Hydrazine

Hydrazine is the ammonia-like odor, hydrazine has a liquid range and density similar to water.

Molecular structure and properties

Conceptually, hydrazine arises via coupling a pair of anticlinal conformation, and also experiences a strong rotational barrier.

It has ammonia but 15 times weaker.

N₂H₄ + H⁺ → [N₂H₅]⁺ K = 8.5 x 10^-7

(for ammonia K = 1.78 x 10^-5) It can be diprotonated only with difficulty:^[3]

[N₂H₅]⁺ + H⁺ → [N₂H₆]²⁺ K = 8.4 x 10^-16

Synthesis

Theodor Curtius synthesized free hydrazine for the first time in 1889 via a circuitous route.^[4]

Hydrazine is produced in the Olin Raschig process from chloramine with ammonia.^[5]

In the Atofina-PCUK cycle, hydrazine is produced in several steps from hydrazone, a process that couples two nitrogen atoms. This hydrazone reacts with one more equivalent of acetone, and the resulting azine is hydrolyzed to give hydrazine, regenerating acetone. Unlike the Raschig process, this process does not produce salt. The PCUK stands for Produits Chimiques Ugine Kuhlmann, a French chemical manufacturer.^[6]

Hydrazine can also be produced via the so-called ketazine and peroxide processes.

In 2001, Microbiologist Marc Strous from the University of Nijmegen in the Netherlands discovered that hydrazine is produced from yeast bacteria and the open ocean bacterium anammox (Brocadia anammoxidans). They are the only discovered organisms to naturally produce hydrazine.^[7]

Hydrazine derivatives

Many substituted hydrazines are known, and several occur naturally. Some examples:

• gyromitrin and agaritine are phenylhydrazines found in the commercially produced mushroom species Agaricus bisporus. Gyromitrin is metabolized into monomethyl hydrazine.
• phenelzine are hydrazine-containing medications.
• methyl groups.
• organic chemistry.
• phenylhydrazine, C₆H₅NHNH₂, the first hydrazine to be discovered.

Uses in chemistry

Hydrazines are part of many organic syntheses, often those of practical significance in dyes and in photography.

Hydrazone formation

Illustrative of the condensation of hydrazine with a simple carbonyl is its reaction with azine. This azine reacts further with hydrazine to afford the hydrazone:^[8]

2 (CH₃)₂CO + N₂H₄ → 2 H₂O + [(CH₃)₂C=N]₂

[(CH₃)₂C=N]₂ + N₂H₄ → 2 (CH₃)₂C=NNH₂

The acetone azine is an intermediate in the Atofina-PCUK synthesis. Direct hydrazones to hydrazines present a clean way to produce 1,1-dialkylated hydrazines.

In a related reaction 2-cyanotriazines.

Wolff-Kishner reduction

Hydrazine is used in the dinitrogen from the hydrazine derivative helps to drive the reaction.

Heterocyclic chemistry

Being bifunctional, with two amines, hydrazine is a key building block for the preparation of many heterocyclic compounds via condensation with a range of difunctional electrophiles. With 2,4-pentanedione, it condenses to give the 3,5-dimethylpyrazole.^[9] In the Einhorn-Brunner reaction hydrazines react with imides to give triazoles.

Sulfonation

Being a good nucleophile, N₂H₄ is susceptible to attack by sulfonyl halides and acyl halides.^[10] The tosylhydrazine also forms hydrazones upon treatment with carbonyls.

Deprotection of phthalimides

Hydrazine is used to cleave N-alkylated phthalimide derivatives. This scission reaction allows phthalimide anion to be used as amine precursor in the Gabriel synthesis.^[11]

Reducing agent

Hydrazine is a convenient reductant because the by-products are typically nitrogen gas and water. Thus, it is used as an plutonium extraction from nuclear reactor waste.

Hydrazinium salts

Hydrazine is converted to solid salts by treatment with mineral acids. A common salt is hydrazine hydrogen hydrazoic acid N₅H₅ was of scientific interest, because of the high nitrogen content and the explosive properties.

Other industrial uses

Hydrazine is used in many processes including: production of ammonium nitrate.

Rocket fuel

Hydrazine was first used as a C-Stoff.

Hydrazine is also used as a low-power monopropellant for the maneuvering thrusters of spacecraft, and the Space Shuttle's Auxiliary Power Units. In addition, monopropellant hydrazine-fueled rocket engines are often used in terminal descent of spacecraft. A collection of such engines were used in both Viking landers as well as the Phoenix lander launched in August 2007.

In all hydrazine monopropellant engines the hydrazine is passed by a ammonia, nitrogen gas, and hydrogen gas according to the following reactions:

1. 3 N₂H₄ → 4 NH₃ + N₂
2. N₂H₄ → N₂ + 2 H₂
3. 4 NH₃ + N₂H₄ → 3 N₂ + 8 H₂

These reactions are extremely exothermic (the catalyst chamber can reach 800 °C in a matter of milliseconds^[12]), and they produce large volumes of hot gas from a small volume of liquid hydrazine,^[13] making it an efficient thruster propellant.

Other variants of Hydrazine that are used as rocket fuel are dinitrogen tetroxide, N₂O₄.

Safety

Hydrazine is highly toxic and dangerously unstable, especially in the anhydrous form. Symptoms of acute exposure to high levels of hydrazine may include irritation of the eyes, nose, and throat, dizziness, headache, nausea, pulmonary edema, seizures, and coma in humans. Acute exposure can also damage the liver, kidneys, and central nervous system in humans. The liquid is corrosive and may produce dermatitis from skin contact in humans and animals. Effects to the lungs, liver, spleen, and thyroid have been reported in animals chronically exposed to hydrazine via inhalation. Increased incidences of lung, nasal cavity, and liver tumors have been observed in rodents exposed to hydrazine.

References

See also

• List of Stoffs