Iron(II) hydroxide is poorly soluble (1.43 × 10−3 g/L). It precipitates from from the reaction of iron(II) sulfate and hydroxide ions (from a soluble compound containing hydroxide ion):
It is also easily formed as an undesirable by-product of other reactions, a.o., in the synthesis of siderite, an iron carbonate (FeCO3), if the crystal growth conditions are poorly controlled (reagent concentrations, addition rate, addition order, pH, pCO2, T, ageing time, ...).
Anions such as selenite and selenate can be easily adsorbed on the positively charged surface of green rust where they are subsequently reduced by Fe2+. The resulting products being poorly soluble (Se0, FeSe, or FeSe2).
Ferrous hydroxide has also been investigated as an agent for the removal of toxic selenate and selenite ions from water systems such as wetlands. The ferrous hydroxide reduces these ions to elemental selenium, which is insoluble in water and precipitates out.
Note: pKsp = 15.097 where p is the -log and Ksp is the Solubility Product Constant. This means it has a low tendency to dissolve, but is not entirely insoluble. An acidic solution would allow this to disassociate more because the H+ would react with the OH- in the compound.
In a basic solution (potassium hydroxide), ferrous hydroxide is the electrochemically active material of the negative electrode of the Nickel-iron battery.