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Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).
Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou
Hydrazine – N 2 H 4; Hydrazoic acid – HN 3; Hydroiodic acid – HI; Hydrogen bromide – HBr; Hydrogen chloride – HCl; Hydrogen cyanide – HCN; Hydrogen fluoride – HF; Hydrogen peroxide – H 2 O 2; Hydrogen selenide – H 2 Se; Hydrogen sulfide – H 2 S; Hydrogen telluride – H 2 Te; Hydroxylamine – NH 2 OH; Hypobromous acid ...
Unsymmetrical dimethylhydrazine (abbreviated as UDMH; also known as 1,1-dimethylhydrazine, heptyl or Geptil) is a chemical compound with the formula H 2 NN(CH 3) 2 that is primarily used as a rocket propellant. [4]
Hydrazine sulfate, more properly hydrazinium hydrogensulfate, is a salt of the cation hydrazinium and the anion bisulfate (hydrogensulfate), ...
Industrially the compound is produced by treatment of urea with hydrazine: [3] OC(NH 2) 2 + 2 N 2 H 4 → OC(N 2 H 3) 2 + 2 NH 3. It can also be prepared by reactions of other C1-precursors with hydrazine, such as carbonate esters. [2] It can be prepared from phosgene, but this route cogenerates the hydrazinium salt [N 2 H 5]Cl and results in ...
Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...
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