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Catalog Number:
26462
CAS Number:
93372-25-9
Ácido fmoc-2,2,6,6-tetrametilpiperidina- N -oxil-4-amino-4-carboxílico
Purity:
≥ 99 % (HPLC, TLC)
Synonym(s):
Fmoc-Toac-OH
Documents
$166.00 /100 mg
Tamaño
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Product Information

Fmoc-2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and peptide chemistry. This stable nitroxide radical is particularly valued for its role as a spin label in electron paramagnetic resonance (EPR) spectroscopy, allowing researchers to study molecular dynamics and interactions in biological systems. Its unique structure enhances the stability and solubility of peptides, making it an excellent choice for applications in drug design and development.

In addition to its use in EPR studies, this compound serves as a powerful tool for the synthesis of various bioactive molecules, enabling the development of novel therapeutics. Its ability to facilitate the introduction of functional groups into peptides and proteins opens up new avenues for research in medicinal chemistry and biochemistry. With its robust properties and practical applications, Fmoc-2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid stands out as an essential reagent for professionals seeking to advance their research and product development efforts.

Synonyms
Fmoc-Toac-OH
CAS Number
93372-25-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C25H30N2O5
Molecular Weight
438.52
MDL Number
MFCD03425569
Melting Point
150 - 170 ?C
Appearance
Polvo cristalino de color amarillo claro
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
Fmoc-Toac-OH
CAS Number
93372-25-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C25H30N2O5
Molecular Weight
438.52
MDL Number
MFCD03425569
Melting Point
150 - 170 ?C
Appearance
Polvo cristalino de color amarillo claro
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting others, which is crucial in developing complex peptides.
  • Radical Scavenging: Its unique structure enables it to act as a radical scavenger, making it valuable in studies related to oxidative stress and the development of antioxidants in pharmaceuticals.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in drug delivery systems and diagnostics.
  • Material Science: It finds applications in the development of advanced materials, particularly in creating polymers with specific properties, enhancing their performance in various industrial applications.
  • Medicinal Chemistry: Researchers utilize it in the design of new drugs, particularly those targeting specific biological pathways, due to its ability to modify molecular interactions effectively.

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