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450944

Sigma-Aldrich

Iron(II) chloride

AnhydroBeads™, −10 mesh, 99.9% trace metals basis

Sinónimos:

Ferrous chloride, Iron dichloride

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About This Item

Fórmula lineal:
FeCl2
Número de CAS:
7758-94-3
Peso molecular:
126.75
EC Number:
231-843-4
MDL number:
MFCD00011004
UNSPSC Code:
12352302
PubChem Substance ID:
24868593
NACRES:
NA.23

product line

AnhydroBeads™

Quality Level

100

assay

99.9% trace metals basis

reaction suitability

reagent type: catalyst
core: iron

impurities

≤1500.0 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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Application

Used in the synthesis of a novel cis-Fe(BPE5)2Cl2 (BPE5=1,2-diphospholanoethane) complex, which has potential application in many types of reactions such as intra- or intermolecular activation.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

For use with

Referencia del producto
Descripción
Precios

Pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

does not flash

flash_point_c

does not flash

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Field, L.D. et al.
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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