Fmoc-Phe-OH

98%

  • Product Code: 105108
  Alias:    Fmoc-L-phenylalanine ; N-fluorenylmethoxycarbonyl-L-phenylalanine
  CAS:    35661-40-6
Molecular Weight: 387.43 g./mol Molecular Formula: C₂₄H₂₁NO₄
EC Number: 252-661-1 MDL Number: MFCD00037128
Melting Point: 180-187 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Fmoc-Phe-OH is widely used in peptide synthesis as a building block. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the Fmoc (fluorenylmethyloxycarbonyl) protecting group, which can be easily removed under mild basic conditions without affecting the peptide chain. This compound is essential for introducing phenylalanine residues into peptides, which are crucial for the structure and function of many bioactive peptides and proteins. Its application extends to the development of pharmaceuticals, research in biochemistry, and the production of custom peptides for therapeutic and diagnostic purposes. The stability and efficiency of Fmoc-Phe-OH make it a preferred choice in modern peptide chemistry.
Product Specification:
Test Specification
Purity (%) 98-100
Melting Point 180-187
Appearance White Powder Or Crystals
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $11.40
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25.000 10-20 days $35.70
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100.000 10-20 days $112.51
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Fmoc-Phe-OH
Fmoc-Phe-OH is widely used in peptide synthesis as a building block. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the Fmoc (fluorenylmethyloxycarbonyl) protecting group, which can be easily removed under mild basic conditions without affecting the peptide chain. This compound is essential for introducing phenylalanine residues into peptides, which are crucial for the structure and function of many bioactive peptides and proteins. Its application extends to the development of pharmaceuticals, research in biochemistry, and the production of custom peptides for therapeutic and diagnostic purposes. The stability and efficiency of Fmoc-Phe-OH make it a preferred choice in modern peptide chemistry.
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