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Catalog Number:
29659
S-Fmoc-2-amino-6-tert-butoxycarbonyl-heptanedioic acid -7-tert-butyl ester
Purity:
≥ 98% (HPLC)
Documents
$141.41 /25MG
Pack Size Availability Price
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Product Information

(S)-Fmoc-2-amino-6-tert-butoxycarbonyl-heptanedioic acid -7-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which facilitates the selective coupling of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the tert-butoxycarbonyl (Boc) and tert-butyl ester functionalities, enhances stability and solubility, making it an ideal choice for researchers aiming to optimize their synthetic routes.

In the pharmaceutical industry, this compound plays a crucial role in the development of bioactive peptides, which are essential for therapeutic applications. Its ability to protect functional groups while allowing for further modifications makes it invaluable in creating complex peptide libraries. Researchers benefit from its high purity and reliable performance, ensuring consistent results in their experiments. With its significant applications in medicinal chemistry and biochemistry, (S)-Fmoc-2-amino-6-tert-butoxycarbonyl-heptanedioic acid -7-tert-butyl ester stands out as a key reagent for advancing peptide-based research and development.

Purity
≥ 98% (HPLC)
Molecular Formula
C31H39NO8
Molecular Weight
553.65
MDL Number
MFCD18782833
Appearance
White powder
Optical Rotation
- 8 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Purity
≥ 98% (HPLC)
Molecular Formula
C31H39NO8
Molecular Weight
553.65
MDL Number
MFCD18782833
Appearance
White powder
Optical Rotation
- 8 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-2-amino-6-tert-butoxycarbonyl-heptanedioic acid -7-tert-butyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without affecting other functional groups. Its stability under various conditions makes it a preferred choice in complex peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates by modifying amino acids, enhancing bioavailability and therapeutic efficacy. This is particularly important in designing targeted therapies.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to therapeutic agents. This application is crucial in developing targeted delivery systems in cancer therapy.
  • Material Science: It finds applications in creating functionalized polymers, which can be used in drug delivery systems and biomaterials, improving the performance and compatibility of materials in medical devices.
  • Research in Biochemistry: The compound is valuable in biochemical studies, particularly in understanding protein interactions and enzyme mechanisms, providing insights that can lead to breakthroughs in various biological processes.

Citations