45234-02-4

Basic information

• Product Name: H-LYS-GLU-OH
• Synonyms: H-LYS-GLU-OH;H-GLU-EPSILON-LYS-OH;L-LYS-L-GLU;L-LYSYL-L-GLUTAMIC ACID;L-LysyI-L-glutamate;L-Lys-L-Glu-OH;Lys-Glu-OH;N-L-Lysyl-L-glutamic acid
• CAS NO: 45234-02-4
• Molecular Formula: C₁₁H₂₁N₃O₅
• Molecular Weight: 275.3
• Mol File: 45234-02-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 195-197 °C
• Boiling Point: 596.4 °C at 760 mmHg
• Flash Point: 314.5 °C
• Appearance: /
• Density: 1.29 g/cm³
• Storage Temp.: -15°C
• PKA: 3.00±0.10(Predicted)
• CAS DataBase Reference: H-LYS-GLU-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-LYS-GLU-OH(45234-02-4)
• EPA Substance Registry System: H-LYS-GLU-OH(45234-02-4)

Safety Data

• Hazardous Substances Data: 45234-02-4(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Definition

ChEBI: A dipeptide formed from L-lysine and L-glutamic acid residues.

Upstream product

• 56-86-0 L-glutamic acid 
• 657-27-2 L-Lysine hydrochloride 

Downstream Products

• 290-37-9 1,4-pyrazine 
• 109-08-0 2-Methylpyrazine 
• 123-32-0 2,5-dimethyl-pyrazine 
• 5910-89-4 2,3-dimethylpyrazine 
• 13360-65-1 2-ethyl-3,6-dimethylpyrazine 
• 108-50-9 2,6-dimethylpyrazine 
• 14667-55-1 2,3,5-trimethylpyrazine 
• 13925-07-0 2-ethyl-3,5-dimethylpyrazine 
• 13360-64-0 2-ethyl-5-methypyrazine 
• 15707-34-3 5-ethyl-2,3-dimethylpyrazine 
• 80935-98-4 3-ethenyl-2,5-dimethylpyrazine 
• 22047-27-4 1-(5-methylpyrazin-2-yl)ethanone 
• 18433-97-1 2,5-dimethyl-3-propylpyrazine 

Relevant articles and documents

Modelling of prebiotic synthesis and selection of peptides under isothermal conditions and thermal cycling mode

The model peptide synthesis from mixtures of amino acids was carried out under the thermal cycling and isothermal modes. The compositions of the obtained mixtures of products and the primary amino acid sequence of the synthesized peptides were determined by Fourier transform ion cyclotron resonance mass spectrometry and tandem mass spectrometry in combination with high-performance liquid chromatography with the application of de novo sequencing of the synthesized products. The processes of abiogenous synthesis of peptides were shown to occur under relatively mild temperature conditions and give a substantially less number of peptides as compared with the possible statistical set. The evolution of the system takes place in the process of the synthesis in solid phase with the disappearance of a series of the most unstable peptides. The selection process with the formation of complementary peptides takes place in peptide synthesis under the thermal cyclic mode.