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Catalog Number:
26455
CAS Number:
872679-70-4
Fmoc-AEEP-OH
Purity:
≥ 99% (Assay by titration)
Documents
$40.00 /100MG
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Product Information

Fmoc-AEEP-OH is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process and facilitates the selective deprotection of the amino group. Its unique structure, characterized by the ethoxy linkers, enhances solubility and reactivity, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds.

In practical applications, Fmoc-AEEP-OH is particularly valuable in the synthesis of peptide-based therapeutics, where precision and efficiency are paramount. Its ability to streamline the synthesis process allows for the rapid development of novel peptides, which can be crucial in fields such as drug discovery and biomolecular research. Additionally, the Fmoc protection strategy is well-established, ensuring compatibility with various coupling reagents and methodologies. Researchers can leverage Fmoc-AEEP-OH to create tailored peptides with specific functionalities, paving the way for advancements in medicinal chemistry and biotechnology.

CAS Number
872679-70-4
Purity
≥ 99% (Assay by titration)
Molecular Formula
C22H25NO6
Molecular Weight
399.44
MDL Number
MFCD08064306
PubChem ID
51340973
Melting Point
94 - 102 ?C
Appearance
White crystalline powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
872679-70-4
Purity
≥ 99% (Assay by titration)
Molecular Formula
C22H25NO6
Molecular Weight
399.44
MDL Number
MFCD08064306
PubChem ID
51340973
Melting Point
94 - 102 ?C
Appearance
White crystalline powder
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-AEEP-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with the overall peptide structure.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: Fmoc-AEEP-OH is used in bioconjugation techniques to attach peptides to various biomolecules, facilitating the creation of targeted drug delivery systems.
  • Research in Molecular Biology: Researchers utilize this compound in the study of protein interactions and functions, aiding in the understanding of complex biological processes.
  • Custom Synthesis: Its versatility allows for the custom synthesis of modified peptides, catering to specific research needs in academic and pharmaceutical laboratories.

Citations