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Catalog Number:
01330
CAS Number:
102185-38-6
Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-Arg(Mtr)-OH
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$36.65 /1G
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Product Information

Na-Boc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound is particularly valued for its ability to facilitate the introduction of sulfonamide functionalities into peptides, enhancing their stability and bioactivity. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for researchers focused on developing complex peptide-based therapeutics.

In the pharmaceutical industry, Na-Boc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is utilized in the design of novel drug candidates, particularly those targeting specific biological pathways. Its compatibility with various coupling reagents and its ability to enhance solubility in aqueous environments further underscore its utility in drug formulation. Researchers can leverage this compound to create more effective and targeted therapies, making it a valuable addition to any synthetic chemistry toolkit.

Synonyms
Boc-L-Arg(Mtr)-OH
CAS Number
102185-38-6
Purity
≥ 98% (HPLC)
Molecular Formula
C21H34N4O7S
Molecular Weight
486.68
MDL Number
MFCD00043097
Appearance
White to off-white powder
Optical Rotation
[a]D24 = +3 ± 0.5º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Arg(Mtr)-OH
CAS Number
102185-38-6
Purity
≥ 98% (HPLC)
Molecular Formula
C21H34N4O7S
Molecular Weight
486.68
MDL Number
MFCD00043097
Appearance
White to off-white powder
Optical Rotation
[a]D24 = +3 ± 0.5º (C=1 in MeOH)
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-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of peptide-based therapeutics, enhancing the specificity and efficacy of drug candidates.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Protein Modification: The compound is used to modify proteins, aiding in the study of protein interactions and functions, which is essential for understanding various biological processes.
  • Research in Drug Development: Its unique structure allows for the exploration of new drug candidates, particularly in the field of oncology and infectious diseases, where targeted therapies are increasingly important.
  • Analytical Chemistry: It can be utilized in analytical methods to detect and quantify specific biomolecules, providing insights into metabolic pathways and disease states.

Citations