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Catalog Number:
00146
CAS Number:
98930-01-9
N α -Fmoc- N ω -(4-metoxi-2,3,6-trimetilbencenosulfonil)-L-arginina
Purity:
≥ 99 % (HPLC, TLC)
Synonym(s):
Fmoc-L-Arg(Mtr)-OH
Documents
$22.83 /1G
Tamaño
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Product Information

La protección Mtr-guanidina de arg es más sensible al ácido que el grupo tosilo.

Synonyms
Fmoc-L-Arg(Mtr)-OH
CAS Number
98930-01-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C31H36N4O7S
Molecular Weight
608.9
MDL Number
MFCD00043098
PubChem ID
3383824
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] 20 D = -5,0 ± 1,0 °
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Arg(Mtr)-OH
CAS Number
98930-01-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C31H36N4O7S
Molecular Weight
608.9
MDL Number
MFCD00043098
PubChem ID
3383824
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] 20 D = -5,0 ± 1,0 °
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The compound can be used to attach peptides to various biomolecules, facilitating the development of targeted drug delivery systems and diagnostic agents.
  • Research in Biochemistry: It is valuable in studying protein interactions and functions, providing insights into cellular processes and disease mechanisms.
  • Custom Synthesis: Researchers can utilize this compound for tailored peptide sequences, enabling the exploration of specific biological pathways and therapeutic targets.

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