H-DL-Nle-OH

98%

  • Product Code: 104935
  Alias:    DL-norleucine ; 2-aminocaproic acid
  CAS:    616-06-8
Molecular Weight: 131.17 g./mol Molecular Formula: C₆H₁₃NO₂
EC Number: 210-462-7 MDL Number: MFCD00064422
Melting Point: >300 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is commonly used in peptide synthesis as a building block for creating modified peptides. It serves as a non-natural amino acid analog, allowing researchers to study peptide structure and function by replacing natural amino acids like leucine or methionine. Its application is particularly valuable in the development of peptide-based drugs, where it can enhance stability, bioavailability, or resistance to enzymatic degradation. Additionally, it is utilized in biochemical research to investigate protein-protein interactions and folding mechanisms. Its incorporation into peptides can also aid in the study of receptor binding and signal transduction pathways.
Product Specification:
Test Specification
Chloride (Cl) 0-0.02
Purity (Gc) 98-100
Specific Rotation [A]20/D(C=1, 5Mol/L Hcl) 0.5
Specific Rotation [A]20/D(C=1, 5Mol/L Hcl)
Appearance White To Off-White Powder
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $32.25
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25.000 10-20 days $103.03
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100.000 10-20 days $298.88
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H-DL-Nle-OH
This compound is commonly used in peptide synthesis as a building block for creating modified peptides. It serves as a non-natural amino acid analog, allowing researchers to study peptide structure and function by replacing natural amino acids like leucine or methionine. Its application is particularly valuable in the development of peptide-based drugs, where it can enhance stability, bioavailability, or resistance to enzymatic degradation. Additionally, it is utilized in biochemical research to investigate protein-protein interactions and folding mechanisms. Its incorporation into peptides can also aid in the study of receptor binding and signal transduction pathways.
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