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Catalog Number:
16937
CAS Number:
817169-73-6
N α -Fmoc- N δ -(N-biotinyl-3-(2-(2-(3-aminopropyloxy)-éthoxy)-éthoxypropyl)-L-glutamine
Purity:
≥ 97 % (CCM)
Synonym(s):
Fmoc-L-Gln(biotinyl-PEG)-OH
Documents
95 /100
2 Citations
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$95.60 /100 mg
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Informations sur le produit

Na-Fmoc-Nd-(N-biotinyl-3-(2-(2-(3-aminopropyloxy)-ethoxy)-ethoxypropyl)-L-glutamine is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This compound features a unique structure that combines the properties of biotin and Fmoc (9-fluorenylmethoxycarbonyl), making it an excellent choice for peptide synthesis and bioconjugation. Its ability to facilitate the attachment of biomolecules to surfaces or other compounds enhances its utility in various applications, including drug delivery systems, targeted therapies, and diagnostic assays. Researchers appreciate its stability and ease of use, which streamline experimental workflows and improve reproducibility.

Moreover, Na-Fmoc-Nd-(N-biotinyl-3-(2-(2-(3-aminopropyloxy)-ethoxy)-ethoxypropyl)-L-glutamine offers significant advantages over similar compounds, particularly in its biocompatibility and functionalization capabilities. This makes it an ideal candidate for developing innovative solutions in molecular biology, such as creating biotinylated probes for imaging or affinity purification techniques. Its multifunctional nature and compatibility with various experimental setups position it as a valuable tool for researchers aiming to explore new frontiers in life sciences.

Numéro CAS 
817169-73-6
Formule moléculaire
C 40 H 55 N 5 O 10 S
Poids moléculaire 
798.0
Rotation optique 
[a] D 25 = 23 ± 2,5 º (C = 1 dans MeOH)
Informations générales
Numéro CAS 
817169-73-6
Formule moléculaire
C 40 H 55 N 5 O 10 S
Poids moléculaire 
798.0
Rotation optique 
[a] D 25 = 23 ± 2,5 º (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Na-Fmoc-Nd-(N-biotinyl-3-(2-(2-(3-aminopropyloxy)-ethoxy)-ethoxypropyl)-L-glutamine is widely utilized in research focused on:

  • Bioconjugation: This compound is essential for attaching biomolecules like proteins or antibodies to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Peptide Synthesis: It plays a crucial role in solid-phase peptide synthesis, allowing researchers to create complex peptides for therapeutic and diagnostic applications.
  • Cell Biology: Used in cell labeling and tracking, it aids in studying cellular processes and interactions, providing insights into disease mechanisms.
  • Diagnostics: The biotinylation feature enables the development of sensitive assays for detecting biomolecules, improving the accuracy of diagnostic tests.
  • Drug Development: Its ability to facilitate the design of peptide-based drugs enhances the efficiency of pharmaceutical research, leading to innovative therapies.

Citations