Hydrazine | Chemical Compound - Encyclopedia Britannica

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  • NIST Chemistry WebBook - Hydrazine
  • New Jersey Department of Health - Hazardous Substance Fact Sheet - Hydrazine
  • Agency for Toxic Substances and Disease Registry - Hydrazine
  • University of Bristol - School of Chemistry - Hydrazine
  • United States Environmental Protection Agency - Hydrazine
  • National Center for Biotechnology Information - Hydrazine Toxicology
  • NOAA Cameo Chemicals - Hydrazine
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hydrazine, (N2H4), one of a series of compounds called hydronitrogens and a powerful reducing agent. It is used in the synthesis of various pesticides, as a base for blowing agents that make the holes in foam rubber, and as a corrosion inhibitor in boilers. Hydrazine is a colourless liquid with an ammonia-like odor. It has a melting point of 2.0° C (35.6° F) and a boiling point of 113.5° C (236.3° F). It readily absorbs moisture to form the hydrate N2H4·H2O.

Hydrazine was first isolated from organic compounds in 1887. The common method of preparation is by the Raschig process, which involves the oxidation of ammonia with sodium hypochlorite in the presence of gelatin or glue. (Other variations of this process substitute urea for ammonia.)

Hydrazine reacts with acids and some metallic salts, and the products are used in the manufacture of certain explosives and agricultural fungicides. Hydrazine reacts with organic compounds to form alkyl hydrazines, used as fuel in rocket and jet propulsion. Other reactions with organic compounds yield hydrazones and hydrazides, which are used in such pharmaceuticals as isoniazid (in the treatment of tuberculosis) and as chemical intermediates in the production of polymers and photographic chemicals.

Ammonia and amines have a slightly flattened trigonal pyramidal shape with a lone pair of electrons above the nitrogen. In quaternary ammonium ions, this area is occupied by a fourth substituent. More From Britannica ammonia: Hydrazine

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