Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
03802
CAS Number:
16965-06-3
N-Boc-N-trifluoroacetyl-L-lysine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Lys(Tfa)-OH
Documents
$29.34 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Na-Boc-Ne-trifluoroacetyl-L-lysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its protective Boc (tert-butyloxycarbonyl) and trifluoroacetyl groups, which enhance the stability and reactivity of the lysine residue during chemical reactions. Researchers utilize Na-Boc-Ne-trifluoroacetyl-L-lysine in the synthesis of complex peptides and proteins, enabling the incorporation of lysine into various sequences while maintaining the integrity of the amino acid. Its unique structure allows for selective modifications, making it an essential building block in the development of pharmaceuticals, particularly in the fields of biochemistry and medicinal chemistry.

In addition to its applications in peptide synthesis, Na-Boc-Ne-trifluoroacetyl-L-lysine is also utilized in the study of protein interactions and enzyme activity, providing insights into biological processes. Its ability to facilitate the introduction of functional groups makes it a valuable tool for researchers aiming to explore new therapeutic avenues. The compound's stability and ease of use compared to similar derivatives further enhance its appeal in laboratory settings, ensuring reliable results in various applications.

Synonyms
Boc-L-Lys(Tfa)-OH
CAS Number
16965-06-3
Purity
≥ 99% (HPLC)
Molecular Formula
C13H21F3N2O5
Molecular Weight
342.3
MDL Number
MFCD00037104
PubChem ID
295485
Appearance
White powder
Optical Rotation
[a]D20 = -11 ± 1º (C=2 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Lys(Tfa)-OH
CAS Number
16965-06-3
Purity
≥ 99% (HPLC)
Molecular Formula
C13H21F3N2O5
Molecular Weight
342.3
MDL Number
MFCD00037104
PubChem ID
295485
Appearance
White powder
Optical Rotation
[a]D20 = -11 ± 1º (C=2 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Ne-trifluoroacetyl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing chemists to create complex structures with enhanced stability and reactivity.
  • Drug Development: It plays a significant role in medicinal chemistry, particularly in the design of new pharmaceuticals targeting specific biological pathways, thanks to its unique functional groups.
  • Bioconjugation: The trifluoroacetyl group enables selective reactions with biomolecules, making it useful for creating bioconjugates that can be employed in targeted drug delivery systems.
  • Research in Protein Engineering: This compound is essential in modifying lysine residues in proteins, facilitating studies on protein function and interaction, which is crucial for understanding disease mechanisms.
  • Analytical Chemistry: It can be utilized as a standard in mass spectrometry, aiding in the identification and quantification of similar compounds in complex mixtures.

Citations