique structure can lead to innovative findings in molecular biology and biochemistry.

As biochemist Dr. Jane Goodwin once said, "Amino acids are the building blocks of life; understanding them is key to unlocking the secrets of biology." This compound exemplifies that sentiment, showcasing the diversity and complexity inherent to amino acids.

Whether in a laboratory setting or as part of a broader biological research study, 2-amino-6-formamido-hexanoic acid certainly captures the curiosity and attention of those in the scientific community!

Synonyms
2-amino-6-formamidohexanoic acid
NSC-334317
NSC334317
N- epsilon -formyl-l-lysine
SCHEMBL9667036
2-amino-6-ormamidohexanoic acid
CHEBI:182422
DB-041439