Boc-4-Amino-L-phenylalanine

98%

  • Product Code: 104665
  Alias:    BOC-4-amino-L-phenylalanine ;N-tert-butoxycarbonyl-4-amino-L-phenylalanine,N-tert-butoxycarbonyl-4-amino-L-phenylalanine
  CAS:    55533-24-9
Molecular Weight: 280.32 g./mol Molecular Formula: C₁₄H₂₀N₂O₄
EC Number: MDL Number: MFCD00038139
Melting Point: Boiling Point:
Density: Storage Condition: -20°C
Product Description: Boc-4-Amino-L-phenylalanine is widely used in peptide synthesis as a protected amino acid. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the controlled and sequential addition of amino acids to build complex peptides. After the peptide chain is assembled, the Boc group can be selectively removed under mild acidic conditions, revealing the free amino group for further reactions. Additionally, it is employed in the synthesis of modified peptides and peptidomimetics, where precise control over amino acid incorporation is essential. Its application extends to the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology.
Product Specification:
Test Specification
Melting Point 125-131
Purity (HPLC) 98-100
Specific Rotation 23-29
Appearance White To Pale Yellow Powder
Infrared Spectrum Conforms To Structure
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $24.38
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5.000 10-20 days $88.09
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25.000 10-20 days $387.75
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Boc-4-Amino-L-phenylalanine
Boc-4-Amino-L-phenylalanine is widely used in peptide synthesis as a protected amino acid. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the controlled and sequential addition of amino acids to build complex peptides. After the peptide chain is assembled, the Boc group can be selectively removed under mild acidic conditions, revealing the free amino group for further reactions. Additionally, it is employed in the synthesis of modified peptides and peptidomimetics, where precise control over amino acid incorporation is essential. Its application extends to the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology.
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