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Catalog Number:
47704
CAS Number:
2304536-78-3
Fmoc-TEPA(Boc3)-Suc-OH
Purity:
≥ 98% (HPLC, TLC)
Synonym(s):
3‐(2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl][2‐{[(9H‐luoren‐‐l)methoxy]carbonyl}amino)ethyl]amino}ethyl)amino}ethyl)amino}ethyl)carbamoyl]propanoic acid
Documents
$155.00 /25MG
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Product Information

Fmoc-TEPA(Boc3)-Suc-OH is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a unique combination of Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) protecting groups, which facilitate the selective functionalization of peptides. Its structure allows for efficient coupling reactions, making it an essential building block in the synthesis of complex peptides and peptidomimetics. Researchers in medicinal chemistry and biochemistry can leverage this compound for the development of targeted therapeutics, particularly in the fields of cancer research and vaccine development.

The compound's stability under various reaction conditions and its compatibility with automated synthesizers make it an ideal choice for high-throughput applications. Additionally, Fmoc-TEPA(Boc3)-Suc-OH offers advantages over similar compounds by providing enhanced solubility and reactivity, which can lead to improved yields in peptide synthesis. Its unique properties and practical applications make it a valuable asset for researchers aiming to innovate in peptide-based therapies.

Synonyms
3‐(2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl][2‐{[(9H‐luoren‐‐l)methoxy]carbonyl}amino)ethyl]amino}ethyl)amino}ethyl)amino}ethyl)carbamoyl]propanoic acid
CAS Number
2304536-78-3
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C42H61N5O11
Molecular Weight
812.0
Appearance
White powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3‐(2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl](2‐{[(tert‐utoxy)carbonyl][2‐{[(9H‐luoren‐‐l)methoxy]carbonyl}amino)ethyl]amino}ethyl)amino}ethyl)amino}ethyl)carbamoyl]propanoic acid
CAS Number
2304536-78-3
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C42H61N5O11
Molecular Weight
812.0
Appearance
White 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-TEPA(Boc3)-Suc-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules with specific biological activities.
  • Drug Development: Its role in drug formulation enables the development of targeted therapies, particularly in cancer and autoimmune diseases, enhancing treatment efficacy.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, facilitating the creation of biosensors and diagnostic tools.
  • Research in Neuroscience: It aids in the synthesis of neuropeptides, contributing to studies on brain function and potential treatments for neurological disorders.
  • Material Science: The compound is applied in the development of functional materials, such as hydrogels, which are useful in drug delivery systems and tissue engineering.

Citations