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158402

Sigma-Aldrich

Dicyclohexano-18-crown-6

98%

Synonym(s):

2,3,11,12-Dicyclohexano-1,4,7,10,13,16-hexaoxacyclooctadecane, 2,5,8,15,18,21-Hexaoxatricyclo[20.4.0.09.14]hexacosane, Dicyclohexyl-18-crown-6, Perhydro-dibenzo-18-crown-6

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1 G
¥3,750
10 G
¥35,700
100 G
¥229,000

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1 G
¥3,750
10 G
¥35,700
100 G
¥229,000

About This Item

Empirical Formula (Hill Notation):
C20H36O6
CAS Number:
16069-36-6
Molecular Weight:
372.50
Beilstein:
1130529
EC Number:
240-216-4
MDL number:
MFCD00005099
UNSPSC Code:
12352302
PubChem Substance ID:
24849733
NACRES:
NA.22

¥3,750

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Quality Level

200

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,[1] and complexing agent which solubilizes alkali metal ions in non-polar solvents.[2][3]

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H319

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

158402-1G:
158402-BULK:
158402-10G:
158402-VAR:
158402-100G:
158402-500G:
158402-2.5G:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP7143
SHBM3571
SHBM6110
SHBM3173
SHBK2833

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18-Crown-6 99%

Sigma-Aldrich

186651

18-Crown-6

Negar Bahraini et al.
Health physics, 101(2), 128-135 (2011-06-29)
A molecularly imprinted polymer (MIP) comprising dicyclohexano-18-crown-6 (DCH18C6) was synthesized as a Sr-selective sorbent for urine bioassay purposes. MIP particles (326 ± 2 nm diameter) were formed using acetone and acetonitrile (1:3 v/v) as the porogen, methacrylic acid (MAA) as
Gazzetta Chimica Italiana, 123, 19-19 (1993)
E W Bethge et al.
General physiology and biophysics, 10(3), 225-244 (1991-06-01)
The effects of some potassium channel blockers on the ionic currents and on the so-called K(+)-depolarization in intact myelinated nerve fibres were studied. 4-AP, and in particular, Flaxedil, proved to be selective K(+)-current blockers. However, TEA, a crown ether (DCH18C6)
Svetlana V Smirnova et al.
Analytical and bioanalytical chemistry, 378(5), 1369-1375 (2004-01-30)
Amino acids Trp, Gly, Ala, Leu are extracted efficiently from aqueous solution at pH 1.5-4.0 (Lys and Arg at pH 1.5-5.5) into the room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF(6)) with dicyclohexano-18-crown-6 (CE). The most hydrophilic amino acids such as
Camiel H C Janssen et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 15(16), 3536-3543 (2014-08-27)
The selective extraction of metals from aqueous mixtures has generally relied on the use of selective ionophores. We present an alternative strategy that exploits a recently developed approach to extraction into an ionic liquid phase, and show that a high
View All Related Papers

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