hydrazine

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hydrazine

(hī`drəzēn'), chemical compound, formula NH2NH2, m.p. 1.4°C;, b.p. 113.5°C;, specific gravity 1.011 at 15°C;. It is very soluble in water and soluble in alcohol. At ordinary temperatures it is a colorless, fuming liquid that has an ammonialike odor, but when frozen it forms white crystals. Hydrazine is corrosive and a strong reducing agent, but it is a weaker base than ammoniaammonia,
chemical compound, NH3, colorless gas that is about one half as dense as air at ordinary temperatures and pressures. It has a characteristic pungent, penetrating odor.
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. It reacts with water to form hydrazine hydrate, N2H4·H2O, a colorless liquid that boils at 120°C;. Hydrazine can be prepared (usually as the hydrate) by reacting ammonia with chloramine, NH2Cl, in the presence of glue or gelatin. The glue or gelatin inhibits decomposition of the hydrazine. Ammonium chloride is a byproduct. The chloramine may be prepared by reacting ammonia with a hypochlorite or chlorine gas. Hydrazine is also prepared by reaction of sodium hypochlorite with urea in the presence of glue or gelatin. Hydrazine is dibasic and forms many salts, e.g., mono- and di-hydrochlorides, mono- and di-nitrates, and two sulfates. The major use of hydrazine is as a rocket fuel because it burns rapidly, producing a large amount of heat. Hydrazine and its derivatives are also used in the manufacture of algicides, fungicides, insecticides, and agricultural chemicals; in rubber curing and the manufacture of foam rubber and plastics; in soldering fluxes; and as a corrosion inhibitor in boiler feedwater. Isoniazidisoniazid
, drug used to treat tuberculosis. Also known as isonicotinic acid hydrazide, isoniazid is the most effective antituberculosis drug currently available. The drug inhibits or kills the tubercle bacilli that cause the disease.
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, a drug used in treatment of tuberculosis, is isonicotinic hydrazide.

Hydrazine

 

(also called diamide), H2N—NH2, a colorless, hygroscopic liquid that fumes in air. Boiling point, 113.5° C; melting point, 2° C; density, 1,008 g/cm3 (at 20° C). Hydrazine is absolutely soluble in water and low alcohols. It is insoluble in hydrocarbons and other organic solvents. Aqueous solutions of hydrazine are basic (KHydrazine = 8.5 x 10−7). With acids it forms salts of hydrazone, such as N2H5C1 and N2H6C12. Hydrazine is characterized by a high dielectric constant (52.9 at 20° C) and is able to dissolve many inorganic salts.

Hydrazine is an endothermal compound; heat of formation ΔHHydrazine (1) = 50.24 kilojoules per mole (12.05 kilocalories per mole). Upon heating to 200°-300° C, hydrazine decomposes to N2 and NH3. In the presence of Fe203, it ignites at room temperature. A mixture of hydrazine vapor with air at a content of 4.67 percent or more by volume forms an explosive mixture. Liquid hydrazine is not sensitive to impact, friction, or detonation. It is toxic; the maximum permissible concentration in air is 0.0001 mg/l. Hydrazine is produced by oxidation of NH3 or urea by hypochloride. It is used in organic synthesis, as a component of liquid rocket fuels, and in the production of plastics, cured rubber, insecticides, and explosives.

REFERENCE

Audrieth, L., and B. Ogg. Khimiia gidrazina. Moscow, 1954. (Translated from English.)

V. S. LAPIK

hydrazine

[′hī·drə‚zēn]
(inorganic chemistry)
H2NNH2 A colorless, hygroscopic liquid, boiling point 114°C, with an ammonialike odor; it is reducing, decomposable, basic, and bifunctional; used as a rocket fuel, in corrosion inhibition in boilers, and in the synthesis of biologically active materials, explosives, antioxidants, and photographic chemicals.
References in periodicals archive ?
In the case of an equimolar or 2/1 ratio of protected hydrazine and benzyl bromide, relatively poor yields ranging from 13% to 30% were obtained at room temperature.
It was important to consider that the type of the suitable base was dependent on the properties of the hydrazine protecting group.
In early hydrazine alkylation studies it was found that the use of ethanol as a solvent for hydrazine alkylation reaction helps to increase monoalkylated hydrazine yield [15].
The preliminary results seem to be very promising, thus giving a new opportunity for the synthesis of heteroaryl substituted hydrazines.
Synthetic methodology for alkyl substituted hydrazines.
A Convienient, one-pot preparative method for tri- and tetrasubstituted hydrazines from azobenzenes and organolithiums.
In this report we suggest an alternative synthesis of the aza-arginine precursor, using alkylation of N-protected hydrazine with N-protected 3-bromopropyl amine (Scheme 2), and thereafter converting the protected aza-ornithine precursor into a precursor of aza-arginine (Scheme 3).
omega]]-di-Boc-guanydil)propyl) hydrazine was prepared using the following procedure: N-Fmoc-N'-(3-(N-Boc)aminopropyl)hydrazine (5) was dissolved in DCM-TFA mixture (1 : 2) and stirred for 4 h at room temperature.
The dehydration of hydrazine hydrate, in contrast, is well known.
of the series of drying experiments it was confirmed that allyl hydrazine formed an extremely stable hydrate, which could not be decomposed with the traditional drying agents.
Hydrazine sulfate influence on nutritional status and survival in non-small-cell lung cancer (abstract), journal of Clinical Oncology.
Influence of hydrazine sulfate on abnormal carbohydrate metabolism in cancer patients with weight loss.