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Sigma-Aldrich

Iron(II) chloride

AnhydroBeads, −10 mesh, 99.99% trace metals basis

Synonym(s):

Ferrous chloride, Iron dichloride

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About This Item

Linear Formula:
FeCl2
CAS Number:
Molecular Weight:
126.75
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

product line

AnhydroBeads

Quality Level

assay

99.99% trace metals basis

impurities

≤150.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

677 °C (lit.)

density

3.16 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

Cl[Fe]Cl

InChI

1S/2ClH.Fe/h2*1H;/q;;+2/p-2

InChI key

NMCUIPGRVMDVDB-UHFFFAOYSA-L

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General description

Iron(II) chloride, also known as ferrous chloride, is a paramagnetic solid with a high melting point. It has significant applications in solar cells, fuel cell catalysts, and semiconductors due to its unique properties. Additionally, it can also act as a reducing agent in redox reactions, which are crucial in many electrochemical processes.

Application

Iron(II) chloride can be used as:      
  • A doping agent in the fabrication of mixed organic-inorganic perovskite for high-efficiency perovskite solar cells. The incorporation of iron(II) chloride improve the overall efficiency of the solar cell.     
  • A precursor for synthesizing various iron(II) coordination complexes. These complexes are significant due to their unique optical and electronic properties, which are essential for various applications, including solar energy conversion and catalysis.     
  • As a precursor in the synthesis of iron-nitrogen-carbon (Fe–N–C) catalysts for proton exchange membrane fuel cells.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

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Danger

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Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

8B - Non-combustible corrosive hazardous materials

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WGK 1

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does not flash

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does not flash

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Inorganic Chemistry, 37, 612-612 (1998)
Jiangfei Meng et al.
Journal of food science, 77(1), C8-14 (2011-12-21)
Wines made from 3 spine grape (Vitis davidii Foex) genotypes-Junzi 1# (JZ 1#), Junzi 2# (JZ 2#), and Liantang (LT)-and Cherokee rose (Rosa laevigata Michx., CR) were evaluated for their phenolics composition and antioxidant activities by several assays, including 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonic
Qinqin Xia et al.
The Journal of organic chemistry, 77(20), 9366-9373 (2012-10-03)
Iron-catalyzed direct C-N bond formation between azoles and amides is described. The oxidative coupling reactions of sp(3) C-H bonds adjacent to a nitrogen atom in amides and sulfonamides with the N-H bond in azoles proceeded smoothly in the presence of
Sofia Tresintsi et al.
Water research, 46(16), 5255-5267 (2012-07-25)
Various iron oxy-hydroxides were synthesized in a continuous flow kilogram-scale production reactor through the precipitation of FeSO(4) and FeCl(2) in the pH range 3-12 under intense oxidative conditions to serve as arsenic adsorbents. The selection of the optimum adsorbent and
Chong Qin et al.
Angewandte Chemie (International ed. in English), 51(28), 6971-6975 (2012-06-13)
Ironing it out: an efficient and convenient nitrogenation strategy involving C-C bond cleavage for the straightforward synthesis of versatile arylamines is presented. Various alkyl azides and alkylarenes, including the common industrial by-product cumene, react using this protocol. Moreover, this method

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