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Catalog Number:
15054
CAS Number:
221352-82-5
Fmoc-4-amino-1-carboxyméthylpipéridine
Purity:
≥ 97 % (HPLC)
Documents
$120.88 /250 mg
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Product Information

Fmoc-4-amino-1-carboxymethylpiperidine is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The compound's stability under various reaction conditions enhances its applicability in both academic and industrial settings, particularly in the pharmaceutical sector where precision and reliability are paramount.

In addition to its role in peptide synthesis, Fmoc-4-amino-1-carboxymethylpiperidine serves as a valuable intermediate in the development of bioactive compounds. Its ability to facilitate the introduction of functional groups makes it a key player in the design of novel therapeutics. Researchers have leveraged this compound in studies aimed at understanding protein interactions and developing targeted drug delivery systems. With its proven track record and robust performance, Fmoc-4-amino-1-carboxymethylpiperidine stands out as a critical reagent for professionals seeking to innovate in the fields of biochemistry and pharmacology.

CAS Number
221352-82-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H24N2O4
Molecular Weight
380.51
MDL Number
MFCD01321021
PubChem ID
2756150
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
221352-82-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H24N2O4
Molecular Weight
380.51
MDL Number
MFCD01321021
PubChem ID
2756150
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-4-amino-1-carboxymethylpiperidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based pharmaceuticals, enhancing the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: Researchers use it to facilitate the conjugation of peptides to various biomolecules, improving the efficacy of drug delivery systems.
  • Research in Neuroscience: Its derivatives are explored in studies related to neuropeptides, aiding in the understanding of neurological pathways and potential treatments for disorders.
  • Material Science: The compound is applied in the development of functionalized materials, contributing to advancements in nanotechnology and biomaterials.

Citations