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Key Documents

157740

Sigma-Aldrich

Iron(III) chloride

greener alternative

reagent grade, 97%

Synonyma:

Ferric chloride, Iron trichloride, Molysite

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About This Item

Lineární vzorec:
FeCl3
Číslo CAS:
Molekulová hmotnost:
162.20
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

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
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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

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General description

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.
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Application

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.
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.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Novel non-specific liquid fingerprint technology for wine analysis: a feasibility study.
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Australian Journal of Grape and Wine Research, 20(2), 172-177 (2014)
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Wang L-K, et al.
Tetrahedron, 64(32), 7504-7510 (2008)
"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)
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