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Catalog Number:
06131
CAS Number:
172422-76-3
Nε-Boc-L-lysine 4-nitroanilide
Purity:
≥ 99% (HPLC)
Synonym(s):
L-Lys(Boc)-pNA
Documents
$100.05 /1G
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Product Information

Ne-Boc-L-lysine 4-nitroanilide is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This protected amino acid derivative features a tert-butoxycarbonyl (Boc) group, which enhances its stability and solubility, making it an excellent choice for researchers in the fields of medicinal chemistry and biochemistry. The presence of the 4-nitroanilide moiety allows for selective reactions, facilitating the development of complex biomolecules and therapeutic agents.

This compound is particularly valuable in the synthesis of peptide-based drugs and can be employed in the preparation of various bioactive peptides. Its unique structure not only aids in the formation of peptide bonds but also provides functional groups that can be further modified for specific applications. Researchers appreciate its ability to streamline the synthesis process while maintaining high yields and purity, making Ne-Boc-L-lysine 4-nitroanilide a preferred choice for those looking to innovate in drug development and protein engineering.

Synonyms
L-Lys(Boc)-pNA
CAS Number
172422-76-3
Purity
≥ 99% (HPLC)
Molecular Formula
C17H26N4O5
Molecular Weight
366.38
MDL Number
MFCD00237144
PubChem ID
74765203
Melting Point
91-97 °C
Appearance
White to light yellow crystalline powder
Optical Rotation
[α]D20 = +30.0 ± 2º (C=0.76 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Lys(Boc)-pNA
CAS Number
172422-76-3
Purity
≥ 99% (HPLC)
Molecular Formula
C17H26N4O5
Molecular Weight
366.38
MDL Number
MFCD00237144
PubChem ID
74765203
Melting Point
91-97 °C
Appearance
White to light yellow crystalline powder
Optical Rotation
[α]D20 = +30.0 ± 2º (C=0.76 in MeOH)
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

Ne-Boc-L-lysine 4-nitroanilide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly for creating modified peptides with specific functional groups, enhancing the versatility of peptide-based drugs.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for imaging applications, helping scientists visualize biological processes in real-time.
  • Enzyme Inhibition Studies: It acts as a substrate or inhibitor in enzyme assays, aiding in the study of enzyme kinetics and the development of enzyme inhibitors for therapeutic purposes.
  • Drug Development: Its unique structure allows for modifications that can lead to the development of new pharmaceuticals, particularly in the fields of oncology and infectious diseases.

Citations