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Catalog Number:
46557
Ester δ-tert-butylique de l'acide Fmoc-D-α-aminoadipique
Purity:
≥ 99 % (HPLC chirale)
Synonym(s):
Fmoc-D-Aad(OtBu)-OH, Ester δ-tert-butylique de l'acide Fmoc-D-2-aminohexanedioïque
Temperature Sensitive
Documents
$210.00 /100 mg
Taille
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Product Information

Fmoc-D-a-aminoadipic acid d-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis process. Its d-tert-butyl ester form enhances solubility and stability, making it an ideal choice for researchers working in organic chemistry and biochemistry. The compound is particularly valuable in the production of peptides that require specific stereochemistry, allowing for the creation of biologically active molecules with tailored properties.

In practical applications, Fmoc-D-a-aminoadipic acid d-tert-butyl ester is employed in the synthesis of peptide-based therapeutics, where precision in amino acid configuration is crucial. Its unique structure allows for efficient coupling reactions, significantly improving yields and purity in peptide synthesis. Researchers benefit from its compatibility with various coupling reagents and its ability to undergo deprotection under mild conditions, making it a reliable choice for both academic and industrial applications.

Synonyms
Fmoc-D-Aad(OtBu)-OH, Ester δ-tert-butylique de l'acide Fmoc-D-2-aminohexanedioïque
Purity
≥ 99 % (HPLC chirale)
Molecular Formula
C 25 H 296
Molecular Weight
439.5
Appearance
Solide blanc
Conditions
Conserver à ≤ - 4 °C
General Information
Synonyms
Fmoc-D-Aad(OtBu)-OH, Ester δ-tert-butylique de l'acide Fmoc-D-2-aminohexanedioïque
Purity
≥ 99 % (HPLC chirale)
Molecular Formula
C 25 H 296
Molecular Weight
439.5
Appearance
Solide blanc
Conditions
Conserver à ≤ - 4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-D-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, allowing researchers to create complex structures for drug development and biological studies.
  • Bioconjugation: It is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Drug Development: The compound plays a significant role in the pharmaceutical industry, particularly in the design of novel therapeutics that target specific diseases.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, aiding in the understanding of neurological disorders and potential treatments.
  • Material Science: This chemical is also applied in the development of advanced materials, contributing to the creation of polymers with unique properties for various industrial applications.

Citations