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455946

Sigma-Aldrich

六氰基铁(III)酸钾

99.98% trace metals basis

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:
13746-66-2
分子量:
329.24
EC號碼:
237-323-3
MDL號碼:
MFCD00011392
分類程式碼代碼:
12352302
PubChem物質ID:
24869096
NACRES:
NA.23

等級

for analytical purposes

品質等級

100

化驗

99.98% trace metals basis

形狀

crystalline

雜質

≤250.0 ppm Trace Metal Analysis

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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相关类别

應用

铁氰化钾掺杂剂可用于将 Li4Ti5O12（LTO）与 K 和 Fe 共掺杂，使得 LTO 作为锂离子电池的阳极时具有更良好的电化学性能。

象形圖

Exclamation markEnvironment
GHS07,GHS09

訊號詞

Warning

危險聲明

H319,H411

危險分類

Aquatic Chronic 2 - Eye Irrit. 2

安全危害

EUH032

儲存類別代碼

11 - 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
MKCL7806
MKCJ5574
MKCF8792
MKCD4921
MKCC8515

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Using potassium ferricyanide as a dopant to prepare K and Fe co-doped Li4Ti5O12
Ding K, et al.
Ceramics International, 42.16, 19187-19194 (2016)
Effects of cathodic electron acceptors and potassium ferricyanide concentrations on the performance of microbial fuel cell
Wei L, et al.
International Journal of Hydrogen Energy, 37.17, 12980-12986 (2012)
Holger Schulze et al.
Sensors (Basel, Switzerland), 21(5) (2021-04-04)
Rapid point of care tests for bacterial infection diagnosis are of great importance to reduce the misuse of antibiotics and burden of antimicrobial resistance. Here, we have successfully combined a new class of non-biological binder molecules with electrochemical impedance spectroscopy
Sveinung Lillehaug et al.
Scientific data, 6, 190028-190028 (2019-02-27)
The spatial pattern of transgene expression in tetracycline-controlled mouse models is governed primarily by the driver line used to introduce the tetracycline-controlled transactivator (tTA). Detailed maps showing where each tTA driver activates expression are therefore essential for designing and using
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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