structure of anhydrous ferrous chloride (purple = Fe, green = Cl)
structure of tetrahydrate
|3D model (Jmol)||Interactive image|
|Molar mass||126.751 g/mol (anhydrous)
198.8102 g/mol (tetrahydrate)
|Appearance||tan solid (anhydrous)
pale green solid (di-tetrahydrate)
|Density||3.16 g/cm3 (anhydrous)
2.39 g/cm3 (dihydrate)
1.93 g/cm3 (tetrahydrate)
|Melting point||677 °C (1,251 °F; 950 K) (anhydrous)
120 °C (dihydrate)
105 °C (tetrahydrate) 
|Boiling point||1,023 °C (1,873 °F; 1,296 K) (anhydrous)|
|64.4 g/100 mL (10 °C),
68.5 g/100mL (20 °C),
105.7 g/100 mL (100 °C)
|Solubility in THF||soluble|
|Solubility in ethanol||100 g/100 mL (value should be double checked , experiment shows merely soluble(anhydrous))|
|octahedral at Fe|
|US health exposure limits (NIOSH):|
|TWA 1 mg/m3|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Iron(II) chloride, also known as ferrous chloride, is the chemical compound of formula FeCl2. It is a paramagnetic solid with a high melting point. The compound is white, but typical samples are often off-white. FeCl2 crystallizes from water as the greenish tetrahydrate, which is the form that is most commonly encountered in commerce and the laboratory. There is also a dihydrate. The compound is also soluble in water; aqueous solutions of FeCl2 are highly transparent and pale green in color.
Hydrated forms of ferrous chloride are generated by treatment of wastes from steel production with hydrochloric acid. Such solutions are designated "spent acid," especially when the hydrochloric acid is not completely consumed:
The dihydrate crystallizes from concentrated hydrochloric acid.
Ferrous chloride is conveniently prepared by addition of iron powder to a solution of methanol and concentrated hydrochloric acid under an inert atmosphere. This reaction gives the methanol solvate, which upon heating in a vacuum at about 160 °C gives anhydrous FeCl2. FeBr2 and FeI2 can be prepared analogously.
- Fe + 2 HCl → FeCl2 + H2
- 2 FeCl3 + C6H5Cl → 2 FeCl2 + C6H4Cl2 + HCl
FeCl2 is soluble in tetrahydrofuran (THF). In one of two classic syntheses of ferrocene, Wilkinson generated FeCl2 by heating FeCl3 with iron powder in THF. Ferric chloride decomposes to ferrous chloride at high temperatures.
FeCl2 and its hydrates form complexes with many ligands. The anhydrous FeCl2 is a standard precursor in organometallic synthesis. Solutions of the hydrates react with two molar equivalents of [(C2H5)4N]Cl to give the salt [(C2H5)4N]2[FeCl4].
Ferrous chloride has a variety of niche applications, but the related compounds ferrous sulfate and ferric chloride enjoy more applications. Aside from use in the laboratory synthesis of iron complexes, ferrous chloride serves as a reducing flocculating agent in wastewater treatment, especially for wastes containing chromate. It is the precursor to hydrated iron(III) oxides that are magnetic pigments. Ferrous chloride is employed as a reducing agent in many organic synthesis reactions.
- Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
- "NIOSH Pocket Guide to Chemical Hazards #0346". National Institute for Occupational Safety and Health (NIOSH).
- Egon Wildermuth, Hans Stark, Gabriele Friedrich, Franz Ludwig Ebenhöch, Brigitte Kühborth, Jack Silver, Rafael Rituper “Iron Compounds” in Ullmann’s Encyclopedia of Industrial Chemistry Wiley-VCH, Wienheim, 2005.
- K. H.. Gayer; L. Woontner (1957). "Iron(II) Chloride 2-Hydrate". Inorg. Synth. 5: 179–181. doi:10.1002/9780470132364.ch48.
- G. Winter; Thompson, D. W.; Loehe, J. R. (1973). "Iron(II) Halides". Inorg. Synth. 14: 99–104. doi:10.1002/9780470132456.ch20.
- P. Kovacic and N. O. Brace (1960). "Iron(II) Chloride". Inorg. Synth. 6: 172. doi:10.1002/9780470132371.ch54.
- G. Wilkinson (1963). "Ferrocene". Org. Synth.; Coll. Vol., 4, p. 473
- Morosin, B.; Graeber, E. J. (1965). "Crystal structures of manganese(II) and iron(II) chloride dihydrate". Journal of Chemical Physics. 42: 898–901. doi:10.1063/1.1696078.
- N. S. Gill, F. B. Taylor (1967). "Tetrahalo Complexes of Dipositive Metals in the First Transition Series". Inorg. Synth. 9: 136–142. doi:10.1002/9780470132401.ch37.