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1,3 Di-n-Octyloxycalix (4) arene crown-6
1,3 Di-n-Octyloxycalix (4) arene crown-6

1,3 Di-n-Octyloxycalix (4) arene crown-6

MOQ : 1 Kilogram

1,3 Di-n-Octyloxycalix (4) arene crown-6 Specification

  • Storage Instructions
  • Store in a cool, dry place, protected from light
  • Shelf Life
  • 24 months from manufacturing date
  • Size
  • Custom packaging, typically 1g, 5g, or 10g
  • Physical State
  • Solid
  • Melting Point
  • 230-235C
  • Boiling point
  • Not available (decomposes)
  • Packaging Type
  • Sealed bottle
  • Molecular Formula
  • C64H104O8
  • Molecular Weight
  • 1036.46 g/mol
  • Usage
  • Research and development
  • Ph Level
  • Neutral (at standard conditions)
  • Purity
  • >98%
  • Density
  • 1.07 Gram per cubic centimeter(g/cm3)
  • CAS No
  • 121579-07-9
  • Grade
  • Laboratory Reagent
  • Type
  • Calixarene Crown Ether
  • Application
  • Supramolecular chemistry, cation binding, sensor research
  • Appearance
  • White to off-white solid
  • Purity(%)
  • >98%
 

1,3 Di-n-Octyloxycalix (4) arene crown-6 Trade Information

  • Minimum Order Quantity
  • 1 Kilogram
  • Supply Ability
  • 1 Kilogram Per Week
  • Delivery Time
  • 1 Week
 

About 1,3 Di-n-Octyloxycalix (4) arene crown-6

1,3 Di-n-octyloxy Calix[4]arene crown-6

Product

 1,3 Di-n-octyloxy Calix[4]arene crown-6

CAS Number

161282-97-9

Molecular Formula

C54H74O8

Business

Manufacturers & Exporters of 1,3 Di-n-octyloxy Calix[4]arene crown-6 from India.


Test Parameters

Specifications

Molecular Weight

851.17

Appearance

White colour crystalline powder.

Melting Point in degree Centigrade

94-98°C

Purity

98% Purity by HPLC

1,3 dioctyloxy calix-4-arene crown-6:

1,3 dioctyloxy calix-4-arene crown-6 is a calixarene with aliphatic ether alcohol function group appended to the lower rim and a crown cap forming a crown ether. This calix crown ether could be potentially used in nuclear waste management. 1,3 dioctyloxy calix-4-arene crown-6.





Comprehensive Applications in Research

This reagent is widely used in advanced cation binding studies and plays a significant role in supramolecular chemistry and sensor development. Its high selectivity in complexation makes it invaluable for scientists exploring molecular recognition or crafting sensitive detection systems. With its stability and purity, the compound supports innovative research directions in academic and industrial laboratories.


Quality Assured Synthesis and Packaging

Produced through meticulous synthetic processes and column purification, the calix[4]arene crown-6 derivative ensures a purity greater than 98%. It is packed in sealed bottles to maintain stability, typically available in 1g, 5g, or 10g sizes. Custom packaging can be arranged. The shelf life extends up to 24 months when stored in a cool, dry place protected from light.

FAQs of 1,3 Di-n-Octyloxycalix (4) arene crown-6:


Q: How should 1,3-Di-n-Octyloxycalix(4)arene crown-6 be stored to ensure maximum stability?

A: Store the compound in a cool, dry place away from direct light. Sealed packaging helps protect the product, and it remains stable for up to 24 months under these recommended storage conditions.

Q: What are the main uses of this compound in scientific research?

A: This compound is extensively utilized in supramolecular chemistry, cation binding studies, and the development of chemical sensors, thanks to its crown-6 ether moietys exceptional ion-binding capacity.

Q: When is it appropriate to choose this calix[4]arene derivative over other crown ethers?

A: Select 1,3-Di-n-Octyloxycalix(4)arene crown-6 when a high degree of selectivity in cation binding or complex molecular recognition is required, as its structure offers advantages in these areas over standard crown ethers.

Q: Where can this laboratory reagent be sourced and in what quantities?

A: It is available through distributors, exporters, importers, manufacturers, suppliers, traders, and wholesalers in India, and can typically be ordered in 1g, 5g, or 10g quantities with custom options on request.

Q: What is the recommended process for using the compound in experimental protocols?

A: Dissolve the solid in appropriate organic solvents such as chloroform or dichloromethane to create a working solution, following standard laboratory handling and measuring techniques.

Q: What are the benefits of using this specific calixarene crown ether in research applications?

A: Researchers benefit from its high chemical purity, selective cation binding abilities, structural stability, and ease of handling, all of which enhance experimental accuracy and reliability.

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