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208019
Kaliumhexacyanoferrat(III)
99%
Synonym(e):
Kaliumferricyanid, Rotes Blutlaugensalz
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About This Item
Empfohlene Produkte
Assay
99%
SMILES String
[K+].[K+].[K+].N#C[Fe-3](C#N)(C#N)(C#N)(C#N)C#N
InChI
1S/6CN.Fe.3K/c6*1-2;;;;/q;;;;;;-3;3*+1
InChIKey
MIMJFNVDBPUTPB-UHFFFAOYSA-N
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Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Aquatic Chronic 2 - Eye Irrit. 2
Zusätzliche Gefahrenhinweise
Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 2
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves
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Environmental toxicology and chemistry, 30(5), 1013-1017 (2011-02-11)
The current study deals with the effect of humic substances (HS) on toxicity of solutions of a model inorganic oxidizer, potassium ferricyanide. Chemical reactions responsible for toxicity changes are under consideration. The bioluminescent system of coupled enzymatic reactions catalyzed by
Biomedical microdevices, 13(2), 279-289 (2010-11-26)
Microlithographically fabricated interdigitated microsensor electrodes (IMEs) were cleaned, surface activated, chemically functionalized (amine) and derivatized with an Acrloyl-PEG-NHS to receive a spun-applied monomer cocktail of UV polymerizable monomer. IMEs were 2050.5, 1550.5, 1050.5 and 0550.5 possessing lines and spaces that
Journal of pharmaceutical and biomedical analysis, 58, 141-145 (2011-10-15)
In this paper, a novel chemiluminescence (CL) system, 2-phenyl-4, 5-di (2-furyl) imidazole (PDFI)-potassium ferricyanide, for the determination of terbutaline sulfate was described. The method was based on enhancement of CL emission of PDFI-potassium ferricyanide system in the presence of terbutaline
ChemSusChem, 5(6), 1086-1091 (2012-05-10)
To scale-up microbial fuel cells (MFCs), installing multiple unit cells in a common reactor has been proposed; however, there has been a serious potential drop when connecting unit cells in series. To determine the source of the loss, a basic
Drug metabolism and disposition: the biological fate of chemicals, 39(6), 1022-1030 (2011-03-03)
Lapatinib, an oral breast cancer drug, has recently been reported to be a mechanism-based inactivator of cytochrome P450 (P450) 3A4 and also an idiosyncratic hepatotoxicant. It was suggested that formation of a reactive quinoneimine metabolite was involved in mechanism-based inactivation
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