Nε-Trifluoroacetyl-L-lysine

97%

  • Product Code: 59210
  Alias:    N6-Trifluoroacetyl-L-lysine; Trifluoroacetyllysine, ε-TFA-lysine
  CAS:    10009-20-8
Molecular Weight: 242.2 g./mol Molecular Formula: C₈H₁₃F₃N₂O₃
EC Number: MDL Number: MFCD00037223
Melting Point: 258 Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Nε-Trifluoroacetyl-L-lysine is widely used in peptide synthesis as a protecting group for the ε-amino group of lysine. This modification prevents unwanted side reactions during the formation of peptide bonds, ensuring the synthesis proceeds smoothly and efficiently. It is particularly valuable in solid-phase peptide synthesis, where selective protection and deprotection are crucial for building complex peptide sequences. Additionally, it finds applications in biochemical research, where it aids in the study of protein structure and function by allowing precise modifications to lysine residues. Its stability under various reaction conditions makes it a reliable choice for advanced chemical and biological studies.
Product Specification:
Test Specification
PURITYHPLC 97 100%
HCL 17-20
WATER BY KARL FISCHER 0 6%
APPEARANCE White to off-white powder
PROTON NMR SPECTRUM Conforms to Structure
SOLUBILITY IN 2M HCL COLORLESS CLEAR (< 3.5 NTU) ,10 MG/ML
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿350.00
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25.000 10-20 days ฿1,120.00
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100.000 10-20 days ฿4,080.00
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-
500.000 10-20 days ฿13,440.00
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Nε-Trifluoroacetyl-L-lysine
Nε-Trifluoroacetyl-L-lysine is widely used in peptide synthesis as a protecting group for the ε-amino group of lysine. This modification prevents unwanted side reactions during the formation of peptide bonds, ensuring the synthesis proceeds smoothly and efficiently. It is particularly valuable in solid-phase peptide synthesis, where selective protection and deprotection are crucial for building complex peptide sequences. Additionally, it finds applications in biochemical research, where it aids in the study of protein structure and function by allowing precise modifications to lysine residues. Its stability under various reaction conditions makes it a reliable choice for advanced chemical and biological studies.
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