28125
18-Crown-6
purum, ≥99.0% (GC)
Synonym(s):
18C6, 1,4,7,10,13,16-Hexaoxacyclooctadecane
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C12H24O6
CAS Number:
Molecular Weight:
264.32
Beilstein:
1619616
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
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
related product
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Effect of base-acid properties of the mixtures of water with methanol on the solution enthalpy of selected cyclic ethers in this mixture at 298.15 K.
Jozwiak M and Warczakowska A
Journal of Thermal Analysis and Calorimetry, 121(2), 765-770 (2015)
Chiral separations by host-guest complexation with cyclodextrin and crown ether in capillary zone electrophoresis.
Kuhn R, et al.
Chromatographia, 33(1-2), 32-36 (1992)
Separation of transition metal cations by capillary electrophoresis optimization of complexing agent concentrations (lactic acid and 18-crown-6).
Francois C, et al.
Journal of Chromatography A, 717(1-2), 393-408 (1995)
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.
de Namor AFD, et al.
Physical Chemistry Chemical Physics, 3(18), 4010-4021 (2001)
F. Vogtle et al.
Topics in Current Chemistry, 98 (1981)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service