Stannic, stannous chlorides

Both aliphatic and aromatic nitro-compounds can be readily reduced in acid solution to the corresponding primary amine. Thus when a mixture of nitrobenzene and tin is treated with hydrochloric acid, the tin dissolves to give stannous chloride, SnCh, which in these circumstances then reacts with more acid to give stannic chloride, SnCl, and the nascent hydrogen produced from... 

Stannic and stannous chloride are best prepared by the reaction of chlorine with tin metal. Stannous salts are generally prepared by double decomposition reactions of stannous chloride, stannous oxide, or stannous hydroxide with the appropriate reagents. MetaUic stannates are prepared either by direct double decomposition or by fusion of stannic oxide with the desired metal hydroxide or carbonate. Approximately 80% of inorganic tin chemicals consumption is accounted for by tin chlorides and tin oxides. 

Halides. The tin haUdes of the greatest commercial importance are stannous chloride, stannic chloride, and stannous fluoride. Tin hahdes of less commercial importance are stannic bromide [7789-67-5], stannic iodide [7790-47-8], stannous bromide [10031-24-0], and stannous iodide [10294-70-9] ( ) ... 

Anhydrous stannous chloride, a water-soluble white soHd, is the most economical source of stannous tin and is especially important in redox and plating reactions. Preparation of the anhydrous salt may be by direct reaction of chlorine and molten tin, heating tin in hydrogen chloride gas, or reducing stannic chloride solution with tin metal, followed by dehydration. It is soluble in a number of organic solvents (g/100 g solvent at 23°C) acetone 42.7, ethyl alcohol 54.4, methyl isobutyl carbinol 10.45, isopropyl alcohol 9.61, methyl ethyl ketone 9.43 isoamyl acetate 3.76, diethyl ether 0.49, and mineral spirits 0.03 it is insoluble in petroleum naphtha and xylene (2). 

Stannous Chloride Dihydrate. A white crystalline soHd, stannous chloride dihydrate is prepared either by treatment of granulated tin with hydrochloric acid followed by evaporation and crystallisation or by reduction of a stannic chloride solution with a cathode or tin metal followed by crystallisation. It is soluble in methanol, ethyl acetate, glacial acetic acid, sodium hydroxide solution, and dilute or concentrated hydrochloric acid. It is soluble in less than its own weight of water, but with much water it forms an insoluble basic salt. 

Stannic chloride is made by the direct chlorination of tin at 110—115°C. Any stannous chloride formed in the process is separated from the stannic chloride by volatilization and subsequently chlorinated to stannic chloride. The latter is inert to steel in the absence of moisture and is shipped in plain steel dmms of special design. Because prolonged contact with the skin causes bums, goggles and protective clothing should be used in the handling of stannic chloride. Stannic chloride, like stannous chloride, also forms many complexes (3). 

Zinn-bromwasserstoffsaure, /. bromostannic acid, -butter, /. (Old Chem.) butter of tin (stannic chloride), -charge, /. (Textiles) tin weighting, -chlorammonium, n. ammonium chlorostannate, (Dyeing) pink salt, -chlorid, n. tin chloride, specif, stannic chloride, tin (IV) chloride, -chloriir, n. stannous chloride, tin(II) chloride. 

Sodium i-nitro-2-naphtholate, 13, 78 Sodium perbenzoate, 13, 86 Sodium succinate, 12, 72 Sodium sulfide, 12, 68, 76 16, 72 Soxhlet extractor, 16, 69 17, 74 Stannic chloride, 18,1 Stannous chloride, 17, 10, 11 Steam distillation, rapid, 17, 20 Stilbene, 17, 90... 

Instead of copper one can use zinc, iron, stannous chloride, or cuprous chloride, the last-named two being oxidized to stannic and cupric chloride respectively. The reactions are carried out at low temperature ( — 10 to — 20°C) in acetone or ethyl acetate (Nesmeyanov et al., 1934 a). 

Sodium aluminium sulphate Sodium bisulphate Sodium hypochlorite Sodium perchlorate Sodium thiocyanate Stannic ammonium chloride Stannic chloride Stannous chloride Uranyl nitrate Zinc chloride Zinc fluorosilicate... 

B. Reduction of Dinitrodurene.—A solution of 90 g. of dini-trodurene in 1 1. of glacial acetic acid is boiled in a 12-I. flask (Note 6) 700 g. of stannous chloride is dissolved in 800 cc. of concentrated hydrochloric acid and heated to boiling. The heat is removed from the acetic acid solution of the nitro compound, and the stannous chloride solution is poured very carefully (during about ten minutes) into the dinitrodurene solution. The reaction is complete in fifteen minutes, and as the solution cools the stannic chloride compound of the diamine begins to crystallize. The reaction mixture is cooled to io° in an ice-water bath, and the solid is filtered off by suction, washed twice with 50 cc. of 95 per cent ethyl alcohol and twice with 50 cc. of ether, and dried. The filtrates from the tin compound contain very little of the reduction product and may be discarded. The composition of this compound is [G (CH i)4(NH2-HCI)2l2-SnCl4, and it crystallizes from the reaction mixture in fine, glistening plates which are almost colorless. The yield is 145 g. (97 per cent of the theoretical amount). 

Anhydrous sodium tungstate, 25 382 Anhydrous stannic chloride, 24 803 Anhydrous stannous chloride, 24 802-803 Anhydrous zinc chloride, 26 617 Anhydrous zinc sulfate, 26 617 Aniline, 2 783-809, 17 250, 259 alkylation, 2 197 Bechamp process, 2 490 from benzene, 3 619t, 620 chemical reactions, 2 783-789 derivatives, 2 783-809 economic aspects, 2 790-791... 

STANNIC BROMIDE STANNOUS CHLORIDE STANNIC CHLORIDE STANNIC HYDRIDE STANNIC IODIDE STRONTIUM STRONTIUM OXIDE TANTALUM TECNNETIUM TELLURIUM... 

Compounds Stannic oxide tin tetrachloride stannic chloride stannous chloride stannous sulfate sodium stannate potassium stannate... 

Anhydrous AnalaR stannous chloride was distilled from A into the electrolytic cell, C, under a high vacuum after the whole apparatus had been baked out. Vessel A was sealed off at X, the stannous chloride fused by the heater H, and a 12 V DC potential applied across the terminals Jj and T Tj led to a gas-carbon rod serving as anode, to a Pt wire cathode. Bubbles of stannic chloride vapour rose from the anode. The first runnings were pumped out and then the system was sealed off at Y. Electrolysis was continued until sufficient stannic chloride had been condensed in the sample holder, S, which was removed from the system by being sealed off at Z. 

Zinc chloride is much less reactive than aluminum chloride and usually requires higher reaction temperatures. However, it has the advantage that, unlike aluminum chloride, it is less sensitive to moisture and can sometimes even be used in aqueous media.88 Concentrated aqueous solutions of ferric chloride, bismuth chloride, zinc bromide, stannous chloride, stannic chloride, and antimony chloride are also alkylation catalysts, particularly in the presence of hydrochloric acid.89... 

A soft, almost silver-white metal, melting at 231° C. Tin dissolves in hot hydrochloric acid with the formation of stannous chloride. Hot concentrated nitric acid converts it into insoluble meta-stannic acid. 

Concentrated hydrochloric acid also dissolves the trichloride, about 100 g. of the latter dissolving in 1 litre of acid at 100° C.7 Dissolution in hydriodic acid is accompanied by evolution of heat and the triiodide is formed.8 Ethyl iodide reacts similarly.9 Double decomposition reactions occur w hen arsenic trichloride is heated with phosphorus triiodide, stannic iodide or germanium iodide, the reactions being complete.10 Similarly, potassium iodide heated with arsenic trichloride in a sealed tube at 210° C., and potassium bromide at 180° to 200° C., form respectively arsenic triiodide and tribromide.11 Stannous chloride, added to the solution in hydrochloric acid, causes reduction to arsenic (see p. 29). Arsenic trichloride may be completely separated from germanium chloride by extraction with concentrated hydrochloric acid.12 Ammonium, sodium and cobaltic chlorides react with arsenic trichloride to form additive compounds with magnesium, zinc and chromic chlorides there is no reaction.13... 

Tin forms dihahdes and tetrahahdes with all of the common halogens. These compounds may be prepared by direct combination of the elements, the tetrahalides being favored. Like the halides of tile lower main group 4 elements, all are essentially covalent. Their hydrolysis requires, therefore, an initial step consisting of the coordinative addition of Iwo molecules of water, followed by the loss of one molecule of HX. the process being repeated until the end product ft S111 Oil c is obtained. The most significant commercial tin halides are stannous chloride, stannic chloride, and stannous fluoride. 

HC.CgH4.N( N)Cl. Its stannic chloride salt, [20HC.C6H4.N( N)CDSnCl4], col ndls, mp expl mildly on heating in a flame was prepd from 3-nitro-benzaldehyde, stannous chloride in coned HC1 and Na nitrite, as described in Refs 1 2 Refs I)Beil 16,538 2)F.Tiemann R.Ludwig,... 

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