Trilysine

CAS Number13184-14-0
Molecular FormulaC18H38N6O4
Molecular Weight402.5
InChI KeyWBSCNDJQPKSPII-KKUMJFAQSA-N
LogP-5.6
Synonyms
  • Lysyllysyllysine
  • Lys-Lys-Lys
  • 13184-14-0
  • Trilysine
  • l-lysyl-l-lysyl-l-lysine
  • L-Lysine, L-lysyl-L-lysyl-
  • lysyl-lysyl-lysine
  • (S)-6-Amino-2-((S)-6-amino-2-((S)-2,6-diaminohexanamido)hexanamido)hexanoic acid
  • H-Lys-Lys-Lys-OH Acetate Salt
  • Y7F82M80K8
  • (2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-2,6-diaminohexanoyl]amino]hexanoyl]amino]hexanoic acid
  • UNII-Y7F82M80K8
  • 2olb
  • L-Lysine,L-lysyl-L-lysyl-
  • SCHEMBL3796535
  • CHEMBL1229077
  • DTXSID40948891
  • CHEBI:160118
  • AKOS027320373
  • CS-W009720

Applications:

HPLC Method for Separation of  Lysine, Dilysine and Trilysine on BIST B+ Column

March 27, 2024

High Performance Liquid Chromatography (HPLC) Method for Analysis of Lysine, Dilysine, Trilysine on BIST B+ by SIELC Technologies

Separation type: Bridge Ion Separation Technology, or BIST™ by SIELC Technologies

HPLC Method for Analysis of Lysine, Dilysine, Trilysine on on BIST B+ by SIELC Technologies

Lysine, dilysine, and trilysine refer to compounds related to the amino acid lysine.

1. Lysine (L-Lysine):

  • Type: Lysine is an essential amino acid.
  • Structure: It has an α-amino group (which is in the protonated –NH3+ form under biological conditions), an α-carboxylic acid group (which is in the deprotonated –COO− form under physiological conditions), and a side chain with a functional group that is a basic, charged (at physiological pH) amino group.
  • Role in the Body: As an amino acid, lysine is a building block for proteins. It’s crucial for health, but the body can’t produce it, so it must come from the diet.
  • Uses: Lysine has been used in supplements to improve athletic performance, support immune health, and more. It’s also integral in the production of carnitine, a nutrient responsible for converting fatty acids into energy and helping to lower cholesterol.

2. Dilysine:

  • Type: This refers to a molecule composed of two lysine units.
  • Structure: The two lysine amino acids can be joined via a peptide bond between the carboxyl group of one lysine molecule and the amino group of another, forming a dipeptide. The resulting structure still features the basic side chains of the lysine residues.
  • Potential Roles and Uses: While not commonly discussed outside of scientific research, such compounds could play roles in biological signaling or act as building blocks for more complex molecules. They may also be used in certain types of biochemical research or have potential therapeutic properties.

3. Trilysine:

  • Type: This compound comprises three lysine molecules.
  • Structure: Similar to dilysine, but with three lysine units connected by peptide bonds, resulting in a tripeptide. The basic side chains characteristic of lysine would still be present, and the molecule would carry multiple positive charges under physiological conditions due to these groups.
  • Potential Roles and Uses: Trilysine is even less common in general discussion and is primarily a subject of scientific study. It could play a role in biochemical research or be explored for various potential applications, perhaps related to its charge and interaction with other molecules.

For all these compounds, especially dilysine and trilysine, their relevance is often in biochemical research. Scientists may study such peptides to understand cellular mechanisms, explore physiological processes, or develop new materials or medications. The specific properties of these compounds, such as their charge and their ability to participate in various biochemical interactions, can make them valuable for certain applications.

Lysine, dilysine, and trilysine can be retained, separated and analyzed on a BIST B+ mixed-mode stationary phase column using an analytical method with a simple mobile phase of water, Acetonitrile (MeCN) or Methanol (MeOH), and a sulfuric acid as a buffer. This analysis method can be detected using UV at 205 nm.

High Performance Liquid Chromatography (HPLC) Method for Analyses of Lysine, Dilysine, Trilysine

Condition

ColumnBIST B+, 4.6 x 50 mm, 5 µm, 100 A
Mobile PhaseGradient MeCN or MeOH
Buffer H2SO4 -0.2%
Flow Rate1.0 ml/min
DetectionUV 205 nm

Description

Class of CompoundsAmino acid
Analyzing CompoundsLysine, Dilysine, Trilysine

Application Column

BIST B+

Column Diameter: 4.6 mm
Column Length: 50 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Dilysine
Lysine
Trilysine
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.