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About This Item
Empirical Formula (Hill Notation):
C20H36O6
CAS Number:
Molecular Weight:
372.50
Beilstein:
1130529
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
98%
form
solid
functional group
ether
SMILES string
C1CCC2OCCOCCOC3CCCCC3OCCOCCOC2C1
InChI
1S/C20H36O6/c1-2-6-18-17(5-1)23-13-9-21-11-15-25-19-7-3-4-8-20(19)26-16-12-22-10-14-24-18/h17-20H,1-16H2
InChI key
BBGKDYHZQOSNMU-UHFFFAOYSA-N
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Application
Anion activator, and complexing agent which solubilizes alkali metal ions in non-polar solvents.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Giorgio Della Sala et al.
Organic & biomolecular chemistry, 11(5), 726-731 (2012-11-03)
The synthesis, complexation properties and catalytic activities under phase-transfer (PT) conditions of differently substituted cyclohexapeptoids are reported. Association constants, for small cationic alkali, and catalytic performances, in a model nucleophilic substitution, are comparable to those of representative crown ethers. Noteworthy
Aldrichimica Acta, 4, 1-1 (1971)
P Arhem et al.
Acta physiologica Scandinavica, 114(4), 593-600 (1982-04-01)
A potassium carrying ionophore dicyclohexano-18-crown-6 was found to affect the specific ionic currents in the node of Ranvier. Its presence caused an inactivation of the potassium permeability mechanism and a decrease of the sodium permeability. The rate of inactivation of
Aldrichimica Acta, 9, 3-3 (1976)
Radioiodination of alkyl halides with Na 125I catalyzed by dicyclohexyl-18-crown-6.
L Bo-Li et al.
Radioisotopes, 30(7), 391-393 (1981-07-01)
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