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Merck
모든 사진(1)

주요 문서

60299

Sigma-Aldrich

Potassium hexacyanoferrate(III)

BioUltra, ≥99.0% (RT)

동의어(들):

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 코드:
12171602
PubChem Substance ID:
NACRES:
NA.25
solubility:
H2O: 1 M at 20 °C, clear, very strong brownish-yellow

Grade

reagent grade

제품 라인

BioUltra

분석

≥99.0% (RT)

양식

crystals

불순물

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

음이온 미량물

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

양이온 미량물

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

흡수

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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애플리케이션

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

기타 정보

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

픽토그램

Exclamation markEnvironment

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2

보충제 위험성

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves


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문서 라이브러리 방문

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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