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157740

Iron(III) chloride

greener alternative

reagent grade, 97%

Synonym(s):

Ferric chloride, Iron trichloride, Molysite

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About This Item

Linear Formula:
FeCl3
CAS Number:
Molecular Weight:
162.20
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-729-4
MDL number:
Assay:
97%
Grade:
reagent grade
Form:
powder
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grade

reagent grade

Quality Level

vapor density

5.61 (vs air)

vapor pressure

1 mmHg ( 194 °C)

assay

97%

form

powder

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

304 °C (lit.)

greener alternative category

SMILES string

Cl[Fe](Cl)Cl

InChI

1S/3ClH.Fe/h3*1H;/q;;;+3/p-3

InChI key

RBTARNINKXHZNM-UHFFFAOYSA-K

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Iron(III) chloride is a mild oxidizing agent and participates in various carbon-carbon-bond forming reactions. On crystallization with water, it forms hydrates. It can be prepared by reacting chlorine with the scrap iron at approximately 650°C.

Application

The vapor-phase co-reductions with other metal halides by hydrogen results in finely divided intermetallics with applications as structural materials or compounds with useful thermoelectric, magnetic, and oxidation-resitance properties.
Iron(III) chloride (Ferric Chloride, FeCl3) has been used as a surface modulator for the characterization of wines by fingerprinting technology. It has been used for the quantitative estimation of sulfide in various biological samples.


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CorrosionExclamation mark

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Storage Class

13 - Non Combustible Solids



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"Iron (III) chloride-catalyzed convenient one-pot synthesis of homoallyl benzyl ethers starting from aldehydes"
Watahiki T, et al.
Organic Letters, 5(17), 3045-3048 (2003)
Novel non-specific liquid fingerprint technology for wine analysis: a feasibility study.
Siivonen JJ, et al.
Australian Journal of Grape and Wine Research, 20(2), 172-177 (2014)
"Iron (III) chloride-based mild synthesis of phenanthrene and its application to total synthesis of phenanthroindolizidine alkaloids"
Wang L-K, et al.
Tetrahedron, 64(32), 7504-7510 (2008)



Global Trade Item Number

SKUGTIN
157740-100G04061835276493
157740-2.5KG04061835276516
157740-1KG04061835276509
157740-5G04061835276523