Agent, reducing, hydrazine

Scavenger including primary amines, hydrazines, reducing agents Scavenger for scavenger titanium (IV) chloride, titanium (IV) isoproposide, boronic acids... 

In aqueous solution hydrazine can behave either as an oxidising or reducing agent. Powerful reducing agents such as zinc reduce hydrazine to ammonia, while chlorine oxidises it to give nitrogen. 

This can be extracted from impure phosphine prepared by the action of sodium hydroxide on phosphorus. Unlike hydrazine, it has no basic properties. It is a powerful reducing agent and burns spontaneously in air, this reaction explaining why impure phosphine containing traces of diphosphane ignites spontaneously in air. 

Reductions. Hydrazine is a very strong reducing agent. In the presence of oxygen and peroxides, it yields primarily nitrogen and water with more or less ammonia and hydrazoic acid [7782-79-8]. Based on standard electrode potentials, hydrazine in alkaline solution is a stronger reductant than sulfite but weaker than hypophosphite in acid solution, it falls between and Ti ( 7). 

Nitrite can be deterrnined by reaction with sulfanilamide to form the diazo compound, which couples with /V-(1-naphthyl)ethylenediamine dihydrochloride to form an intensely colored red azo dye. Nitrate can be deterrnined in a similar manner after reduction to nitrite. Suitable reducing agents are cadmium filings or hydrazine. This method is useful at a nitrogen concentration of 10 -lO " M. 

Chromium Removal System. Chlorate manufacturers must remove chromium from the chlorate solution as a result of environmental regulations. During crystallization of sodium chlorate, essentially all of the sodium dichromate is recycled back to the electrolyzer. Alternatively, hexavalent chromium, Cr, can be reduced and coprecipitated in an agitated reactor using a choice of reducing agents, eg, sodium sulfide, sulfite, thiosulfate, hydrosulfite, hydrazine, etc. The product is chromium(III) oxide [1333-82-0] (98—106). Ion exchange and solvent extraction techniques have also... 

Pyrroline-N-oxides (12) are sometimes isolated when using zinc-ammonium chloride (19,20), iron-sulfuric acid (14) or hydrazine-Raney nickel (21) as reducing agents. During the reduction, dimerization has been often observed (22). 

The available studies indicate that diimide has been used as a reducing agent for the preparation of HNBR. It has been used mainly as an alternative for hydrogenation of nitrile rubber latex. The use of diimide to hydrogenate low-molecular weight olefines is well known in the organic literature [93]. Diimide can be conveniently generated in situ by thermal treatment of solutions of p-tolu-enesulfonyl hydrazide or oxidation of hydrazine. 

A colorless, fuming liquid miscihle with water, hydrazine (diazine) is a weak base but a strong reducing agent. Hydrazine is used as a rocket fuel because its combustion is highly exothermic and produces 620 KJ/mol ... 

Principles The reduction reaction is controlled essentially by the usual kinetic factors such as concentration of reactants, temperature, agitation, catalysts, etc. Where the reaction is vigorous, as, for example, when a powerful reducing agent like hydrazine is used, wasteful precipitation of A/, may occur throughout the whole plating solution followed by deposition on all exposed metallic and non-metallic surfaces which can provide favourable nucleation sites. In order to restrict deposition and aid adhesion, the selected areas are pre-sensitised after cleaning the sensitisers used are often based on noble metal salts. 

Functional biaryl derivatives are important industrial chemicals. They are used as monomers for the production of high performance and other polymers, as well as dyes, pharmaceuticals and agrochemical intermediates. We have developed an improved method for the dehalogeno-dimerization of aryl bromides to yield biaryl derivatives under mild conditions (temperature < 100°C, atmospheric pressure) using a common base, a 5 % Pd/C catalyst (0.1 - 10 % w/w, based on the starting material) in an aqueous medium and formyl hydrazine as the reducing agent. Several examples of biaryl derivatives are discussed. 

Sulfinic acids can be prepared by reduction of sulfonyl chlorides. Though mostly done on aromatic sulfonyl chlorides, the reaction has also been applied to alkyl compounds. Besides zinc, sodium sulfite, hydrazine, sodium sulfide, and other reducing agents have been used. For reduction of sulfonyl chlorides to thiols, see 19-57. 

The initial product is a salt of hydrazinesulfonic acid, which is converted to the hydrazine by acid treatment. Diazonium salts can also be reduced to arenes (14-24). N-Nitrosoamines can be denitrosated to secondary amines by a number of reducing agents, including H2 and a catalyst, BF3—THF—NaHC03, and NaBH4— TiCU, as well as by hydrolysis. ... 

Disulfides can be reduced to thiols by mild reducing agents, such as zinc and dilute acid or Ph3P and H2O. The reaction can also be aceomplished simply by heating with alkali. Among other reagents used have been LiAlR, Mg/ MeOH, KBH(0—i-Pr)3, and hydrazine or substituted hydrazines. ... 

Templates made of surfactants are very effective in order to control the size, shape, and polydispersity of nanosized metal particles. Surfactant micelles may enclose metal ions to form amphiphilic microreactors (Figure 11a). Water-in-oil reverse micelles (Figure 11b) or larger vesicles may function in similar ways. On the addition of reducing agents such as hydrazine nanosized metal particles are formed. The size and the shape of the products are pre-imprinted by the constrained environment in which they are grown. 

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