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Catalog Number:
22669
CAS Number:
882847-34-9
Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
Fmoc-NH-(PEG)5-COOH
Documents
$80.00 /100MG
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Product Information

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, is particularly valuable for researchers engaged in solid-phase peptide synthesis (SPPS). Its unique structure, which includes multiple ethylene glycol units, enhances solubility and stability, making it an ideal choice for synthesizing complex peptides and proteins.

The compound's ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the efficient assembly of biologically active molecules. Additionally, its application extends to the development of bioconjugates and drug delivery systems, where its hydrophilic nature aids in improving the pharmacokinetic properties of therapeutic agents. Researchers and industry professionals can leverage Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid to streamline their synthesis processes and enhance the efficacy of their products.

Synonyms
Fmoc-NH-(PEG)5-COOH
CAS Number
882847-34-9
Purity
≥ 95% (HPLC)
Molecular Formula
C30H41NO10
Molecular Weight
575.66
MDL Number
MFCD06656474
PubChem ID
2756188
Appearance
Colorless liquid or yellowish oil
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-NH-(PEG)5-COOH
CAS Number
882847-34-9
Purity
≥ 95% (HPLC)
Molecular Formula
C30H41NO10
Molecular Weight
575.66
MDL Number
MFCD06656474
PubChem ID
2756188
Appearance
Colorless liquid or yellowish oil
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-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Delivery Systems: Its unique structure enhances the solubility and stability of therapeutic agents, making it ideal for developing advanced drug delivery formulations.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies.
  • Polymer Chemistry: It is used in the synthesis of functionalized polymers, contributing to the development of materials with specific properties for applications in coatings and adhesives.
  • Research in Nanotechnology: The compound plays a role in the fabrication of nanostructures, enhancing the performance of nanoscale devices in electronics and medicine.

Citations