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Catalog Number:
39659
CAS Number:
1952360-91-6
Acide (Fmoc-amino)-PEG 12 -C2-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 1-(9 H -fluorén-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31,34,37,40-tridécaoxa-4-azatritétracontane-43-oïque, Carboxy-PEG12-(Fmoc-amine)
Documents
$165.15 /100 mg
Taille
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Informations sur le produit

(Fmoc-amino)-PEG12-C2-carboxylic acid is a versatile compound widely utilized in bioconjugation and drug delivery applications. This compound features a polyethylene glycol (PEG) backbone, which enhances solubility and biocompatibility, making it an ideal choice for researchers working in the fields of medicinal chemistry and biochemistry. The Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of peptide conjugates and other biomolecules. Its unique structure promotes efficient conjugation to various biomolecules, enabling the development of targeted therapies and diagnostic agents.

In practical applications, (Fmoc-amino)-PEG12-C2-carboxylic acid is particularly valuable in the design of drug delivery systems, where it can improve the pharmacokinetics of therapeutic agents. Additionally, it is used in the creation of functionalized surfaces for biosensors and in the development of advanced materials for tissue engineering. The compound's ability to enhance stability and reduce immunogenicity makes it a preferred choice for researchers aiming to optimize the efficacy of their formulations.

Numéro CAS 
1952360-91-6
Formule moléculaire
C 42 H 6516
Poids moléculaire 
839.97
Informations générales
Numéro CAS 
1952360-91-6
Formule moléculaire
C 42 H 6516
Poids moléculaire 
839.97
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-amino)-PEG12-C2-carboxylic acid is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies.
  • Drug Delivery Systems: Its amphiphilic nature makes it ideal for formulating drug delivery systems, improving the solubility and bioavailability of hydrophobic drugs, which is particularly beneficial in pharmaceutical applications.
  • Polymer Chemistry: In polymer synthesis, it acts as a building block for creating functionalized polymers, which can be tailored for specific applications in materials science, such as coatings or adhesives.
  • Diagnostics: The compound is used in the development of diagnostic tools, where its ability to form stable conjugates with biomolecules aids in the creation of sensitive assays for disease detection.
  • Research in Nanotechnology: It plays a significant role in the fabrication of nanomaterials, enhancing their stability and functionality, which is crucial for advancements in nanomedicine and environmental applications.

Citations