Fmoc-D-Trp(Boc)-OH

97%

  • Product Code: 58017
  Alias:    Fmoc-D-
  CAS:    163619-04-3
Molecular Weight: 526.58 g./mol Molecular Formula: C₃₁H₃₀N₂O₆
EC Number: MDL Number: MFCD00153367
Melting Point: Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amine functionality, and the Boc (tert-butyloxycarbonyl) group protects the indole side chain of tryptophan. Its primary application is in the construction of peptide chains, ensuring selective deprotection and coupling steps during synthesis. It is especially valuable in synthesizing peptides containing tryptophan residues, as it prevents unwanted side reactions. The compound is commonly employed in pharmaceutical research, biotechnology, and the development of therapeutic peptides, where precise and controlled peptide assembly is critical. Its stability and compatibility with SPPS protocols make it a reliable choice for producing complex peptides with high purity.
Product Specification:
Test Specification
PURITYHPLC 97 100%
SPECIFIC ROTATION A20DC1 DMF 16.5 21.5
APPEARANCE WHITE TO LIGHT YELLOW POWDER
ELEMENTAL ANALYSIS CONSISTENT
PROTON NMR SPECTRUM Conforms to Structure
TLC ANALYSIS ONE SPOT
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿500.00
+
-
5.000 10-20 days ฿2,440.00
+
-
25.000 10-20 days ฿11,700.00
+
-
Fmoc-D-Trp(Boc)-OH
This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amine functionality, and the Boc (tert-butyloxycarbonyl) group protects the indole side chain of tryptophan. Its primary application is in the construction of peptide chains, ensuring selective deprotection and coupling steps during synthesis. It is especially valuable in synthesizing peptides containing tryptophan residues, as it prevents unwanted side reactions. The compound is commonly employed in pharmaceutical research, biotechnology, and the development of therapeutic peptides, where precise and controlled peptide assembly is critical. Its stability and compatibility with SPPS protocols make it a reliable choice for producing complex peptides with high purity.
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