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Catalog Number:
22666
CAS Number:
613245-91-3
N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-(PEG)2-Suc-OH
Documents
$58.39 /250MG
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Product Information

N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure incorporates a long hydrophilic octyl chain, enhancing solubility in various organic solvents, making it particularly useful in organic synthesis and bioconjugation applications. Researchers appreciate its ability to facilitate the formation of stable peptide bonds, which is crucial in the development of therapeutic peptides and proteins.

In addition to its role in peptide synthesis, N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is also explored for its potential in drug delivery systems due to its biocompatibility and ability to form micelles. These properties make it an attractive candidate for targeted drug delivery applications, particularly in cancer therapy where precise delivery of therapeutic agents is paramount. Its unique combination of hydrophilicity and functionality positions it as a valuable tool for researchers and industry professionals focused on advancing peptide-based therapeutics and innovative drug delivery solutions.

Synonyms
Fmoc-(PEG)2-Suc-OH
CAS Number
613245-91-3
Purity
≥ 98% (HPLC)
Molecular Formula
C25H30N2O7
Molecular Weight
470.52
MDL Number
MFCD06656466
PubChem ID
2756180
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-(PEG)2-Suc-OH
CAS Number
613245-91-3
Purity
≥ 98% (HPLC)
Molecular Formula
C25H30N2O7
Molecular Weight
470.52
MDL Number
MFCD06656466
PubChem ID
2756180
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

N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial for creating complex peptides with specific functionalities.
  • Drug Development: Its unique structure enhances solubility and bioavailability of pharmaceutical compounds, making it valuable in the formulation of new drugs, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps to link biomolecules such as proteins and antibodies to therapeutic agents, improving the efficacy of treatments in fields like oncology.
  • Material Science: In the development of smart materials, this chemical can be incorporated into polymers to create responsive materials that change properties under specific conditions, useful in sensors and drug delivery systems.
  • Research in Nanotechnology: It plays a role in the synthesis of nanoparticles for drug delivery applications, providing a stable and functional surface for attaching therapeutic agents, enhancing targeted delivery and reducing side effects.

Citations