All Photos(3)

372870

Sigma-Aldrich

Iron(II) chloride

greener alternative

98%

Synonym(s):
Iron dichloride, Ferrous chloride
Linear Formula:
FeCl2
CAS Number:
Molecular Weight:
126.75
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

powder

reaction suitability

core: iron
reagent type: catalyst
reaction type: Atom Transfer Radical Polymerization (ATRP)

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

mp

677 °C (lit.)

density

3.16 g/mL at 25 °C (lit.)

greener alternative category

Aligned

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

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. The iron catalysts are known to be inexpensive and environmentally benign. Click here for more information.

Application

Iron(II) chloride can be used to catalyze:
  • The preparation of Grignard compounds, such as 1-naphthylmagnesium chloride.
  • The selective oxidation of 2,4,6-trimethylphenol (2,4,6-TMP) to 3,5-dimethyl-4-hydroxybenzaldehyde (DMHB) in the presence of acetoxime.
  • Raney-type catalysts modified with FeCl2 show enhanced selective hydrogenation of an α,β-unsaturated aldehyde to an unsaturated alcohol.

Packaging

25, 250 g in glass bottle

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

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

Certificate of Analysis

Certificate of Origin

Transition metal catalyzed preparation of Grignard compounds.
Bogdanovic B, et al.
Angewandte Chemie (International Edition in English), 39(24), 4610-4612 (2000)
2, 4, 6-Trimethylphenol oxidation with ferrous chloride catalyst: Effect of acetoxime addition.
Li K, et al.
J. Mol. Catal. A: Chem., 241(1-2), 72-78 (2005)
Liquid-phase Selective Hydrogenation of an Aliphatic ?, ?-Unsaturated Aldehyde over Raney Cobalt Catalyst Modified with Ferrous Chloride.
Hotta K, et al.
Bulletin of the Chemical Society of Japan, 42(5), 1447-1449 (1969)
Gustavo A Molina et al.
Polymers, 12(4) (2020-04-15)
In this study, new polyurethanes (PUs) were prepared by using inulin and polycaprolactone as polyols. Their structure and morphology were determined by Fourier transform infrared spectroscopy (FTIR), Raman dispersive spectroscopy, Nuclear magnetic resonance spectroscopy (1H NMR and 13C NMR), and...
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...

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