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Sigma-Aldrich

Iron(II) chloride

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

Synonym(s):

Ferrous chloride, Iron dichloride

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About This Item

Linear Formula:
FeCl2
CAS Number:
7758-94-3
Molecular Weight:
126.75
EC Number:
231-843-4
MDL number:
MFCD00011004
UNSPSC Code:
12352302
PubChem Substance ID:
24868593
NACRES:
NA.23

product line

AnhydroBeads™

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

accessory

Product No.
Description
Pricing

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘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
Laurean Ilies et al.
Journal of the American Chemical Society, 134(41), 16951-16954 (2012-10-05)
Diarylalkynes are chemo- and stereoselectively hydromagnesiated in high yields at room temperature with an iron species generated in situ from FeCl(2)and EtMgBr. Functional groups such as bromide, iodide, amine, phenoxide, and alkene are well tolerated. Under similar conditions, diynes are
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