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Lysinoalanine

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Identification
Molecular formula
C8H16N3O2
CAS number
1973-82-2
IUPAC name
2-amino-6-(1-aminoethylideneamino)hexanoic acid
State
State

At room temperature, lysinoalanine is typically a solid. It is often found in trace amounts as an artifact from protein processing in food industry and laboratory preparations.

Melting point (Celsius)
225.00
Melting point (Kelvin)
498.15
Boiling point (Celsius)
100.00
Boiling point (Kelvin)
373.15
General information
Molecular weight
172.24g/mol
Molar mass
172.2420g/mol
Density
1.2900g/cm3
Appearence

Lysinoalanine typically appears as a crystalline solid, although the exact characteristics can vary depending on its form and purity. It is not usually encountered in a pure state under normal conditions as it tends to occur as part of hydrolyzed protein materials.

Comment on solubility

Solubility of 2-amino-6-(1-aminoethylideneamino)hexanoic acid

2-amino-6-(1-aminoethylideneamino)hexanoic acid, with the chemical formula C8H16N3O2, exhibits interesting solubility characteristics primarily due to the presence of multiple amino groups in its structure. These groups facilitate hydrogen bonding with water molecules, significantly impacting its solubility profile.

Key points regarding its solubility are:

  • Solubility in Water: Generally, compounds with amino and carboxylic acid functional groups tend to be soluble in water because they can form interactions with polar solvents.
  • pH Dependence: The solubility may vary based on the pH of the solution, given that amino acids can exist in charged forms at different pH levels.
  • Temperature Effects: As with many organic compounds, increased temperature may enhance solubility, making it more versatile in various applications.

As a general rule, “like dissolves like.” Hence, 2-amino-6-(1-aminoethylideneamino)hexanoic acid’s polar nature indicates that it is more likely to be soluble in polar solvents compared to non-polar solvents. However, conducting empirical solubility tests would provide precise data for practical applications.

Interesting facts

Interesting Facts About 2-amino-6-(1-aminoethylideneamino)hexanoic Acid

2-amino-6-(1-aminoethylideneamino)hexanoic acid, commonly referred to by its systematic name, is a fascinating compound in the field of biochemistry and pharmaceuticals. Here are some intriguing aspects of this amino acid derivative:

  • Peptide Building Block: This compound serves as a vital building block in the synthesis of peptides, specifically in the formation of complex proteins that play essential roles in biological systems.
  • Resemblance to Naturally Occurring Amino Acids: Its structural characteristics resemble those of naturally occurring amino acids, making it a significant point of interest for synthetic biologists and medicinal chemists alike.
  • Potential Applications: Research suggests this compound could have applications in drug design, particularly as a scaffold for new therapeutic agents due to its unique functional groups.
  • Research Interest: Scientists are keenly studying its properties to explore connections with metabolic pathways and protein interactions, which opens avenues for understanding physiological mechanisms.
  • Anticipated Role in Enzyme Function: The presence of amine groups indicates potential participation in enzymatic reactions, influencing the rate and mechanisms by which enzymes catalyze biological processes.

In a world where compounds like 2-amino-6-(1-aminoethylideneamino)hexanoic acid bridge the gap between simple amino acids and complex biomolecules, researchers are reminded of the intricate web of interactions that govern life at the molecular level. As one scientist noted, "Understanding these small molecules is key to unlocking the secrets of more extensive biological systems."

With ongoing research, we can expect more exciting discoveries concerning this compound, highlighting its essential role in the broader context of chemistry and biology.

Synonyms
53774-63-3
2-amino-6-(1-aminoethylideneamino)hexanoic acid
H-Lys(acetimidoyl)-OH
6-Acetimidamido-2-aminohexanoic acid
N-(5-amino-5-carboxypentyl)acetamidine
2-AMINO-6-[(1-AMINOETHYLIDENE)AMINO]HEXANOIC ACID
L-NIL;H-Lys(1-iminoethyl)-OH;N-(5-Amino-5-carboxypentyl)-acetamidine
Ne-Acetimidoyl-L-lysine
N~6~-Ethanimidoyllysine
SCHEMBL934874
SCHEMBL26908936
DTXSID30861424
ONYFNWIHJBLQKE-UHFFFAOYSA-N
HMS3746E17
HSCI1_000308
FL107911