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Catalog Number:
33503
CAS Number:
868594-41-6
Fmoc-2-(2-[2-(2-aminoethoxy)ethoxy]ethoxy)ethanol
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-AEEEE
Documents
$90.00 /100MG
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Product Information

Fmoc-2-(2-[2-(2-aminoethoxy)ethoxy]ethoxy)ethanol is a versatile compound widely utilized in the field of organic synthesis and peptide chemistry. This compound, known for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, serves as an essential building block in the synthesis of peptides and other complex organic molecules. Its unique structure, featuring multiple ethoxy linkages, enhances solubility and stability, making it particularly valuable in various chemical reactions. Researchers and industry professionals appreciate its role in facilitating the synthesis of bioactive peptides, which are crucial in pharmaceuticals and biotechnology applications.

The compound's ability to provide a protective group that can be easily removed under mild conditions allows for greater flexibility in synthetic pathways. This characteristic is especially beneficial in the development of peptide-based drugs and therapeutic agents. Additionally, its compatibility with automated synthesizers streamlines the peptide synthesis process, improving efficiency and yield. With its robust properties and practical applications, Fmoc-2-(2-[2-(2-aminoethoxy)ethoxy]ethoxy)ethanol stands out as a key reagent for researchers aiming to innovate in peptide synthesis and related fields.

Synonyms
Fmoc-AEEEE
CAS Number
868594-41-6
Purity
≥ 98% (HPLC)
Molecular Formula
C23H29NO6
Molecular Weight
415.5
MDL Number
MFCD31657165
PubChem ID
57884372
Appearance
Light yellow oil
Conditions
Store at -15 to -25 °C
General Information
Synonyms
Fmoc-AEEEE
CAS Number
868594-41-6
Purity
≥ 98% (HPLC)
Molecular Formula
C23H29NO6
Molecular Weight
415.5
MDL Number
MFCD31657165
PubChem ID
57884372
Appearance
Light yellow oil
Conditions
Store at -15 to -25 °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-(2-aminoethoxy)ethoxy]ethoxy)ethanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in modifying drug structures to improve solubility and bioavailability.
  • Bioconjugation: The compound is used 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 applied in the synthesis of functionalized polymers, which can be tailored for specific applications in materials science and nanotechnology.
  • Research in Biochemistry: The compound aids in studying enzyme activity and protein interactions, providing insights into biological processes and potential therapeutic targets.

Citations