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Catalog Number:
05506
CAS Number:
96561-04-5
N-Boc-N-trifluoroacetyl-D-lysine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-Lys(Tfa)-OH
Documents
$81.92 /250MG
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Product Information

Na-Boc-Ne-trifluoroacetyl-D-lysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and usability in various chemical reactions. The trifluoroacetyl group adds unique properties, making it particularly valuable in the synthesis of peptide-based therapeutics and in the study of protein interactions. Researchers appreciate its ability to facilitate the selective modification of lysine residues, which is essential in the design of biologically active compounds.

In practical applications, Na-Boc-Ne-trifluoroacetyl-D-lysine is utilized in the pharmaceutical industry for the development of novel peptides and as a building block in the synthesis of complex biomolecules. Its unique structure allows for improved solubility and bioavailability, making it an attractive option for drug formulation. Additionally, its role in enhancing the stability of peptides under physiological conditions opens up new avenues for research in drug delivery systems and targeted therapies. This compound is an essential tool for researchers aiming to innovate in the fields of medicinal chemistry and biochemistry.

Synonyms
Boc-D-Lys(Tfa)-OH
CAS Number
96561-04-5
Purity
≥ 98% (HPLC)
Molecular Formula
C13H21F3N2O5
Molecular Weight
342.3
MDL Number
MFCD00236857
PubChem ID
295485
Melting Point
103-109 °C
Optical Rotation
[a]D22 = +3 ± 2º (C=1 in Acetone)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Lys(Tfa)-OH
CAS Number
96561-04-5
Purity
≥ 98% (HPLC)
Molecular Formula
C13H21F3N2O5
Molecular Weight
342.3
MDL Number
MFCD00236857
PubChem ID
295485
Melting Point
103-109 °C
Optical Rotation
[a]D22 = +3 ± 2º (C=1 in Acetone)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities for drug development.
  • Bioconjugation: It is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of therapeutic agents in targeted drug delivery systems.
  • Protein Modification: The chemical is valuable for modifying proteins, enabling scientists to study protein interactions and functions, which is crucial in understanding various biological processes.
  • Research in Drug Design: Its unique trifluoroacetyl group provides advantages in drug design, offering researchers insights into structure-activity relationships that can lead to the development of more effective pharmaceuticals.
  • Development of Diagnostic Tools: This compound is also employed in the creation of diagnostic tools, aiding in the detection of diseases through improved specificity and sensitivity in assays.

Citations