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Merck

60299

Sigma-Aldrich

六氰基铁(III)酸钾

BioUltra, ≥99.0% (RT)

别名:

赤血盐, 铁氰化钾

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About This Item

线性分子式:
K3Fe(CN)6
CAS号:
分子量:
329.24
EC號碼:
MDL號碼:
分類程式碼代碼:
12171602
PubChem物質ID:
NACRES:
NA.25

等級

reagent grade

產品線

BioUltra

化驗

≥99.0% (RT)

形狀

crystals

雜質

insoluble matter, passes filter test

pH值

6-9 (25 °C, 1 M in H2O)

溶解度

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

負離子痕跡

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

正離子痕跡

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

吸收

no transmittance (UV) in H2O at 1 M

SMILES 字串

[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 密鑰

MIMJFNVDBPUTPB-UHFFFAOYSA-N

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應用

在流动注射化学发光和激光诱导荧光等检测系统中,六氰合铁酸钾 (Ⅲ)(红普鲁士酸)可作为电子受体。

其他說明

电子受体,用于涉及电子传递的系统,例如 NADH-细胞色素 b 5 还原酶 ;复合物 I 的含量测定

象形圖

Exclamation markEnvironment

訊號詞

Warning

危險聲明

危險分類

Aquatic Chronic 2 - Eye Irrit. 2

安全危害

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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