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Catalog Number:
15085
CAS Number:
1049729-27-2
Chlorhydrate de fmoc-4-aminométhyl)pipéridine
Purity:
≥ 99 % (HPLC)
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Product Information

(Fmoc-4-aminomethyl)piperidine hydrochloride is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This compound serves as a protective group for amines, allowing for selective reactions in complex organic syntheses. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, provides stability during the synthesis process while enabling easy removal under mild conditions. Researchers appreciate its application in solid-phase peptide synthesis, where it facilitates the assembly of peptides with high purity and yield. Additionally, its role in drug discovery and development is significant, as it aids in the design of bioactive molecules by providing a functional handle for further modifications.

The compound's solubility in common organic solvents enhances its usability in various laboratory settings, making it a preferred choice among chemists. Its compatibility with diverse coupling reagents and its ability to form stable intermediates contribute to its effectiveness in synthesizing complex structures. Overall, (Fmoc-4-aminomethyl)piperidine hydrochloride stands out for its efficiency and reliability in advancing research and development in pharmaceutical applications.

CAS Number
1049729-27-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C21H24N2O2 · HCl
Molecular Weight
372.89
MDL Number
MFCD03093511
PubChem ID
2756220
Melting Point
> 121 ºC (déc.)
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1049729-27-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C21H24N2O2 · HCl
Molecular Weight
372.89
MDL Number
MFCD03093511
PubChem ID
2756220
Melting Point
> 121 ºC (déc.)
Appearance
Poudre cristalline 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-aminomethyl)piperidine hydrochloride 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 interfering with other functional groups. This is crucial in the pharmaceutical industry for developing new drugs.
  • Drug Development: Its role in modifying amino acids enhances the stability and bioavailability of therapeutic peptides, making it valuable in the creation of more effective medications.
  • Bioconjugation: The compound is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and targeted drug delivery systems.
  • Research in Neuroscience: It is utilized in the development of compounds that can interact with neurotransmitter systems, aiding in the study of neurological disorders and potential treatments.
  • Material Science: The compound can be incorporated into polymer systems to enhance properties such as solubility and thermal stability, which is beneficial in creating advanced materials for various applications.

Citations