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Atomfair N2-(1-Oxododecyl)-L-lysine C18H36N2O3

Description N2-(1-Oxododecyl)-L-lysine (CAS No. 52315-75-0) is a high-purity lysine derivative with the molecular formula C18H36N2O3. This compound, also known by its IUPAC name 6-amino-2-(dodecanoylamino)hexanoic acid , is a modified amino acid featuring a lauroyl (C12) fatty acid chain. It is widely utilized in biochemical research, particularly in studies involving lipidated peptides, protein modifications, and surfactant applications. The product is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for sensitive experimental workflows. Its amphiphilic nature makes it valuable for membrane interaction studies and as a building block for advanced biomaterials. Store at 2-8??C in a…

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Description

Description

N2-(1-Oxododecyl)-L-lysine (CAS No. 52315-75-0) is a high-purity lysine derivative with the molecular formula C18H36N2O3. This compound, also known by its IUPAC name 6-amino-2-(dodecanoylamino)hexanoic acid, is a modified amino acid featuring a lauroyl (C12) fatty acid chain. It is widely utilized in biochemical research, particularly in studies involving lipidated peptides, protein modifications, and surfactant applications. The product is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for sensitive experimental workflows. Its amphiphilic nature makes it valuable for membrane interaction studies and as a building block for advanced biomaterials. Store at 2-8??C in a tightly sealed container to maintain stability.

  • CAS No: 52315-75-0
  • Molecular Formula: C18H36N2O3
  • Molecular Weight: 328.5
  • Exact Mass: 328.27259301
  • Monoisotopic Mass: 328.27259301
  • IUPAC Name: 6-amino-2-(dodecanoylamino)hexanoic acid
  • SMILES: CCCCCCCCCCCC(=O)NC(CCCCN)C(=O)O
  • Synonyms: N2-(1-Oxododecyl)-L-lysine, N-Lauroyl-DL-lysine, 6-amino-2-(dodecanoylamino)hexanoic acid, 186832-69-9, N6-Lauroyl-L-lysine;

Application

N2-(1-Oxododecyl)-L-lysine is employed in peptide synthesis to introduce hydrophobic modifications, enhancing membrane permeability. Researchers use it to study lipid-protein interactions and as a surfactant in nanoparticle formulations. Its amphiphilic properties also make it suitable for investigating self-assembling biomaterials and drug delivery systems.

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