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09877

Sigma-Aldrich

Ammonium ionophore I

Selectophore, function tested, ≥98.0% ((Total homologs), HPLC)

Synonym(s):

Nonactin, Ammonium ionophore

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About This Item

Empirical Formula (Hill Notation):
C40H64O12
CAS Number:
Molecular Weight:
736.93
Beilstein/REAXYS Number:
76434
EC Number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NB.61

grade

for ion-selective electrodes

Quality Level

product line

Selectophore

assay

≥98.0% ((Total homologs), HPLC)

form

powder

quality

function tested

storage temp.

2-8°C

SMILES string

C[C@H]1C[C@@H]2CC[C@@H](O2)[C@@H](C)C(=O)O[C@H](C)C[C@H]3CC[C@H](O3)[C@H](C)C(=O)O[C@@H](C)C[C@@H]4CC[C@@H](O4)[C@@H](C)C(=O)O[C@H](C)C[C@H]5CC[C@H](O5)[C@H](C)C(=O)O1

InChI

1S/C40H64O12/c1-21-17-29-9-13-34(49-29)26(6)38(42)46-23(3)19-31-11-15-36(51-31)28(8)40(44)48-24(4)20-32-12-16-35(52-32)27(7)39(43)47-22(2)18-30-10-14-33(50-30)25(5)37(41)45-21/h21-36H,9-20H2,1-8H3/t21-,22+,23+,24-,25-,26+,27+,28-,29-,30+,31+,32-,33-,34+,35+,36-

InChI key

RMIXHJPMNBXMBU-QIIXEHPYSA-N

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General description

Purified for use in ion-selective electrodes
Visit our Sensor Applications portal to learn more.

Application

Selected application examples
Determination of potassium ions in pharmaceutical samples by FIA using a potentiometric electrode based on ionophore nonactin occluded in EVA membrane.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Transports alkali cations through biological membranes, with high selectivity for ammonia.

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Y.M. Fraticelli, M.E. Meyerhoff
Analytical Chemistry, 53, 1857-1861 (1981)
The kinetic and equilibrium components of selective ionic permeability mediated by nactin- and valinomycin-type carriers having systematically varied degrees of methylation.
G Eisenman et al.
Annals of the New York Academy of Sciences, 264, 34-60 (1975-12-30)
D. Ammann et al.
Ion-Selective Rev., 5, 3-3 (1983)
Simon, W.
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 25, 811-811 (1971)
Brian R Kusche et al.
Bioorganic & medicinal chemistry letters, 19(4), 1233-1235 (2009-01-27)
Nonactin, produced by Streptomyces griseus ETH A7796, is a macrotetrolide assembled from nonactic acid. It is an effective inhibitor of drug efflux in multidrug resistant erythroleukemia K562 cells at sub-toxic concentrations and has been shown to possess both antibacterial and

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