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60299

Sigma-Aldrich

Potassium hexacyanoferrate(III)

BioUltra, ≥99.0% (RT)

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:
MDL number:
UNSPSC Code:
12171602
PubChem Substance ID:
NACRES:
NA.25

product line

BioUltra

Quality Level

Assay

≥99.0% (RT)

form

crystals

impurities

insoluble matter, passes filter test

pH

6-9 (25 °C, 1 M in H2O)

solubility

H2O: 1 M at 20 °C, clear, very strong brownish-yellow

anion traces

chloride (Cl-): ≤50 mg/kg
hexacyanoferrate(II) ([Fe(CN)6]4-): ≤200 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

As: ≤0.1 mg/kg
Ca: ≤5 mg/kg
Cd: ≤5 mg/kg
Co: ≤50 mg/kg
Cr: ≤50 mg/kg
Cu: ≤10 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤200 mg/kg
Ni: ≤10 mg/kg
Pb: ≤20 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

absorption

no transmittance (UV) in H2O at 1 M

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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Application

Potassium hexacyanoferrate(III) (red prussiate) may be used as an electron acceptor in detection systems such as flow injection chemiluminescence and laser-induced fluorescence.

Other Notes

Electron acceptor, employed in systems involving electron transport, e.g. NADH-cytochrome b5 reductase; assay of complex I

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2

Supplementary Hazards

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Incorporation of microsomal electron-transfer components into liposomes: considerations for diffusion-limited reactions.
P Strittmatter et al.
Methods in enzymology, 52, 206-211 (1978-01-01)
Detergent-solubilized NADH-cytochrome b5 reductase.
K Mihara et al.
Methods in enzymology, 52, 102-108 (1978-01-01)
Preparation and properties of NADH: ubiquinone oxidoreductase (complexI), EC 1.6.5.3.
Y Hatefi
Methods in enzymology, 53, 11-14 (1978-01-01)
Soichiro Ijiri et al.
Journal of chromatography. A, 1217(18), 3161-3166 (2010-03-23)
Rhodamine 110 (Rho110) has been used in the highly sensitive analysis of monosaccharides, as it reacts with the reducing carbonyl group of the saccharides. The monosaccharide derivatives were investigated by capillary electrophoresis with laser-induced fluorescence detection. The derivatization was performed
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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