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Catalog Number:
03882
CAS Number:
2212-69-3
Nα-Z-Nε-Boc-L-lysine 4-nitrophenyl ester
Purity:
≥ 98% (TLC)
Synonym(s):
Z-L-Lys(Boc)-ONp
Documents
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Product Information

Na-Z-Ne-Boc-L-lysine 4-nitrophenyl ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This derivative of L-lysine features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and reactivity, making it an ideal choice for researchers focused on developing complex peptides and proteins. The presence of the 4-nitrophenyl ester group allows for selective cleavage under mild conditions, facilitating the release of the active amine when needed.

This compound is particularly valuable in the pharmaceutical and biotechnology industries, where it can be employed in the design of targeted drug delivery systems and the development of novel therapeutics. Its unique structure enables efficient coupling reactions, making it a preferred choice for synthesizing peptide-based drugs and biomolecules. Researchers can leverage Na-Z-Ne-Boc-L-lysine 4-nitrophenyl ester to streamline their workflows, enhance yields, and improve the overall efficiency of their synthetic processes.

Synonyms
Z-L-Lys(Boc)-ONp
CAS Number
2212-69-3
Purity
≥ 98% (TLC)
Molecular Formula
C25H31N3O8
Molecular Weight
501.54
MDL Number
MFCD00076963
PubChem ID
294898
Appearance
White powder
Optical Rotation
[a]D24 = -17.5 ± 1º (C=1 in Acetone)
Conditions
Store at 0-8 °C
General Information
Synonyms
Z-L-Lys(Boc)-ONp
CAS Number
2212-69-3
Purity
≥ 98% (TLC)
Molecular Formula
C25H31N3O8
Molecular Weight
501.54
MDL Number
MFCD00076963
PubChem ID
294898
Appearance
White powder
Optical Rotation
[a]D24 = -17.5 ± 1º (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-Z-Ne-Boc-L-lysine 4-nitrophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its unique properties make it valuable in medicinal chemistry for developing new pharmaceuticals, particularly those targeting specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules to enhance drug delivery systems or create targeted therapies, improving efficacy and reducing side effects.
  • Research in Protein Engineering: It aids in the modification of lysine residues in proteins, facilitating studies on protein function and interactions, which is crucial for understanding biological mechanisms.
  • Diagnostics: The compound can be employed in the development of diagnostic tools, particularly in assays that require specific interactions with biological molecules, enhancing sensitivity and specificity.

Citations