Bis (3,4-dibromobenzene) -18-crown-6

98%

  • Product Code: 51442
  CAS:    40100-11-6
Molecular Weight: 675.9852 g./mol Molecular Formula: C₂₀H₂₀Br₄O₆
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily utilized in the field of supramolecular chemistry due to its crown ether structure, which enables it to selectively bind with specific ions or molecules. Its unique ability to form stable complexes with cations, particularly potassium ions, makes it valuable in ion transport studies and membrane separation processes. Additionally, it is employed in the development of sensors and molecular recognition systems, where its selective binding properties enhance detection accuracy. The bromine atoms in its structure also contribute to its use in flame retardant applications, where it can be incorporated into polymers to improve fire resistance. Furthermore, its role in catalysis and as a phase transfer catalyst in organic synthesis highlights its versatility in facilitating chemical reactions.
Product Specification:
Test Specification
APPEARANCE White powder
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $70.51
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0.500 10-20 days $214.52
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1.000 10-20 days $330.03
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Bis (3,4-dibromobenzene) -18-crown-6
This chemical is primarily utilized in the field of supramolecular chemistry due to its crown ether structure, which enables it to selectively bind with specific ions or molecules. Its unique ability to form stable complexes with cations, particularly potassium ions, makes it valuable in ion transport studies and membrane separation processes. Additionally, it is employed in the development of sensors and molecular recognition systems, where its selective binding properties enhance detection accuracy. The bromine atoms in its structure also contribute to its use in flame retardant applications, where it can be incorporated into polymers to improve fire resistance. Furthermore, its role in catalysis and as a phase transfer catalyst in organic synthesis highlights its versatility in facilitating chemical reactions.
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