Ferric EDTA is the coordination complex formed from ferric ions and EDTA. EDTA has a high affinity for ferric ions. It is a yellow solid that gives yellowish aqueous solutions. Solutions of Fe(III)-EDTA are produced by combining ferrous salts and aqueous solutions of EDTA known as Jacobson's solution (cf. chemical equation (1) under Table (1)). Near neutral pH, the principal complex is [Fe(EDTA)(H2O)]−, although most sources ignore the aquo ligand. The [Fe(EDTA)(H2O)]− anion has been crystallized with many cations, e.g., the trihydrate Na[Fe(EDTA)(H2O)].2H2O. The salts as well as the solutions are yellow-brown. Provided the nutrient solution in which the [Fe(EDTA)(H2O)]− complex will be used has a pH of at least 5.5, all the uncomplexed iron, as a result of incomplete synthesis reaction, will still change into the chelated ferric form. In contact with aerated natural waters, iron salts convert to the ferric form. Near neutral pH, ferric ions form insoluble solids and are thus not bioavailable. EDTA (and other chelating agents) address this problem, by forming soluble complexes that resist formation of hydroxides. Together with pentetic acid (DTPA), EDTA is widely used for sequestering metal ions. Otherwise these metal ions catalyze the decomposition of hydrogen peroxide, which is used to bleach pulp in papermaking. Several million kilograms EDTA are produced for this purpose annually. Iron chelate is commonly used for agricultural purposes to treat chlorosis, a condition in which leaves produce insufficient chlorophyll. Iron and ligand are absorbed separately by the plant roots whereby the highly stable ferric chelate is first reduced to the less stable ferrous chelate. In horticulture, iron chelate is often referred to as 'sequestered iron' and is used as a plant tonic, often mixed with other nutrients and plant foods (e.g. seaweed). It is recommended in ornamental horticulture for feeding ericaceous plants like Rhododendrons if they are growing in calcareous soils.