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Sigma-Aldrich

Potassium hexacyanoferrate(III)

ACS reagent, ≥99.0%

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Synonym(s):
Potassium ferricyanide, Red prussiate
Linear Formula:
K3Fe(CN)6
CAS Number:
Molecular Weight:
329.24
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

Assay

≥99.0%

form

powder or crystals

reaction suitability

reagent type: catalyst
core: iron

impurities

≤0.005% insolubles

pH

6-9 (25 °C, 329 g/L)

anion traces

chloride (Cl-): ≤0.01%
sulfate (SO42-): ≤0.01%

cation traces

Fe: ≤0.05%

storage temp.

room temp

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

InChI key

MIMJFNVDBPUTPB-UHFFFAOYSA-N

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General description

Potassium hexacyanoferrate(III) (Potassium ferricyanide) can be prepared by the anodic oxidation of K4[Fe(CN)6].

Application

Potassium hexacyanoferrate(III) [Potassium ferricyanide] has been used as an oxidant in the preparation of diethidium and di-mito-ethidium. It reacts with cobalt chloride hexahydrate to afford CoHCF (Cobalt hexacyanoferrate) nanoparticles.
It may be employed as an oxidizing agent during the fabrication of glucose conductometric biosensor.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2

Supplementary Hazards

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Eagleson M.
Concise Encyclopedia Chemistry, 291-291 (1994)
Glucose conductometric biosensor with potassium hexacyanoferrate (III) as an oxidizing agent.
Dzyadevich SV, et al.
Analytica Chimica Acta, 374(1), 11-18 (1998)
Macro-micro relationship in nanostructured functional
Composites
Zanotto A, et al.
Express Polymer Letters, 6(5), 410-416 (2012)
Thorsten Litzenburger et al.
Clinical science (London, England : 1979), 134(7), 921-939 (2020-04-03)
Maternal obesity determines obesity and metabolic diseases in the offspring. The white adipose tissue (WAT) orchestrates metabolic pathways, and its dysfunction contributes to metabolic disorders in a sex-dependent manner. Here, we tested if sex differences influence the molecular mechanisms of
Jacek Zielonka et al.
Free radical biology & medicine, 46(3), 329-338 (2008-11-26)
Methods for the detection and quantitation of hydroethidine (HE) and its oxidation products by HPLC analysis are described. Synthetic methods for preparation of authentic standards (2-hydroxyethidium and diethidium) are provided. Potential applications of the HPLC methods to chemical and biological

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