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Catalog Number:
05726
CAS Number:
159751-47-0
Fmoc-L-α-aminoadipic acid δ-tert-butyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Aad(OtBu)-OH, Fmoc-L-2-aminohexanedioic acid δ-tert-butyl ester
Documents
$127.79 /250MG
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Product Information

Fmoc-L-a-aminoadipic acid d-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This compound serves as a protective group for amino acids, facilitating the formation of peptide bonds while ensuring stability during various chemical reactions. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, allows for easy removal under mild conditions, making it an ideal choice for researchers aiming to streamline their synthesis processes.

In addition to its role in peptide synthesis, Fmoc-L-a-aminoadipic acid d-tert-butyl ester is also valuable in the development of bioactive compounds and drug candidates. Its ability to enhance solubility and stability of peptides can lead to improved pharmacological properties, making it a preferred choice in medicinal chemistry. Researchers in the fields of biochemistry and pharmaceutical sciences will find this compound particularly beneficial for creating complex peptide structures with high purity and yield.

Synonyms
Fmoc-L-Aad(OtBu)-OH, Fmoc-L-2-aminohexanedioic acid δ-tert-butyl ester
CAS Number
159751-47-0
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29NO6
Molecular Weight
439.4
MDL Number
MFCD00237006
PubChem ID
22314653
Appearance
White to off-white solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Aad(OtBu)-OH, Fmoc-L-2-aminohexanedioic acid δ-tert-butyl ester
CAS Number
159751-47-0
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29NO6
Molecular Weight
439.4
MDL Number
MFCD00237006
PubChem ID
22314653
Appearance
White to off-white solid
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-a-aminoadipic acid d-tert-butyl ester is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the efficient assembly of complex peptide sequences.
  • Drug Development: Its application in drug design helps create peptide-based therapeutics, which are crucial in treating various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The chemical is used for bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted drug delivery systems.
  • Research in Biochemistry: It plays a significant role in biochemical research, particularly in studying protein interactions and functions, aiding researchers in understanding cellular processes.
  • Modification of Amino Acids: This compound allows for the modification of amino acids, enhancing their properties for specific applications in both research and industrial settings, leading to more effective experimental outcomes.

Citations