Nε-Carbobenzoxy-L-lysine

98%

  • Product Code: 59207
  Alias:    N6-Cbz-L-Lysine; N6-Benzyloxycarbonyl-L-Lysine
  CAS:    1155-64-2
Molecular Weight: 280.32 g./mol Molecular Formula: C₁₄H₂₀N₂O₄
EC Number: 214-585-7 MDL Number: MFCD00002638
Melting Point: 259 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: Room temperature, dry, sealed
Product Description: Nε-Carbobenzoxy-L-lysine is widely used in peptide synthesis as a protecting group for the ε-amino group of lysine. This protection is crucial during the synthesis process to prevent unwanted side reactions and ensure the correct sequence of amino acids in the peptide chain. Once the peptide synthesis is complete, the Nε-Carbobenzoxy group can be selectively removed without affecting other functional groups in the molecule. This chemical is particularly valuable in the production of complex peptides and proteins, where precise control over the reaction conditions is essential. Additionally, it finds applications in the development of pharmaceuticals, including the synthesis of peptide-based drugs and bioactive compounds. Its role in facilitating the efficient and accurate assembly of peptides makes it a key reagent in both research and industrial settings.
Product Specification:
Test Specification
PURITYNONAQUEOUS TITRATION 97.5 102.5%
HCL 14.5-16.5
APPEARANCE WHITE TO LIGHT YELLOW POWDER
CLAARITY OF SOLUTION 0.3 GRAM IN 2ML TFA CLEAR SOLUTION
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿300.00
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25.000 10-20 days ฿700.00
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100.000 10-20 days ฿2,620.00
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Nε-Carbobenzoxy-L-lysine
Nε-Carbobenzoxy-L-lysine is widely used in peptide synthesis as a protecting group for the ε-amino group of lysine. This protection is crucial during the synthesis process to prevent unwanted side reactions and ensure the correct sequence of amino acids in the peptide chain. Once the peptide synthesis is complete, the Nε-Carbobenzoxy group can be selectively removed without affecting other functional groups in the molecule. This chemical is particularly valuable in the production of complex peptides and proteins, where precise control over the reaction conditions is essential. Additionally, it finds applications in the development of pharmaceuticals, including the synthesis of peptide-based drugs and bioactive compounds. Its role in facilitating the efficient and accurate assembly of peptides makes it a key reagent in both research and industrial settings.
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