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Catalog Number:
33488
CAS Number:
1662688-16-5
Fmoc-L-Lys(Boc-AEEA)-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Nα -Fmoc- Nε- (2-(2-(2-(tert-butyloxycarbonyl)aminoéthoxy)éthoxy)acétyl)-L-lysine, Nα -Fmoc- Nε - (AEEA-Boc) -L-Lysine
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$88.83 /25 mg
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Product Information

Fmoc-L-Lys(Boc-AEEA)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective deprotection of amines during solid-phase peptide synthesis. Its unique structure, incorporating a Boc (tert-butyloxycarbonyl) group and an ethylene glycol-based linker, enhances solubility and stability, making it an excellent choice for researchers focused on complex peptide sequences.

This compound is particularly beneficial in the design of peptide-based therapeutics and bioconjugates, where precise control over functional groups is essential. Its application extends to the development of targeted drug delivery systems and the synthesis of peptide mimetics, which can improve bioavailability and efficacy. Researchers in medicinal chemistry and biochemistry will find Fmoc-L-Lys(Boc-AEEA)-OH invaluable for advancing their projects, thanks to its favorable properties and adaptability in various synthetic pathways.

Synonyms
Nα -Fmoc- Nε- (2-(2-(2-(tert-butyloxycarbonyl)aminoéthoxy)éthoxy)acétyl)-L-lysine, Nα -Fmoc- Nε - (AEEA-Boc) -L-Lysine
CAS Number
1662688-16-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C32H43N3O9
Molecular Weight
613.7
MDL Number
MFCD27952843
PubChem ID
155885848
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = -9 ± 2 º (C=1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Nα -Fmoc- Nε- (2-(2-(2-(tert-butyloxycarbonyl)aminoéthoxy)éthoxy)acétyl)-L-lysine, Nα -Fmoc- Nε - (AEEA-Boc) -L-Lysine
CAS Number
1662688-16-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C32H43N3O9
Molecular Weight
613.7
MDL Number
MFCD27952843
PubChem ID
155885848
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = -9 ± 2 º (C=1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-Lys(Boc-AEEA)-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 structures for various applications in drug development.
  • Drug Delivery Systems: Its unique properties enable the formulation of advanced drug delivery systems, enhancing the bioavailability and targeted delivery of therapeutic agents.
  • Bioconjugation: The compound is effective in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, which is crucial in developing targeted therapies.
  • Research in Cancer Therapy: By enabling the design of peptide-based drugs, it plays a significant role in cancer research, helping to create more effective treatments with fewer side effects.
  • Protein Engineering: This chemical is also used in protein engineering, allowing scientists to modify proteins for improved stability and functionality in various biotechnological applications.

Citations