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Catalog Number:
46597
CAS Number:
756526-02-0
Fmoc-NH-(PEG) 8 - CH2CH2COOH
Purity:
≥ 97%
Synonym(s):
Acide 1-(Fmoc-amino)-3,6,9,12,15,18,21,24-octaoxaheptacosan-27-oïque
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$70.50 /100 mg
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Informations sur le produit

Fmoc-NH-(PEG)8-CH2CH2COOH is a versatile compound that combines the benefits of polyethylene glycol (PEG) with the protective Fmoc (fluorenylmethyloxycarbonyl) group, making it an essential tool in peptide synthesis and drug delivery applications. This compound features a long PEG chain, which enhances solubility and biocompatibility, making it particularly useful in pharmaceutical formulations and biomedical research. Its unique structure allows for the efficient conjugation of peptides and proteins, facilitating targeted drug delivery systems that can improve therapeutic efficacy while minimizing side effects.

Researchers and industry professionals can leverage Fmoc-NH-(PEG)8-CH2CH2COOH in various applications, including the development of advanced drug delivery vehicles, bioconjugates, and surface modifications for biomaterials. Its ability to provide a hydrophilic environment while maintaining stability under physiological conditions makes it ideal for enhancing the performance of therapeutic agents. By incorporating this compound into their projects, professionals can expect improved solubility, stability, and overall effectiveness of their formulations.

Numéro CAS 
756526-02-0
Formule moléculaire
C 34 H 4912
Poids moléculaire 
663.75
Informations générales
Numéro CAS 
756526-02-0
Formule moléculaire
C 34 H 4912
Poids moléculaire 
663.75
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-NH-(PEG)8-CH2CH2COOH is widely utilized in research focused on:

  • Bioconjugation: This compound serves as an effective linker in bioconjugation processes, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing their functionality in drug delivery systems.
  • Drug Delivery: Its PEG (polyethylene glycol) component improves solubility and biocompatibility, making it ideal for formulating drug delivery systems that can target specific tissues or cells, thus increasing therapeutic efficacy.
  • Peptide Synthesis: The Fmoc protecting group is widely used in solid-phase peptide synthesis, enabling the creation of complex peptides with high purity, which are essential for various biological applications.
  • Biomedical Research: This compound is valuable in developing hydrogels for tissue engineering, providing a scaffold that supports cell growth and differentiation, which is crucial for regenerative medicine.
  • Diagnostics: It can be employed in the development of diagnostic tools, such as biosensors, where its ability to modify surfaces enhances the sensitivity and specificity of detection methods.

Citations