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Catalog Number:
31312
CAS Number:
190656-01-0
N -Fmoc-hydroxylamine
Purity:
≥ 99 % (HPLC)
Synonym(s):
9-Fluorénylméthyl N -hydroxycarbamate
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Product Information

N-Fmoc-hydroxylamine is a versatile and valuable reagent widely utilized in organic synthesis and peptide chemistry. This compound serves as a protective group for amines, allowing for selective reactions without interference from other functional groups. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, enhances its stability and solubility, making it an ideal choice for researchers looking to streamline their synthetic pathways. N-Fmoc-hydroxylamine is particularly beneficial in the synthesis of peptide derivatives and in the development of pharmaceuticals, where precise control over functional groups is essential.

In addition to its applications in peptide synthesis, N-Fmoc-hydroxylamine has shown promise in the field of medicinal chemistry, where it can be employed in the design of bioactive compounds. Its ability to facilitate the introduction of hydroxylamine functionalities allows for the creation of novel molecules with potential therapeutic effects. Researchers and industry professionals appreciate its reliability and efficiency, making it a preferred choice for those aiming to enhance their synthetic methodologies.

Synonyms
9-Fluorénylméthyl N -hydroxycarbamate
CAS Number
190656-01-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 13 NON 3
Molecular Weight
255.27
MDL Number
MFCD01862911
PubChem ID
5062222
Melting Point
168-175 ?C
Appearance
Poudre blanche
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
9-Fluorénylméthyl N -hydroxycarbamate
CAS Number
190656-01-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 13 NON 3
Molecular Weight
255.27
MDL Number
MFCD01862911
PubChem ID
5062222
Melting Point
168-175 ?C
Appearance
Poudre blanche
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Fmoc-hydroxylamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for amines during peptide synthesis, allowing for selective reactions and improving yield and purity.
  • Drug Development: It plays a crucial role in the modification of drug candidates, particularly in enhancing their pharmacological properties and bioavailability.
  • Analytical Chemistry: Used in the derivatization of carbonyl compounds, it aids in the detection and quantification of various analytes in complex mixtures.
  • Bioconjugation: This chemical facilitates the attachment of biomolecules, such as proteins and nucleic acids, to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Material Science: It is employed in the development of functionalized polymers and materials, contributing to innovations in coatings and adhesives with enhanced performance characteristics.

Citations