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Catalog Number:
31636
CAS Number:
1178899-92-7
N-N3-N-Boc-D-lysine
Purity:
≥99%
Synonym(s):
N3-D-Lys(Boc)-OH, (R-2-Azido-6-(Boc-amino)caproic acid
Documents
$43.87 /100MG
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Product Information

N3-D-Lys(Boc)-OH is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a protected lysine residue, making it an ideal building block for the development of peptide-based therapeutics and research applications. Its azido group allows for click chemistry reactions, enabling researchers to efficiently label biomolecules or create complex molecular structures. The Boc (tert-butyloxycarbonyl) protecting group provides stability during synthesis, ensuring high yields and purity in final products.

This compound is particularly valuable in the fields of medicinal chemistry and drug development, where it can be utilized to create targeted drug delivery systems or study protein interactions. Its unique properties facilitate the incorporation of functional groups, enhancing the versatility of peptide constructs. Researchers can leverage N3-D-Lys(Boc)-OH to explore innovative therapeutic strategies, making it an essential tool in modern biochemical research.

Synonyms
N3-D-Lys(Boc)-OH, (R-2-Azido-6-(Boc-amino)caproic acid
CAS Number
1178899-92-7
Purity
≥99%
Molecular Formula
C11H20N4O4
Molecular Weight
272.3
MDL Number
MFCD22989455
PubChem ID
57915538
Melting Point
60-66 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = +43 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
N3-D-Lys(Boc)-OH, (R-2-Azido-6-(Boc-amino)caproic acid
CAS Number
1178899-92-7
Purity
≥99%
Molecular Formula
C11H20N4O4
Molecular Weight
272.3
MDL Number
MFCD22989455
PubChem ID
57915538
Melting Point
60-66 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = +43 ± 2º (C=1 in DMF)
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

N3-D-Lys(Boc)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require the incorporation of azido groups for further functionalization.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, especially in creating compounds that can interact with biological targets through click chemistry.
  • Bioconjugation: The azido group allows for selective labeling and modification of biomolecules, making it valuable in the production of bioconjugates for diagnostic and therapeutic applications.
  • Research in Molecular Biology: It is used in various molecular biology applications, including the study of protein interactions and the development of novel assays.
  • Material Science: The compound is also explored in the creation of functionalized materials, which can be used in drug delivery systems and nanotechnology.

Citations