208019
Potassium hexacyanoferrate(III)
99%
Synonym(s):
Potassium ferricyanide, Red prussiate
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About This Item
Linear Formula:
K3Fe(CN)6
CAS Number:
Molecular Weight:
329.24
EC Number:
237-323-3
UNSPSC Code:
12352103
MDL number:
InChI key
MIMJFNVDBPUTPB-UHFFFAOYSA-N
InChI
1S/6CN.Fe.3K/c6*1-2;;;;/q;;;;;;-3;3*+1
SMILES string
[K+].[K+].[K+].N#C[Fe-3](C#N)(C#N)(C#N)(C#N)C#N
assay
99%
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2
supp_hazards
Storage Class
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Liju Yang et al.
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
Daehee Kim et al.
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
Lu Han et al.
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
Suqin Han et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(28), 2901-2904 (2010-09-08)
A novel capillary electrophoresis (CE) with chemiluminescence (CL) detection method for the determination of mitoxantrone (MTX) has been developed, which based on the CL reaction of potassium ferricyanide with luminol in sodium hydroxide medium sensitized by MTX. Under optimum analytical
Hideo Takakusa et al.
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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