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Catalog Number:
05686
CAS Number:
214852-34-3
Nα-Fmoc-Nω,Nω'-bis-Boc-D-arginine
Purity:
≥ 98%
Synonym(s):
Fmoc-D-Arg(Boc)2-OH
Documents
$221.63 /250MG
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Product Information

Na-Fmoc-Nw,Nw'-bis-Boc-D-arginine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique combination of protective groups that enhance its stability and reactivity, making it an ideal choice for researchers in the fields of biochemistry and medicinal chemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) protecting groups facilitate the selective deprotection of amino acids during solid-phase peptide synthesis, allowing for the efficient assembly of complex peptides with high purity and yield.

This compound is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of bioactive peptides, which can be used in drug discovery and development, as well as in the creation of novel biomaterials. Researchers appreciate Na-Fmoc-Nw,Nw'-bis-Boc-D-arginine for its ability to enhance solubility and stability in various solvents, making it a preferred choice for complex peptide formulations.

Synonyms
Fmoc-D-Arg(Boc)2-OH
CAS Number
214852-34-3
Purity
≥ 98%
Molecular Formula
C31H40N4O8
Molecular Weight
596.7
MDL Number
MFCD00798643
PubChem ID
59693726
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Arg(Boc)2-OH
CAS Number
214852-34-3
Purity
≥ 98%
Molecular Formula
C31H40N4O8
Molecular Weight
596.7
MDL Number
MFCD00798643
PubChem ID
59693726
Appearance
White to off-white powder
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-Fmoc-Nw,Nw'-bis-Boc-D-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of peptide-based drugs. Its protective groups facilitate the selective modification of amino acids, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel therapeutic peptides that can target specific biological pathways, offering potential treatments for various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The compound's functional groups allow for easy conjugation with other biomolecules, making it valuable in the creation of targeted drug delivery systems and diagnostic agents in the field of biomedicine.
  • Research on Protein Interactions: It aids in studying protein-protein interactions by providing a means to modify proteins, which can help researchers understand complex biological processes and develop new therapeutic strategies.
  • Customizable Research Tools: The versatility of this compound allows researchers to tailor it for specific applications, making it an essential tool in both academic and industrial laboratories for advancing biochemical research.

Citations