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Catalog Number:
03098
CAS Number:
13288-57-8
Nε-Boc-L-lysine tert-butyl ester hydrochloride
Purity:
≥ 98%
Synonym(s):
L-Lys(Boc)-OtBu·HCl
Documents
$51.18 /1G
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Product Information

Ne-Boc-L-lysine tert-butyl ester hydrochloride is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyl protective group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure allows for selective deprotection, facilitating the synthesis of bioactive peptides and other compounds with specific biological activities.

In the pharmaceutical industry, Ne-Boc-L-lysine tert-butyl ester hydrochloride serves as a key intermediate in the development of therapeutics, particularly in the design of peptide-based drugs. Its application extends to the production of drug delivery systems and the creation of novel biomaterials. Researchers appreciate its ease of handling and compatibility with various coupling reagents, which streamlines the synthesis process. This compound not only enhances the efficiency of peptide synthesis but also contributes to the development of innovative solutions in drug formulation and delivery.

Synonyms
L-Lys(Boc)-OtBu·HCl
CAS Number
13288-57-8
Purity
≥ 98%
Molecular Formula
C15H30N2O4·HCl
Molecular Weight
338.9
MDL Number
MFCD00038899
PubChem ID
24194132
Appearance
White powder
Optical Rotation
[a]D20 = +13.0 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Lys(Boc)-OtBu·HCl
CAS Number
13288-57-8
Purity
≥ 98%
Molecular Formula
C15H30N2O4·HCl
Molecular Weight
338.9
MDL Number
MFCD00038899
PubChem ID
24194132
Appearance
White powder
Optical Rotation
[a]D20 = +13.0 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ne-Boc-L-lysine tert-butyl ester hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protected amino acid in the synthesis of peptides, allowing for the selective introduction of lysine residues while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in creating prodrugs that enhance bioavailability and reduce side effects.
  • Bioconjugation: The tert-butyl ester group facilitates the conjugation of biomolecules, aiding in the development of targeted drug delivery systems and diagnostic agents.
  • Protein Engineering: Researchers use it to modify proteins, enhancing their stability and functionality, which is essential in therapeutic applications.
  • Research in Molecular Biology: It is employed in various molecular biology techniques, including the study of protein interactions and functions, providing insights into cellular processes.

Citations