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Catalog Number:
36181
CAS Number:
68941-06-0
4′-Aminobenzo-18-couronne-6
Purity:
≥ 97% (CG)
Synonym(s):
(Benzo-18-couronne-6)-4'-ylamine
Documents
$97.40 /100 mg
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Product Information

4'-Aminobenzo-18-crown-6 is a versatile crown ether known for its ability to selectively complex with cations, particularly alkali and alkaline earth metals. This compound features a unique structure that enhances its solubility and binding properties, making it an invaluable tool in various fields such as analytical chemistry, organic synthesis, and materials science. Researchers utilize 4'-Aminobenzo-18-crown-6 for ion-selective electrodes, extraction processes, and as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions allows for precise applications in catalysis and sensor development, providing significant advantages over traditional ligands due to its enhanced selectivity and stability.

In addition to its analytical applications, 4'-Aminobenzo-18-crown-6 is also explored in drug delivery systems and supramolecular chemistry, where its ability to encapsulate guest molecules can lead to innovative therapeutic solutions. The compound's unique properties make it a preferred choice for researchers looking to develop new materials or improve existing methodologies in various chemical processes.

Synonyms
(Benzo-18-couronne-6)-4'-ylamine
CAS Number
68941-06-0
Purity
≥ 97% (CG)
Molecular Formula
C 16 H 256
Molecular Weight
327.37
MDL Number
MFCD00210009
PubChem ID
2724802
Appearance
Poudre blanche à beige à marron
Conditions
Magasin chez RT
General Information
Synonyms
(Benzo-18-couronne-6)-4'-ylamine
CAS Number
68941-06-0
Purity
≥ 97% (CG)
Molecular Formula
C 16 H 256
Molecular Weight
327.37
MDL Number
MFCD00210009
PubChem ID
2724802
Appearance
Poudre blanche à beige à marron
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4'-Aminobenzo-18-crown-6 is widely utilized in research focused on:

  • Selective Ion Binding: This compound is effective in selectively binding cations, particularly potassium ions, making it valuable in ion-selective electrodes used in analytical chemistry.
  • Drug Delivery Systems: Its ability to form complexes with various drugs enhances solubility and bioavailability, which is crucial in pharmaceutical applications for improving therapeutic efficacy.
  • Organic Synthesis: It serves as a reagent in organic synthesis, facilitating reactions that require specific ion coordination, thus streamlining the development of complex organic molecules.
  • Environmental Monitoring: The compound is used in sensors designed to detect heavy metal ions in environmental samples, aiding in pollution control and ensuring safety in water quality assessments.
  • Research in Supramolecular Chemistry: It plays a significant role in the study of supramolecular structures, contributing to advancements in materials science and nanotechnology.

Citations