Tetrasodium 3,3 ,3",3" -

Trypan Blue. 3,3 /(3,3 -DimetliyI/T,i -Mpfte i-yl] 4,4 -diyl)bisDirect Blue 14 C.l. 23850 3,3 -[(3,3 -dimethyl-4,4 -bipheny]ene)bis(azo)]bis-(5-amino-4-hydroxy-2,7-naphthalenedisulfonic acid) tetra-sodium salt tetrasodium 3,3 -[(3,3 -dimethyI-4,4 -biphen-ylene)bis(azo)]bi s(5 -amino. 4-hydroxy-2,7 -naphthal enedi-sulfonate) sodium ditolyl -diazobis - 8-amino-1 -naphthol-... 

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. 

Crystalline CaHPO 2H20 loses both water molecules in a single step at moderately elevated temperature or upon storage to yield the anhydrous salt. The presence of free moisture accelerates this dehydration, which results in anhydrous dicalcium phosphate, often as a hard mass. Addition of a few percent of tetrasodium pyrophosphate or trimagnesium phosphate, Mg2(P0 2> stabilizes the dihydrate. The mechanism, however, is not well understood. Nonetheless, these materials are used widely to stabilize CaHPO 2H20, particulady for toothpaste appHcations. 

Sodium Pyrophosphates. Known pyrophosphate compounds in the Na20—H2O—P20 system are given in Table 10. Commercially important sodium pyrophosphates include tetrasodium pyrophosphate (TSPP), Na4P20y, and disodium pyrophosphate, Na2H2P20y, commonly referred to as sodium acid pyrophosphate (SAPP). These are prepared industrially by thermal dehydration of disodium and monosodium orthophosphate, respectively. Tetrasodium pyrophosphate exists in five crystalline modifications, only one of which is stable at room temperature. 

TSPP is readily crystallised from water as the decahydrate between —0.4° and 79°C, and as the anhydrous salt above 79°C. The solubiUty of tetrasodium pyrophosphate is illustrated in Figure 8. The pH of a 1% solution is 10.2. TSPP is quite stable in alkaline medium but hydrolyses rapidly to orthophosphate under acid conditions. 

Fig. 8. Solubihties of sodium acid pyrophosphate and tetrasodium pyrophosphate.

Sodium tripolyphosphate is produced by calcination of an intimate mixture of orthophosphate salts containing the correct overall Na/P mole ratio of 1.67. The proportions of the two anhydrous STP phases are controlled by the calcination conditions. Commercial STP typically contain a few percent of tetrasodium pyrophosphate and some trimetaphosphate. A small amount of unconverted orthophosphates and long-chain polyphosphates also may be present. 

Chelants at concentrations of 0.1 to 0.2% improve the oxidative stabiUty through the complexation of the trace metal ions, eg, iron, which cataly2e the oxidative processes. Examples of the chelants commonly used are pentasodium diethylenetriarninepentaacetic acid (DTPA), tetrasodium ethylenediarninetetraacetic acid (EDTA), sodium etidronate (EHDP), and citric acid. Magnesium siUcate, formed in wet soap through the reaction of magnesium and siUcate ions, is another chelant commonly used in simple soap bars. 

Tetrasodium pyrophosphate [7722-88-5] Na4P20y, is another important primary builder and detergent. In sequestration, it is not quite as effective as sodium tripolyphosphate and its usage in heavy-duty laundry powders has declined in recent years. Functionally, tetrasodium pyrophosphate is both a builder for surfactants (ie, water softener) and alkaH. 

EDA reacts with formaldehyde and sodium cyanide under the appropriate alkaline conditions to yield the tetrasodium salt of ethylenediaminetetraacetic acid (24). By-product ammonia is removed at elevated temperatures under a partial vacuum. The free acid or its mono-, di-, or trisodium salts can be produced by the appropriate neutrali2ation using a strong mineral acid. This same reaction with other amines is used to produce polyamino acetic acids and their salts. These products are used widely as chelating agents. 

Condensed Phosphates. The term condensed phosphate refers to any dehydrated, condensed orthophosphate for which the M20 P20 ratio is less than 3 1 (17). (1) is disodium orthophosphate [7558-79-4] and (2) tetrasodium pyrophosphate [7722-88-5]. 

Scouring may be conducted on jigs, boil-off machines, or kettles, depending on fabric weight, constmction, and crease tendency ia the rope form. A combination of a synthetic detergent and soda ash is usually used and scouring is conducted at 85—100°C. Certain nylon blends may require less stringent conditions and the use of less alkaline builders, such as tetrasodium pyrophosphate. 

Cellulose Diacetate. When preparing cellulose diacetate for dyeing, strong alkahes must be avoided in the scouring of acetate because the surface of the cellulose acetate would be saponified by such treatment. Many fabrics tend to crease and therefore requke open-width handling. Scouring is frequendy carried out on a jig or beam using 1.0 g/L of surfactant and 0.5—1.0 g/L tetrasodium pyrophosphate for 30 min at 70—80°C. 

Elastomeric Fibers. Elastomeric fibers are polyurethanes combiaed with other nonelastic fibers to produce fabrics with controlled elasticity (see Fibers, elastomeric). Processing chemicals must be carefully selected to protect all fibers present ia the blend. Prior to scouriag, the fabrics are normally steamed to relax uneven tensions placed on the fibers duriag weaving. Scouriag, which is used to remove lubricants and siting, is normally conducted with aqueous solutions of synthetic detergents and tetrasodium pyrophosphate, with aqueous emulsions of perchloroethylene or with mineral spidts and sodium pyrophosphate. 

A novel method for preparing amino heterocycles is illustrated by the preparation of 2-amino-5-methylthiophene (159). In this approach vinyl azides act as NH2 equivalents in reaction with aromatic or heteroaromatic lithium derivatives (82TL699). A further variant for the preparation of amino heterocycles is by azide reduction the latter compounds are obtained by reaction of lithio derivatives with p- toluenesulfonyl azide and decomposition of the resulting lithium salt with tetrasodium pyrophosphate (Scheme 66) (82JOC3177). 

Tetrasodium pyrene-l,3,6,8-tetrasulfonate [59572-10-0] M 610.5. Recrystd from aqueous acetone [Okahata et al. J Am Chem Soc 108 2863 1986]. 

Nicotinamide adenine dinucleotide phosphate reduced tetrasodium salt (reduced diphosphopyridine nucleotide phosphate sodium salt, NADPH) [2646-71-1] M 833.4, pK as for NADP. Mostly similar to NADH above. 

Tetrasodium EDTA, 127 Tetrasodium pyrophosphate, 127 TETRA Technologies Inc., 250 Teti-yl, 127... 

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