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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can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou
It is an intermediate in some hydrazine manufacturing processes. Synthesis. Acetone azine can be prepared from acetone and hydrazine: [3] 2 (CH 3) 2 CO + N 2 H 4 → ...
DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.
Alkyl hydrazones are 10 2 - to 10 3-fold more sensitive to hydrolysis than analogous oximes. [10] When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [11] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction.
Ketazines are also important intermediates in the industrial production of hydrazine hydrate by the peroxide process. [3] In the presence of an oxidant, ammonia and ketones react to give hydrazine via ketazine: 2 Me(Et)C=O + 2 NH 3 + H 2 O 2 → Me(Et)C=NN=C(Et)Me + 2 H 2 O. The ketazine can be hydrolyzed to the hydrazine and regenerate the ketone:
In 1935, Hellmuth Walter discovered that hydrazine hydrate was hypergolic with high-test peroxide of 80–83%. He was probably the first to discover this phenomenon, and set to work developing a fuel. Prof. Otto Lutz assisted the Walter Company with the development of C-Stoff which contained 30% hydrazine hydrate, 57% methanol , and 13% water ...
An applied example is a synthesis of sunitinib begins by mixing 5-fluoroisatin slowly into hydrazine hydrate. [9] After 4 hours at 110 °C, the indole ring structure has been broken into (2-amino-5-fluoro-phenyl)-acetic acid hydrazide with reduction of the ketone at the 3-position.