Iron II sulfate

Sellaite, see Magnesium fluoride Senarmontite, see Antimony(III) oxide Siderite, see Iron(II) carbonate Siderotil, see Iron(II) sulfate 5-water Silica, see Silicon dioxide Silicotungstic acid, see Silicon oxide—tungsten oxide—water (1/12/26)... 

Tris( 1,10-phenanthroline)-iron(II) sulfate 1.06 (I.OOMH2SO4) Red to faint blue... 

Manganese(II) can be titrated directly to Mn(III) using hexacyanoferrate(III) as the oxidant. Alternatively, Mn(III), prepared by oxidation of the Mn(II)-EDTA complex with lead dioxide, can be determined by titration with standard iron(II) sulfate. 

Methylpyridine Hydrogen peroxide, iron(II) sulfate, sulfuric acid... 

Tetrasodium hexakiscyanoferrate decahydrate [14434-22-1], Na4[Fe(CN)g] IOH2O, or yellow pmssiate of soda, forms yellow monoclinic crystals that are soluble in water but insoluble in alcohol. It is slightly efflorescent at room temperature, but the anhydrous material, tetrasodium hexakiscyanoferrate [13601 -19-9], Na4[Fe(CN)J, is obtained at 100°C. The decahydrate is produced from calcium cyanide, iron(II) sulfate, and sodium carbonate in a process similar to that for the production of K4[Fe(CN)g] 3H2O. It is used in the manufacture of trisodium hexakiscyanoferrate, black and blue dyes, as a metal surface coating, and in photographic processing. 

Nitrates. Iron(II) nitrate hexahydrate [14013-86-6], Fe(N03)2 6H20, is a green crystalline material prepared by dissolving iron in cold nitric acid that has a specific gravity of less than 1.034 g/cm. Use of denser, more concentrated acid leads to oxidation to iron(III). An alternative method of preparation is the reaction of iron(II) sulfate and barium or lead nitrate. The compound is very soluble in water. Crystallisation at temperatures below — 12°C affords an nonahydrate. Iron(II) nitrate is a useful reagent for the synthesis of other iron-containing compounds and is used as a catalyst for reduction reactions. 

Sulfates. Iron(II) sulfate heptahydrate [7782-63-0] FeSO forms blue-green monoclinic crystals that are very soluble in water and... 

C. Further warming to 65°C forms white iron sulfate monohydrate [17375-41 -6], FeSO H2O, which is stable to 300°C. Strong beating results in decomposition with loss of sulfur dioxide. Solutions of iron(II) sulfate reduce nitrate and nitrite to nitric oxide, whereupon the highly colored [Fe(H20) (N0)] ion is formed. This reaction is the basis of the brown ring text for the quaUtative deterrnination of nitrate or nitrite. 

Iron(II) sulfate forms double salts of formula M2SO4 FeSO 6H20 with aLkaU sulfates. Iron(II) ammonium sulfate [7783-85-9] (Mohr s salt),... 

FeSO (NH 2S04 6H20, is used as a primary standard for iron. It is soluble in water but insoluble in alcohols. Both the soHd and its solution are more stable to oxidation than iron(II) sulfate. 

The main impurity of the filtrate is the iron(II) sulfate which can be crystallized as the heptahydrate, FeS04-7H2 O, by cooling the solution to a temperature below 15°C. This process is most often carried out in vacuum crystallizers. The crystals of iron sulfate are separated by centrifugation or filtration (qv). To prevent premature hydrolysis of titanium dioxide, the temperature of the above processes should not exceed 70°C. 

The largest volume of synthetic red iron oxide is produced by the two-step calcination of iron(II) sulfate. In the first step, the iron(II) sulfate heptahydrate is dehydrated to a monohydrate ... 

In the direct precipitation process, the seeds of iron(III) oxide are added to an iron salt solution, most often iron(II) sulfate, which is subsequendy oxidized by air. The released sulfuric acid is removed by the addition of metallic iron with which it reacts to iron(II) sulfate. The overall reaction shows that ferrous sulfate is not consumed during the process. It only helps to oxidize metallic iron to ferric oxide ... 

More specifically, 2-aminophenol can be detected in solution using an iron(II) sulfate—hydrogen peroxide reagent (94). 3- Aminopheno1 has been analyzed colorimetrically by oxidation in base and subsequent extraction of a violet quinoneimide dye (95). A colorimetric method using... 

The use of free-radical reactions for this mode of ring formation has received rather more attention. The preparation of benzo[Z)]thiophenes by pyrolysis of styryl sulfoxides or styryl sulfides undoubtedly proceeds via formation of styrylthiyl radicals and their subsequent intramolecular substitution (Scheme 18a) (75CC704). An analogous example involving an amino radical is provided by the conversion of iV-chloro-iV-methylphenylethylamine to iV-methylindoline on treatment with iron(II) sulfate in concentrated sulfuric acid (Scheme 18b)(66TL2531). 

Dipping solution Dissolve 3 g 1-naphthol in 150 ml methanol and add 1350 ml water. Dissolve 0.5 g potassium disulfite (potassium metabisulfite) in this solution, add 20 ml glacial acetic acid and dissolve 0.5 g iron(II) sulfate THiO followed by 2.2 g N -ethyl-N -(2-methanesulfonamidoethyl)-2-methyl-l,4-phenylenediamine (sesquisulfate, monohydrate) (color developer 3, Merck). Care should be taken at each step that the solution has clarified before adding further components. 

Color developer 3 Potassium disulfite Iron(II) sulfate heptahydrate Methanol... 

The anodic oxidation of the iron is usually localized in surface pits and crevices which allow the formation of adherent rust over the remaining surface area. Eventually the lateral extension of the anodic area undermines the rust to produce loose flakes. Moreover, once an adherent film of rust has formed, simply painting over gives but poor protection. This is due to the presence of electrolytes such as iron(II) sulfate in the film so that painting merely seals in the ingredients for anodic oxidation. It then only requites the exposure of some other portion of the surface, where cathodic reduction can take place, for rusting beneath the paint to occur. 

Ammonium-ferrisulfat, n. ammonium iron(III). sulfate, ferric ammonium sulfate, -ferro-sulfat, n. ammonium iron(II) sulfate, ferrous ammonium sulfate, -jodat, n. ammonium iodate. -jodid, n. ammonium iodide, -platinchlorid, n. ammonium platinichloride (chloroplatinate). -rest, m. ammonium radical. rhodanid, -rhodantir, n. ammonium thiocyanate, -salpeter, m. ammonium nitrate, -salz, n. ammonium s t. -selfe,/. ammonia soap, -sulfhydrat, n. ammonium hydrosulfide, -sulfocyanid, n. ammonium thiocyanate, -verbindung,/. ammonium compound, -zinn-chlorid, n. ammonium chlorostannate, pink salt. 

Eisenoxydul-hydrat, n. ferrous hydroxide, iron(ll) hydroxide, -oxyd, n. ferrosoferric oxide, iron(II,III) oxide, magnetic iron oxide (FeaOi). -salz, n. ferrous salt, iron(II) salt, -sulfat, n. ferrous sulfate, iron(II) sulfate, -verbindung, /. ferrous compound, iron(ll) compound. 

When 25.0 mL of0.500 M iron(II) sulfate is combined with 35.0 mL of 0.332 M barium hydroxide, two different precipitates are formed. 

When hemin (1) is treated with gaseous hydrogen chloride in anhydrous methanol/pyridine in the presence of iron(II) sulfate, protoporphyrin dimethyl ester (2), the metal-free ligand of hemin. is produced in almost quantitative yield. This compound is quite sensitive to oxygen... 

This ring system could be prepared by building either of the two heterocycles and then doing an annulation. Thus, cyclization of ethyl o-nitrophenylhydrazonocyanoacetyl carbamate 552 afforded 553. Reduction of 553 by the action of iron(II) sulfate gave 554, which on acid hydrolysis gave 558. Cyclization of o-aminophenyl derivatives 554 and 558 to 555 and 559, respectively, was effected (77CCC894) by treatment with acid. Phthalimido derivatives of 554 could also be cyclized to this... 

Peroxides Iron(II) sulfate + ammonium thiocyanate Peroxides rapidly oxidize iron(II) to iron(III) ions which react to yield brown-red iron(III) thiocyanate complexes. [31, 32]... 

A galvanic cell can be constmcted from a zinc electrode immersed in a solution of zinc sulfate and an iron electrode immersed in a solution of iron(II) sulfate. What is the standard potential of this cell, and what is its spontaneous direction under standard conditions ... 

The S-methyldithiocarbazates of both 2-formylquinoline, 18, and 1-formyliso-quinoline, 19, yield diamagnetic green [FeL2] complexes from iron(II) sulfate [131]. Coordination for both complexes is via the ring nitrogen, azomethine nitrogen and thiol sulfur based on infrared studies. 

---