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Catalog Number:
05452
CAS Number:
97745-69-2
Nα,Nω,Nω'-Tris-Boc-L-arginine
Purity:
99 - 101% (Assay by titration)
Synonym(s):
Boc-L-Arg(Boc)2-OH
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Product Information

Na,Nw,Nw'-Tris-Boc-L-arginine is a highly versatile compound widely utilized in the fields of biochemistry and pharmaceutical research. This protected form of L-arginine features three Boc (tert-butyloxycarbonyl) groups, which enhance its stability and solubility, making it an ideal choice for peptide synthesis and drug development. Researchers often employ this compound in the design of novel peptides and proteins, particularly in studies related to nitric oxide production and cardiovascular health. Its unique structure allows for selective modification, facilitating the exploration of various biological activities and therapeutic applications.

In addition to its role in peptide synthesis, Na,Nw,Nw'-Tris-Boc-L-arginine is also valuable in the development of drug delivery systems and as a building block for bioactive compounds. Its ability to enhance cellular uptake and bioavailability makes it a preferred choice for formulating therapeutic agents. With its robust properties and practical applications, this compound stands out as an essential tool for researchers aiming to innovate in the fields of drug design and molecular biology.

Synonyms
Boc-L-Arg(Boc)2-OH
CAS Number
97745-69-2
Purity
99 - 101% (Assay by titration)
Molecular Formula
C21H38N4O8
Molecular Weight
474.56
MDL Number
MFCD00236819
PubChem ID
15311268
Melting Point
116 - 120 ?C (Lit.)
Appearance
White powder
Optical Rotation
[a]D24 = -5 ± 2 º (C=1 in DMF)
Conditions
Store at ≤ -15 °C
General Information
Synonyms
Boc-L-Arg(Boc)2-OH
CAS Number
97745-69-2
Purity
99 - 101% (Assay by titration)
Molecular Formula
C21H38N4O8
Molecular Weight
474.56
MDL Number
MFCD00236819
PubChem ID
15311268
Melting Point
116 - 120 ?C (Lit.)
Appearance
White powder
Optical Rotation
[a]D24 = -5 ± 2 º (C=1 in DMF)
Conditions
Store at ≤ -15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na,Nw,Nw'-Tris-Boc-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. Its use simplifies the process and enhances yield.
  • Drug Development: In pharmaceutical research, it is employed in the design of arginine-based drugs, which can improve drug solubility and bioavailability, making medications more effective.
  • Bioconjugation: The compound is useful in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Gene Delivery Systems: It plays a role in developing non-viral gene delivery systems, improving the efficiency of delivering genetic material into cells, which is crucial for gene therapy applications.
  • Research on Cardiovascular Health: Researchers study its effects on nitric oxide production, which is vital for cardiovascular health, potentially leading to new treatments for heart-related conditions.

Citations