28125
18-Crown-6
purum, ≥99.0% (GC)
Synonym(s):
18C6, 1,4,7,10,13,16-Hexaoxacyclooctadecane
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About This Item
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grade
purum
Quality Level
assay
≥99.0% (GC)
form
solid
mp
38-41 °C
42-45 °C (lit.)
SMILES string
O1CCOCCOCCOCCOCCOCC1
InChI
1S/C12H24O6/c1-2-14-5-6-16-9-10-18-12-11-17-8-7-15-4-3-13-1/h1-12H2
InChI key
XEZNGIUYQVAUSS-UHFFFAOYSA-N
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Application
18-Crown-6 can be used as a model for crown ethers to study the effect of acid-base properties of mixed solvent on their solution enthalpy.It is generally used as a phase transfer catalyst and a complexing agent. It specifically binds to potassium ion, ammonium or protonated alkyl amines to form complexes.
Can be useful as phase-transfer catalysts.
Other Notes
Macrocyclic polyethers with repeating (-CH2CH2O) units. The compounds are ionophoric (form stable complexes with cations).
Phase transfer catalyst, complexing-agent
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Description
Pricing
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Topics in Current Chemistry, 98 (1981)
Lower rim calix (4) arene ketone derivatives and their interaction with alkali metal cations. Structural and thermodynamic (solution and complexation) characterisation of the tetraphenyl ketone derivative and its sodium complex.
Physical Chemistry Chemical Physics, 3(18), 4010-4021 (2001)
Counter cation-controlled air oxidation of manganese derivatives of tetrachlorocatechol.
Inorganic Chemistry Communications, 3(2), 76-79 (2000)
Separation of transition metal cations by capillary electrophoresis optimization of complexing agent concentrations (lactic acid and 18-crown-6).
Journal of Chromatography A, 717(1-2), 393-408 (1995)
Chiral separations by host-guest complexation with cyclodextrin and crown ether in capillary zone electrophoresis.
Chromatographia, 33(1-2), 32-36 (1992)
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