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Catalog Number:
46523
CAS Number:
496946-83-9
Fmoc-N-Me-EDA(N'-Me)·HCl
Purity:
≥ 97% (HPLC)
Documents
$105.00 /100MG
Pack Size Availability Price
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Product Information

Fmoc-N-Me-EDA(N'-Me)·HCl is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, incorporating N-methyl and ethylene diamine functionalities, enhances its reactivity and compatibility with various coupling agents, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active molecules.

In addition to its application in peptide synthesis, Fmoc-N-Me-EDA(N'-Me)·HCl is also valuable in medicinal chemistry for the development of novel therapeutic agents. Its ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions makes it a preferred choice among professionals in pharmaceutical research. The compound's hydrochloride form ensures improved solubility, further enhancing its usability in laboratory settings. With its robust performance and adaptability, Fmoc-N-Me-EDA(N'-Me)·HCl stands out as a key reagent for advancing research in peptide-based therapeutics.

CAS Number
496946-83-9
Purity
≥ 97% (HPLC)
Molecular Formula
C19H23ClN2O2
Molecular Weight
346.86
MDL Number
MFCD30723357
PubChem ID
69756197
Appearance
Off-white to white solid
Conditions
Store at 0 - 8 °C
General Information
CAS Number
496946-83-9
Purity
≥ 97% (HPLC)
Molecular Formula
C19H23ClN2O2
Molecular Weight
346.86
MDL Number
MFCD30723357
PubChem ID
69756197
Appearance
Off-white to white solid
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-N-Me-EDA(N'-Me)·HCl 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 while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, particularly in creating compounds with improved stability and bioavailability.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and drug delivery systems.
  • Research in Neuroscience: It aids in the synthesis of neuropeptides, which are vital for studying neuronal signaling and developing treatments for neurological disorders.
  • Custom Chemical Synthesis: Researchers leverage its unique properties for creating tailored compounds in various fields, including materials science and nanotechnology, offering versatility compared to other protective groups.

Citations