N-Carbobenzyloxy-L-leucine

90%

  • Product Code: 105552
  Alias:    N-Benzyloxycarbonyl-L-leucine; N-carboxy-L-leucine, CBZ-L-leucine
  CAS:    2018-66-8
Molecular Weight: 265.3 g./mol Molecular Formula: C₁₄H₁₉NO₄
EC Number: 217-960-3 MDL Number: MFCD00026494
Melting Point: Boiling Point:
Density: 1 g/mL at 25 °C(lit.) Storage Condition: 2-8°C
Product Description: N-Carbobenzyloxy-L-leucine is primarily used in peptide synthesis as a protecting group for the amino group of leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds accurately. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of amino acids are crucial. Additionally, it finds applications in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where precise control over molecular structure is essential for efficacy and safety. Its role in organic synthesis also extends to the preparation of intermediates for various bioactive compounds.
Product Specification:
Test Specification
Appearance Colorless To Pale Yellow Viscous Liquid
Purity (%) 89.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $13.29
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25.000 10-20 days $45.27
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100.000 10-20 days $107.98
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N-Carbobenzyloxy-L-leucine
N-Carbobenzyloxy-L-leucine is primarily used in peptide synthesis as a protecting group for the amino group of leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds accurately. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of amino acids are crucial. Additionally, it finds applications in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where precise control over molecular structure is essential for efficacy and safety. Its role in organic synthesis also extends to the preparation of intermediates for various bioactive compounds.
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