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Catalog Number:
03954
CAS Number:
76052-29-4
Nα-Boc-Nω,Nω'-bis-Z-L-arginine N-hydroxysuccinimide ester
Synonym(s):
Boc-L-Arg(Z)2-OSu
Documents
$125.00 /250MG
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Product Information

Na-Boc-Nw,Nw'-bis-Z-L-arginine N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique structure that enhances its reactivity, making it an excellent choice for researchers looking to develop complex peptides and proteins. Its N-hydroxysuccinimide ester functionality allows for efficient coupling reactions with amines, facilitating the formation of stable amide bonds. This property is particularly advantageous in the pharmaceutical industry for drug development and in the production of targeted therapeutics.

Moreover, Na-Boc-Nw,Nw'-bis-Z-L-arginine N-hydroxysuccinimide ester is recognized for its ability to improve solubility and stability of peptides, which is crucial for maintaining bioactivity in various applications. Researchers in the fields of biochemistry and molecular biology can leverage this compound for the synthesis of modified peptides that exhibit enhanced pharmacological properties. Its compatibility with various coupling strategies makes it a preferred choice for professionals aiming to streamline their synthesis processes while achieving high yields and purity.

Synonyms
Boc-L-Arg(Z)2-OSu
CAS Number
76052-29-4
Molecular Formula
C31H37N5O10
Molecular Weight
639.6
MDL Number
MFCD00236826
PubChem ID
91976464
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Arg(Z)2-OSu
CAS Number
76052-29-4
Molecular Formula
C31H37N5O10
Molecular Weight
639.6
MDL Number
MFCD00236826
PubChem ID
91976464
Appearance
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-Boc-Nw,Nw'-bis-Z-L-arginine N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating complex structures that require specific amino acid sequences. Its protective groups facilitate selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is employed to modify bioactive peptides, improving their stability and bioavailability. This application is crucial in developing therapeutic agents that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This is particularly beneficial in creating targeted drug delivery systems and diagnostic tools.
  • Protein Engineering: Researchers utilize it in protein engineering to introduce specific modifications to proteins, enhancing their functionality or stability. This is essential in developing proteins for therapeutic applications.
  • Research in Immunology: It plays a role in immunological studies by aiding in the design of peptide-based vaccines. Its ability to enhance immune responses makes it a key component in vaccine development.

Citations