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Catalog Number:
12641
CAS Number:
1820604-77-0
Fmoc-N-ethyl-hydroxylamine
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$60.39 /250MG
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Product Information

Fmoc-N-ethyl-hydroxylamine is a versatile reagent widely utilized in organic synthesis and peptide chemistry. This compound serves as a protective group for amines, allowing for selective reactions without interfering with other functional groups. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, provides stability and ease of removal under mild conditions, making it an ideal choice for researchers focused on synthesizing complex molecules.

In addition to its protective capabilities, Fmoc-N-ethyl-hydroxylamine is particularly valuable in the development of pharmaceuticals and biologically active compounds. It has been effectively employed in the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial. The compound's ability to facilitate the introduction of hydroxylamine functionalities further enhances its utility in medicinal chemistry, enabling the creation of novel compounds with improved efficacy and selectivity. Researchers and industry professionals will find Fmoc-N-ethyl-hydroxylamine to be a reliable and efficient tool in their synthetic arsenal, streamlining processes and enhancing product yields.

CAS Number
1820604-77-0
Molecular Formula
C17H17NO3
Molecular Weight
283.3
MDL Number
MFCD02682861
PubChem ID
57574589
Conditions
Store at 0-8°C
General Information
CAS Number
1820604-77-0
Molecular Formula
C17H17NO3
Molecular Weight
283.3
MDL Number
MFCD02682861
PubChem ID
57574589
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

Fmoc-N-ethyl-hydroxylamine 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 other functional groups.
  • Drug Development: In medicinal chemistry, it aids in the design of new pharmaceuticals by facilitating the introduction of hydroxylamine functionalities, which can enhance biological activity.
  • Analytical Chemistry: It is employed in the derivatization of carbonyl compounds, improving detection and quantification in various analytical techniques such as HPLC and mass spectrometry.
  • Bioconjugation: This chemical plays a crucial role in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Material Science: It is used in the development of advanced materials, particularly in creating polymers with specific functional properties, which can be tailored for applications in coatings and adhesives.

Citations