Sodium bis

EDA reacts readily with two moles of CS2 in aqueous sodium hydroxide to form the bis sodium dithiocarbamate. When aqueous ammonia and 2inc oxide (or manganese oxide or its hydrate) is used with a basic catalyst, the 2inc (or manganese) dithiocarbamate salt is isolated. Alternatively, the disodium salt can react with ZnSO or MnSO followed by dehydration in an organic solvent to yield the same salts (48—50). 

Sulfur Compounds. EDA reacts readily with two moles of CS- in aqueous sodium hydroxide to lonn Ihc bis sodium dithiocarbamate. 

Khodorov BI. Sodium inactivation and drug-induced immobilization of the gating charge in nerve membrane. Prog Biophys Mol Biol 1981 37 49-89. 

An MMA dimer obtained by CCT was hydrolyzed and then re-esterified with 1,10-decanediol. The resulting diester was allowed to react with chlorosulfonic acid to produce the methacrylate dimer surfactant, 2,4-bis(sodium 10-sulfate decanoxycarbonyl)-4-methyl-pent-l-ene. At the beginning of a polymerization, the molecule acts as a surfactant and subsequent incorporation of the dimer in the polymerization yields a surfactant-functionalized polymer. Thus, additional surfactants are not required. 

A copolymer was obtained on reaction of 1,1 -bis(iodomethyl)cyclopropane with the bis(sodium alkoxide) of hexane-1,6-diol. ... 

The parent pteridine can be obtained by condensing pyrimidine-4,5-diamine with glyoxal, either as its bis(sodium hydrogen sulfite) monohydrate,37 39 as its crude polymer in ethanol,37 or as its hydrated polymer in ethanol.40 This last method gives the best yield (93%). 

Eormation of stoichiometric HAp (stHAp) via an acid-base reaction between TTCP and acidic calcium phosphate (e.g., CaHP04, DCPA) in the presence of poly[bis(sodium carboxylatophenoxy) phosphazene (Na-PCPP) and poly[bis(potassium carboxylatophenoxy) phosphazene (K-PCPP) at 37.4 and 50°C was also investigated. Inhibition of stHAp formation depends on the proportion of polymer used and on temperature. Moreover, to minimize the inhibition of formation of HAp, it was suggested that lower molecular weight polymers be used [189]. 

TenHuisen KS, Brown PW, Reed CS et al (1996) Low temperature synthesis of a selfassembling composite Hydroxyapatite-poly[bis(sodium carboxylatophenoxy) phosphazenel. J Mater Sci Mater Med 7 763-782... 

Difluorodiphenyl. Bis-diazotise a solution of 46 g. of benzidine (Section IV,88) in 150 ml. of concentrated hydrochloric acid and 150 ml. of water by means of a solution of 35 g. of sodium nitrite in 60 ml. of water add about 200 g. of crushed ice during the process (compare p-Fbtorotoluene above). Filter the solution and add it to a filtered solution of 85 g. of sodium borofluoride in 150 ml. of water. Stir for several minutes, collect the precipitated bis-diazonium borofluoride by suction filtration, wash with 5 ml. of ice-cold water, and dry at 90-100°. Place the dry salt in a flask fitted with an air condenser, immerse the flask in an oil bath, and slowly raise the temperature to 150° (Fume Cupboard ). When decomposition of the salt is complete, steam distil the mixture collect the 4 4 difluoro-diphenyl which passes over and recrystallise it from ethanol. The yield is 21 g., m.p. 92-93°. 

Step 2. Distillation from alkaline solution. Treat the solution Bi) remaining in the distilling flask after the volatile acidic and neutral compounds have been removed with 10-20 per cent, sodium hydroxide solution until distinctly alkaline. If a solid separates, filter it off and identify it. Distil the alkaline solution until no more volatile bases pass... 

Cumulenic ethers with the 4-positions blocked by alkyl groups can be obtained from bis-ethers, R0-CH2C=C-C(R )(r2)0R, and sodium amide in liquid NHj, applying the... 

If alkyl groups are attached to the ylide carbon atom, cis-olefins are formed at low temperatures with stereoselectivity up to 98Vo. Sodium bis(trimethylsilyl)amide is a recommended base for this purpose. Electron withdrawing groups at the ylide carbon atom give rise to trans-stereoselectivity. If the carbon atom is connected with a polyene, mixtures of cis- and rrans-alkenes are formed. The trans-olefin is also stereoseiectively produced when phosphonate diester a-carbanions are used, because the elimination of a phosphate ester anion is slow (W.S. Wadsworth, 1977). 

Treating 5.5 g of 2-amino-4,5-dimethylthiazole HCl with 0.66 g of solid sodium hydroxide 15 min at 220°C yields 53% of 4.4. 5.5 -tetramethyT 2,2 -dithiazolylamine, whose structure w as proved by identification with the produa obtained from the reaction between dithiobiuret and 3-bromo-2-butanone (467). This result is comparable to the reaction between 2-aminopyridine and its hydrochloride to yield bis(pyridyl-2)amine (468). Gronowitz applied this reaction to 2-aminothiazole, refluxing it with its hydrochloride 4 hr in benzene and obtained the dimeric 2-aminothiazole (236). He proposed a mechanism (Scheme 143) that involves the addition of a proton to the 5-position of the ring to give 234. The carbocation formed then reacts on the 5-position of a second... 

Thus reduction of the 5-thiocyanato group of 151 by zinc (333, 360, 361) or aqueous sodium sulfide (348. 362), hydrolysis of the thiouronium group (7, 363, 364), and deacetylation of the 5-acetylthiothiazole with cold piperidine (365) have been performed to yield the 5-mercapto-thiazole (Scheme 78). It must be pointed out that depending on the experimental conditions, bis(5-thiazolyl(sulfide may be observed as a byproduct (363, 365). Thus 5-amino-4-methylthiazole (152) treated with... 

Other sulfur compounds such as thiourea, ammonium dithiocarbamate, or hydrogen sulfide also lead to 2-mercaptothiazoles. Thus thiourea has been used in the syntheses of 4,5-dimethyl (369) and 4-aryl-2-mercapto-thiazoles (Table 11-30) (519). The reactions were carried out by condensing the ia -thiocyanatoketones with thiourea in alcohol and water acidified with hydrochloric acid. By this procedure, 4-aryl-2-mercaptothiazoles were obtained in yields of 40 to 80% with bis-(4-aryl-2-thiazolyl) sulfides as by-products (519). These latter products (194) have also been observed as a result of the action of thiourea on 2-chloro-4-arylthiazole under the same experimental conditions. They can be separated from 2-mercaptothiazoles because of their different degrees of solubility in sodium hydroxide solution at 5%. In this medium bis-(4-phenyl-2-thiazolyl)sulfide is... 

The systematic name for bi carbonate ion is hydrogen carbonate Thus the system atic name for sodium bicar bonate (NaHCOs) is sodium hydrogen carbonate... 

Description of Method. The water-soluble vitamins Bi (thiamine hydrochloride), B2 (riboflavin), B3 (niacinamide), and Be (pyridoxine hydrochloride) may be determined by CZE using a pH 9 sodium tetraborate/sodlum dIhydrogen phosphate buffer or by MEKC using the same buffer with the addition of sodium dodecyl-sulfate. Detection Is by UV absorption at 200 nm. An Internal standard of o-ethoxybenzamide Is used to standardize the method. 

The order of elution when using MEKC is vitamin B3 (5.58 min), vitamin Be (6.59 min), vitamin 82 (8.81 min), and vitamin Bi (11.21 min). What conclusions can you make about the solubility of the B vitamins in the sodium dodecylsulfate micelles ... 

Some elements (S, Se, Te, P, As, Sb, Bi, Ge, Sn, Pb) are conveniently converted into their volatile hydrides before passed into the plasma. The formation of the hydrides by use of sodium tetrahydroborate (sodium borohydride) can be batchwise or continuous. 

Bis (trimethyl silyl) peroxide (CH2)3SiOOSi(CH2)3 can be used with triflic acid (CF SO H) and acts as an effective hydroxylating agent of aromatics such as toluene, mesitylene and naphthalene (165). Sodium perborate (a safe and inexpensive commercial chemical) can be used in conjunction with the triflic acid to hydroxylate aromatics (166). 

Phenolphthalein. Alophen, Ex-Lax, Feen-a-Miat, Modane, and Phenolax are trade names for phenolphthaleia [77-09-8] (3,3-bis(4-hydroxyphen5l)-l-(3ff)-l isobensofuranone) (10). It is a white or faintiy yellowish white crystalline powder, odorless and stable ia air, and practically iasoluble ia water one gram is soluble ia 15 mL alcohol and 100 mL diethyl ether. Phenolphthaleia may be prepared by mixing phenol, phthaHc anhydride, and sulfuric acid, and heating at 120°C for 10—12 h. The product is extracted with boiling water, then the residue dissolved ia dilute sodium hydroxide solution, filtered, and precipitated with acid. 

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