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Catalog Number:
16470
CAS Number:
1864003-01-9
Z-D-Lys(Fmoc)-OH
Purity:
≥ 95% (HPLC)
Documents
$168.35 /1G
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Product Information

Z-D-Lys(Fmoc)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers aiming to create high-purity peptides for therapeutic applications.

In addition to its role in peptide synthesis, Z-D-Lys(Fmoc)-OH is also employed in the development of bioconjugates and in studies involving protein interactions. Its stability and compatibility with various coupling reagents enhance its utility in diverse chemical environments. Researchers in pharmaceutical and biotechnology sectors will find this compound particularly beneficial for developing novel therapeutics and studying protein structure-function relationships. With its reliable performance and ease of use, Z-D-Lys(Fmoc)-OH stands out as a key reagent for advancing peptide chemistry and related fields.

CAS Number
1864003-01-9
Purity
≥ 95% (HPLC)
Molecular Formula
C29H30N2O6
Molecular Weight
502.57
MDL Number
MFCD08458677
PubChem ID
13585940
Appearance
White or off-white solid
Optical Rotation
[a]D20 = +7 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
CAS Number
1864003-01-9
Purity
≥ 95% (HPLC)
Molecular Formula
C29H30N2O6
Molecular Weight
502.57
MDL Number
MFCD08458677
PubChem ID
13585940
Appearance
White or off-white solid
Optical Rotation
[a]D20 = +7 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Z-D-Lys(Fmoc)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide structures efficiently.
  • Drug Development: It is used in the development of peptide-based drugs, providing a framework for modifying biological activity and improving therapeutic efficacy in pharmaceuticals.
  • Bioconjugation: The compound aids in bioconjugation processes, where it can be linked to other biomolecules, enhancing the delivery and targeting of drugs in cancer therapy.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurological disorders.
  • Protein Engineering: This chemical is instrumental in modifying proteins to study their functions, stability, and interactions, which is crucial for advancements in biotechnology and synthetic biology.

Citations