4337-37-5

Basic information

• Product Name: DL-LEUCYL-GLYCYL-GLYCINE
• Synonyms: H-DL-LEU-GLY-GLY-OH;DL-LEUCYL-GLYCYL-GLYCINE;DL-LEU-GLY-GLY;N-(N-DL-leucylglycyl)glycine;GL-Leucyl-glycyl-glycine;EINECS 224-384-6;(±)-N-(N-Leucylglycyl)glycine;2-[[2-[(2-amino-4-methylpentanoyl)amino]acetyl]amino]acetic acid
• CAS NO: 4337-37-5
• Molecular Formula: C₁₀H₁₉N₃O₄
• Molecular Weight: 245.28
• EINECS: 224-384-6
• Product Categories: Biochemistry;Oligopeptides;Peptide Synthesis;Dipeptides and Tripeptides;Peptides;Tripeptides
• Mol File: 4337-37-5.mol

Chemical Properties

• Melting Point: >240℃ (water ethanol )
• Boiling Point: 573.7 °C at 760 mmHg
• Flash Point: 300.8 °C
• Appearance: /
• Density: 1.28 g/cm3
• Storage Temp.: −20°C
• PKA: 3.30±0.10(Predicted)
• CAS DataBase Reference: DL-LEUCYL-GLYCYL-GLYCINE(CAS DataBase Reference)
• NIST Chemistry Reference: DL-LEUCYL-GLYCYL-GLYCINE(4337-37-5)
• EPA Substance Registry System: DL-LEUCYL-GLYCYL-GLYCINE(4337-37-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 4337-37-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
DL-Leucyl-Glycyl-Glycine is used as a model compound for understanding the behavior and properties of peptides, which aids in the development of new drugs and therapeutic agents.
Used in Drug Delivery Systems:
DL-Leucyl-Glycyl-Glycine is used as a component in drug delivery systems to enhance the efficacy and targeted delivery of pharmaceuticals.
Used in Peptide Development:
DL-Leucyl-Glycyl-Glycine is used as a building block for the synthesis of new peptides with specific therapeutic or industrial applications.
Used in Antioxidant and Anti-Inflammatory Research:
DL-Leucyl-Glycyl-Glycine is studied for its potential antioxidant and anti-inflammatory properties, making it a candidate for further investigation in medical research and development.
Used in Chemical Research:
DL-Leucyl-Glycyl-Glycine is used as a synthetic peptide in chemical research to explore its interactions with other molecules and its potential applications in various chemical processes.

InChI:InChI=1/C10H19N3O4/c1-6(2)3-7(11)10(17)13-4-8(14)12-5-9(15)16/h6-7H,3-5,11H2,1-2H3,(H,12,14)(H,13,17)(H,15,16)

Upstream product

• 94230-81-6 N-[N-(DL-2-bromo-4-methyl-valeryl)-glycyl]-glycine 
• 94230-81-6 N-[N-(D-2-bromo-4-methyl-valeryl)-glycyl]-glycine 
• 59685-29-9 glycyl=>leucyl=>glycine 
• 28659-88-3 (R)-2-Bromo-4-methyl-pentanoyl chloride 
• 100348-21-8 Leu-Gly-Gly-OEt 
• 627-74-7 glycylglycine ethyl ester 
• 3190-70-3 L-leucine N-carboxyanhydride 
• 61-90-5 L-leucine 
• 51021-87-5 N-benzyloxycarbonyl-L-leucine methyl ester 
• 20806-85-3 N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycine ethyl ester 
• 76863-45-1 (S)-benzyl (1-azido-4-methyl-1-oxopentan-2-yl)carbamate 
• 4703-53-1 N-benzyloxycarbonyl-L-leucine hydrazide 
• 14297-22-4 N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycine 

Downstream Products

• 61-90-5 L-leucine 
• 556-50-3 glycylglycine 
• 56-40-6 glycine 
• 157240-56-7 3-isobutyl-piperazine-2,5-dione 
• 615-82-7 DL-Leucyl-glycin 
• 688-14-2 glycylleucine 
• 59685-29-9 glycyl=>leucyl=>glycine 
• 2010-15-3 3-phenyl-2-thioxoimidazolidin-4-one 
• 4399-40-0 5-isobutyl-3-phenyl-2-thioxo-imidazolidin-4-one 
• 328-39-2 LEUCINE 
• 686-50-0 L-leucyl-glycine 
• 141-43-5 ethanolamine 
• 7325-21-5 glycyl=>leucyl=>glycyl=>glycine 

Relevant articles and documents

Peptide Decomposition in the Neutral pH Region via the Formation of Diketopiperazines

In the neutral pH region, the decomposition of the tripeptides Leu-Gly-Gly and Gly-Leu-Gly at 130 deg C and the hexapeptide Phe-Gly-Leu-Gly-Val-Gly at 100 deg C has been found to involve the formation of diketopiperazines from the N-terminal position of the peptides.