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49902

Supelco

Tin(II) ionophore I

Selectophore™

Sinonimo/i:

Dibenzo-18-crown-6, 2,3,11,12-Dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-diene, 6,7,9,10,17,18,20,21-Octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecene, DB18C6

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About This Item

Formula empirica (notazione di Hill):
C20H24O6
Numero CAS:
14187-32-7
Peso molecolare:
360.40
Beilstein:
1162153
Numero CE:
238-041-3
Numero MDL:
MFCD00005098
Codice UNSPSC:
26111700
ID PubChem:
329757542

Nome Commerciale

Selectophore™

Punto di fusione

162-164 °C (lit.)

Stringa SMILE

C1COc2ccccc2OCCOCCOc3ccccc3OCCO1

InChI

1S/C20H24O6/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/h1-8H,9-16H2
YSSSPARMOAYJTE-UHFFFAOYSA-N

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Descrizione generale

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Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Note legali

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number

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A Carabez et al.
Biochimica et biophysica acta, 638(1), 125-131 (1981-11-12)
In rat liver mitochondria, the macrocyclic polyether, dibenzo-18-crown-6 (polyether XXVIII) inhibits the oxidation of NAD-dependent substrates, as stimulated by ADP, uncouplers and valinomycin plus K+. It does not inhibit the oxidation of succinate. It is concluded that polyether XXVIII inhibits
Ying Han et al.
The Journal of organic chemistry, 77(5), 2422-2430 (2012-02-11)
A new triptycene-derived macrotricyclic host containing two dibenzo-[18]-crown-6 moieties was synthesized and shown to form 1:1 complexes with paraquat derivatives in solution, in which the guests all thread the central cavity of the host. However, it was interestingly found that
Design of ionophore hapten conjugates for electroimmunoassay.
G R Connell et al.
Proceedings of the Western Pharmacology Society, 27, 337-340 (1984-01-01)
Yuchuan Cheng et al.
Journal of colloid and interface science, 307(2), 447-454 (2007-01-09)
Reported here is the study on the structure of Langmuir-Blodgett (LB) films of double-armed dibenzo-18-crown-6 contain biphenyl (DACE) which are newly synthesized and mixed with stearic acid (SA). In addition, the miscibility of the two compounds was also tested by
L A Shahada
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(8), 1795-1798 (2005-05-03)
The interaction of the crown ether dibenzo-18-crown-6 (DBC) with iodine has been studied in CHCl3 at room temperature. The charge-transfer absorptions, far infrared and thermal measurements of the formed charge-transfer complex were recorded and discussed. The results obtained show the
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