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Catalog Number:
33502
CAS Number:
560088-66-6
Fmoc-2-(2-(2-aminoethoxy)ethoxy)ethanol
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-AEEE
Documents
$72.31 /100MG
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Product Information

Fmoc-2-(2-(2-aminoethoxy)ethoxy)ethanol is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, serves as a crucial building block in the synthesis of peptides, allowing for selective deprotection and facilitating the formation of complex molecular structures. Its unique structure, featuring multiple ethoxy groups, enhances solubility and stability, making it an ideal choice for researchers working in organic chemistry and biochemistry.

In practical applications, Fmoc-2-(2-(2-aminoethoxy)ethoxy)ethanol is particularly beneficial in the development of pharmaceuticals, where precise control over peptide sequences is essential. It is also used in the preparation of various biomolecules, contributing to advancements in drug delivery systems and therapeutic agents. Researchers appreciate its ease of use and compatibility with standard peptide synthesis protocols, which streamline the development process and improve overall efficiency.

Synonyms
Fmoc-AEEE
CAS Number
560088-66-6
Purity
≥ 99% (HPLC)
Molecular Formula
C21H25NO5
Molecular Weight
371.4
MDL Number
MFCD08669697
PubChem ID
17039577
Melting Point
41 - 47 ?C
Appearance
White crystalline powder
Conditions
Store at 2-8 °C
General Information
Synonyms
Fmoc-AEEE
CAS Number
560088-66-6
Purity
≥ 99% (HPLC)
Molecular Formula
C21H25NO5
Molecular Weight
371.4
MDL Number
MFCD08669697
PubChem ID
17039577
Melting Point
41 - 47 ?C
Appearance
White crystalline powder
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-2-(2-(2-aminoethoxy)ethoxy)ethanol 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 Development: It is used in the development of pharmaceutical compounds, particularly in creating prodrugs that enhance bioavailability and solubility, improving therapeutic efficacy.
  • Bioconjugation: The chemical plays a crucial role in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Polymer Chemistry: It is employed in the synthesis of functionalized polymers, contributing to the development of materials with specific properties for applications in coatings and adhesives.
  • Diagnostic Tools: The compound is utilized in the production of diagnostic agents, enhancing the sensitivity and specificity of assays used in medical testing and research.

Citations