Hexahydrate sorbitol formula

iron(II) sulfate, when dissolved in water

IUPAC name

Iron(II) sulfate

Other names

Ferrous sulfate, Green vitriol, Iron vitriol, Copperas, Melanterite, Szomolnokite

ECHA InfoCard 100.028.867
EC Number 231-753-5
RTECS number NO8500000 (anhydrous)
NO8510000 (heptahydrate)
UN number 3077
Molar mass 151.91 g/mol (anhydrous)
169.93 g/mol (monohydrate)
241.99 g/mol (pentahydrate)
260.00 g/mol (hexahydrate)
278.02 g/mol (heptahydrate)
Appearance White crystals (anhydrous)
White-yellow crystals (monohydrate)
Blue-green crystals (heptahydrate)
Odor Odorless
Density 3.65 g/cm3 (anhydrous)
3 g/cm3 (monohydrate)
2.15 g/cm3 (pentahydrate)
1.934 g/cm3 (hexahydrate)
1.895 g/cm3 (heptahydrate)
Melting point 680 °C (1,256 °F; 953 K)
(anhydrous) decomposes
300 °C (572 °F; 573 K)
(monohydrate) decomposes
60–64 °C (140–147 °F; 333–337 K)
(heptahydrate) decomposes
44.69 g/100 mL (77 °C)
35.97 g/100 mL (90.1 °C)
15.65 g/100 mL (0 °C)
20.5 g/100 mL (10 °C)
29.51 g/100 mL (25 °C)
39.89 g/100 mL (40.1 °C)
51.35 g/100 mL (54 °C)
Solubility Negligible in alcohol
Solubility in ethylene glycol 6.4 g/100 g (20 °C)
Vapor pressure 1.95 kPa (heptahydrate)
6998124000000000000♠1.24×10−2 cm3/mol (anhydrous)
6998105000000000000♠1.05×10−2 cm3/mol (monohydrate)
6998112000000000000♠1.12×10−2 cm3/mol (heptahydrate)
6998101999999999999♠+10200×10−6 cm3/mol
1.591 (monohydrate)
1.526–1.528 (21 °C, tetrahydrate)
1.513–1.515 (pentahydrate)
1.468 (hexahydrate)
1.471 (heptahydrate)
Orthorhombic, oP24 (anhydrous)
Monoclinic, mS36 (monohydrate)
Monoclinic, mP72 (tetrahydrate)
Triclinic, aP42 (pentahydrate)
Monoclinic, mS192 (hexahydrate)
Monoclinic, mP108 (heptahydrate)
Pnma, No. 62 (anhydrous)
C2/c, No. 15 (monohydrate, hexahydrate)
P21/n, No. 14 (tetrahydrate)
P1, No. 2 (pentahydrate)
P21/c, No. 14 (heptahydrate)
2/m 2/m 2/m (anhydrous)
2/m (monohydrate, tetrahydrate, hexahydrate, heptahydrate)
1 (pentahydrate)

a  = 8.704(2) Å,

b  = 6.801(3) Å,

c  = 4.786(8) Å (293 K, anhydrous)

α = 90°, β = 90°, γ = 90°

Octahedral (Fe2+)
100.6 J/mol·K (anhydrous)
394.5 J/mol·K (heptahydrate)
107.5 J/mol·K (anhydrous)
409.1 J/mol·K (heptahydrate)
−928.4 kJ/mol (anhydrous)
−3016 kJ/mol (heptahydrate)
−820.8 kJ/mol (anhydrous)
−2512 kJ/mol (heptahydrate)
B03AA07 (WHO)
GHS pictograms
GHS signal word Warning
H302, H315, H319
NFPA 704
Lethal dose or concentration (LD, LC):
237 mg/kg (rat, oral)
US health exposure limits (NIOSH):
TWA 1 mg/m3
Cobalt(II) sulfate

Copper(II) sulfateManganese(II) sulfateNickel(II) sulfate

Related compounds

Iron(III) sulfate

Except where otherwise noted, data are given for materials in their

standard state

(at 25 °C , 100 kPa).

N verify (what is YN ?)
Infobox references

Iron(II) sulfate (British English: iron(II) sulphate) or ferrous sulfate denotes a range of salts with the formula FeSO4·xH2O. These compounds exist most commonly as the heptahydrate (x = 7) but are known for several values of x. The hydrated form is used medically to treat iron deficiency, and also for industrial applications. Known since ancient times as copperas and as green vitriol, the blue-green heptahydrate is the most common form of this material. All the iron(II) sulfates dissolve in water to give the same aquo complex 2+, which has octahedral molecular geometry and is paramagnetic. The name copperas dates from times when the copper(II) sulfate was known as blue copperas, and perhaps in analogy, iron(II) and zinc sulfate were known respectively as green and white copperas.

It is on the World Health Organization’s List of Essential Medicines, the most important medications needed in a basic health system.


Industrially, ferrous sulfate is mainly used as a precursor to other iron compounds. It is a reducing agent, and as such is useful for the reduction of chromate in cement to less toxic Cr(III) compounds. Historically ferrous sulfate was used in the textile industry for centuries as a dye fixative. It is used historically to blacken leather and as a constituent of ink.

Medical use

Together with other iron compounds, ferrous sulfate is used to fortify foods and to treat and prevent iron deficiency anemia. Constipation is a frequent and uncomfortable side effect associated with the administration of oral iron supplements. Stool softeners often are prescribed to prevent constipation.


Ferrous sulfate was used in the manufacture of inks, most notably iron gall ink, which was used from the middle ages until the end of the eighteenth century. Chemical tests made on the Lachish letters (c.588–586 BCE) showed the possible presence of iron. It is thought that oak galls and copperas may have been used in making the ink on those letters. It also finds use in wool dyeing as a mordant. Harewood, a material used in marquetry and parquetry since the 17th century, is also made using ferrous sulfate.

Two different methods for the direct application of indigo dye were developed in England in the eighteenth century and remained in use well into the nineteenth century. One of these, known as china blue, involved iron(II) sulfate. After printing an insoluble form of indigo onto the fabric, the indigo was reduced to leuco-indigo in a sequence of baths of ferrous sulfate (with reoxidation to indigo in air between immersions). The china blue process could make sharp designs, but it could not produce the dark hues of other methods. Sometimes, it is included in canned black olives as an artificial colorant.

Ferrous sulfate can also be used to stain concrete and some limestones and sandstones a yellowish rust color.

Woodworkers use ferrous sulfate solutions to color maple wood a silvery hue.

Other uses

In horticulture it is used for treating iron chlorosis. Although not as rapid-acting as iron chelate, its effects are longer-lasting. It can be mixed with compost and dug into to the soil to create a store which can last for years. It is also used as a lawn conditioner, and moss killer.

In the second half of the 1850s ferrous sulfate was used as a photographic developer for collodion process images.

Ferrous sulfate is sometimes added to the cooling water flowing through the brass tubes of turbine condensers to form a corrosion-resistant protective coating.

It is used in gold refining to precipitate metallic gold from auric chloride solutions (gold dissolved in solution with aqua regia).

It has been used in the purification of water by flocculation and for phosphate removal in municipal and industrial sewage treatment plants to prevent eutrophication of surface water bodies.

It is used as a traditional method of treating wood panelling on houses, either alone, dissolved in water, or as a component of water-based paint.

Green vitriol is also a useful reagent in the identification of mushrooms.


Iron(II) sulfate can be found in various states of hydration, and several of these forms exist in nature.

  • FeSO4·H2O (mineral: Szomolnokite, relatively rare)
  • FeSO4·4H2O (mineral: Rozenite, white, relatively common, may be dehydratation product of melanterite)
  • FeSO4·5H2O (mineral: Siderotil, relatively rare)
  • FeSO4·6H2O (mineral: Ferrohexahydrite, relatively rare)
  • FeSO4·7H2O (mineral: Melanterite, blue-green, relatively common)

Anhydrous iron(II) sulfate

The tetrahydrate is stabilized when the temperature of aqueous solutions reaches 56.6 °C (133.9 °F). At 64.8 °C (148.6 °F) these solutions form both the tetrahydrate and monohydrate.

All mentioned mineral forms are connected with oxidation zones of iron-bearing ore beds (pyrite, marcasite, chalcopyrite, etc.) and related environments (like coal fire sites). Many undergo rapid dehydration and sometimes oxidation.

Production and reactions

In the finishing of steel prior to plating or coating, the steel sheet or rod is passed through pickling baths of sulfuric acid. This treatment produces large quantities of iron(II) sulfate as a by-product.

Fe + H2SO4 → FeSO4 + H2

Another source of large amounts results from the production of titanium dioxide from ilmenite via the sulfate process.

Ferrous sulfate is also prepared commercially by oxidation of pyrite:

2 FeS2 + 7 O2 + 2 H2O → 2 FeSO4 + 2 H2SO4


Upon dissolving in water, ferrous sulfates form the metal aquo complex 2+, which is an almost colorless, paramagnetic ion.

On heating, iron(II) sulfate first loses its water of crystallization and the original green crystals are converted into a brown colored anhydrous solid. When further heated, the anhydrous material releases sulfur dioxide and white fumes of sulfur trioxide, leaving a reddish-brown iron(III) oxide. Decomposition of iron(II) sulfate begins at about 680 °C (1,256 °F).

2 FeSO4 → Fe2O3 + SO2 + SO3

Like all iron(II) salts, iron(II) sulfate is a reducing agent. For example, it reduces nitric acid to nitrogen monoxide and chlorine to chloride:

6 FeSO4 + 3 H2SO4 + 2 HNO3 → 3 Fe2(SO4)3 + 4 H2O + 2 NO 6 FeSO4 + 3 Cl2 → 2 Fe2(SO4)3 + 2 FeCl3

Upon exposure to air, it oxidizes to form a corrosive brown-yellow coating of “basic ferric sulfate”, which is an adduct of iron(III) oxide and iron(III) sulfate:

12 FeSO4 + 3 O2 → 4 Fe2(SO4)3 + 2 Fe2O3

See also

  • Iron(III) sulfate (ferric sulfate), the other common simple sulfate of iron.
  • Copper(II) sulfate
  • Ammonium iron(II) sulfate, also known as Mohr’s salt, the common double salt of ammonium sulfate with iron(II) sulfate.
  • Chalcanthum
  • Ephraim Seehl known as an early manufacturer of green vitriol.


  1. ^ a b c d e f “Siderotil Mineral Data”. Retrieved 2014-08-03. 
  2. ^ a b c d e f “Ferrohexahydrite Mineral Data”. Retrieved 2014-08-03. 
  3. ^ a b c d e f g h Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0. 
  4. ^ a b Seidell, Atherton; Linke, William F. (1919). Solubilities of Inorganic and Organic Compounds (2nd ed.). New York: D. Van Nostrand Company. p. 343. 
  5. ^ a b Anatolievich, Kiper Ruslan. “iron(II) sulfate”. Retrieved 2014-08-03. 
  6. ^ a b c d Sigma-Aldrich Co., Iron(II) sulfate heptahydrate. Retrieved on 2014-08-03.
  7. ^ a b c d e Ralph, Jolyon; Chautitle, Ida. “Szomolnokite”. Mindat.org. Retrieved 2014-08-03. 
  8. ^ a b c d e “Rozenite Mineral Data”. Retrieved 2014-08-03. 
  9. ^ a b c d e “Melanterite Mineral Data”. Retrieved 2014-08-03. 
  10. ^ a b c “MSDS of Ferrous sulfate heptahydrate”. Fair Lawn, New Jersey: Fisher Scientific, Inc. Retrieved 2014-08-03. 
  11. ^ a b c d Weil, Matthias (2007). “The High-temperature β Modification of Iron(II) Sulfate”. Acta Crystallographica Section E. International Union of Crystallography. (12): i192. doi:10.1107/S160053680705475X. Retrieved 2014-08-03. 
  12. ^ a b c d Anatolievich, Kiper Ruslan. “iron(II) sulfate heptahydrate”. Retrieved 2014-08-03. 
  13. ^ “NIOSH Pocket Guide to Chemical Hazards #0346”. National Institute for Occupational Safety and Health (NIOSH). 
  14. ^ Brown, Lesley (1993). The New shorter Oxford English dictionary on historical principles. Oxford : Clarendon. ISBN 0-19-861271-0. 
  15. ^ “WHO Model List of Essential Medicines (19th List)” (PDF). World Health Organization. April 2015. Retrieved 8 December 2016. 
  16. ^ British Archeology magazine.
  17. ^ Torczyner, Lachish Letters, pp. 188–95
  18. ^ Hyatt, The Interpreter’s Bible, 1951, volume V, p. 1067
  19. ^ How To Stain Concrete with Iron Sulfate
  20. ^ Koenig, Rich and Kuhns, Mike: Control of Iron Chlorosis in Ornamental and Crop Plants. (Utah State University, Salt Lake City, August 1996) p.3
  21. ^ a b Handreck, Kevin (2002). Gardening Down Under: A Guide to Healthier Soils and Plants (2nd ed.). Collingwood, Victoria: CSIRO Publishing. pp. 146–47. ISBN 0-643-06677-2. 
  22. ^ Svrček, Mirko (1975). A color guide to familiar mushrooms (2nd ed.). London: Octopus Books. p. 30. ISBN 0-7064-0448-3. 
  23. ^ Wildermuth, Egon; Stark, Hans; Friedrich, Gabriele; Ebenhöch, Franz Ludwig; Kühborth, Brigitte; Silver, Jack; Rituper, Rafael (2005), “Iron Compounds”, Ullmann’s Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH 
  24. ^ Pryce, William (1778). Mineralogia Cornubiensis; a Treatise on Minerals, Mines and Mining. London: Phillips. p. 33. 

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