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Hydrazine sulfate is a useful salt that finds its use mainly in organic sythesis.  It was at one point thought to be effective at treating cancer, however this was disproven.

PropertiesEdit

ChemicalEdit

Hydrazine sulfate has the molecular formula N2H6SO4, however this is better represented as N2H5HSO4.  It finds uses in organic chemistry, mainly by forming hydrazides.

PhysicalEdit

Hydrazine sulfate is a white crystalline solid melting at 254°C.

AvailabilityEdit

Hydrazine sulfate is not very readily available for purchase to the amateur, but it is easily and cheaply made at home.

PreparationEdit

There are many ways in which an amateur can produce hydrazine sulfate.  Two important ones which give decent, around 50%, yields are shown below.

Hypochlorite-Ketazine ProcessEdit

Concentrated(20 - 30%) ammonia is mixed with methyl ethyl ketone and a few hundred mg of gelatin and cooled down to 0°C. Sodium hypochlorite is then added dropwise until the stoichiometric amount has been added.  A hydrophobic azine (methyl ethyl ketazine) which is less dense than water, will then separate.  This azine is then mixed with a stoichiometric amount of ~17% sulfuric acid, and heated to the boiling point of MEK to ensure full hydrolysis of the azine.  Finally, the solution is chilled to 0°C to precipitate the hydrazine sulfate.  The solution is then vacuum filtered.[1]

Hoffman Rearrangement of UreaEdit

A solution of 10% sodium hypochlorite is added to solid sodium hydroxide and the mixture is kept cold during the addition.  Meanwhile, a solution of urea with a few hundred mg of gelatin is prepared.  The two solutions are mixed and allowed to fully react, a voluminous foam will appear.  After they have reacted, MEK is added to the solution and the azine is processed as previoulsy described.[2]

ProjectsEdit

When mixed with a solution of silver nitrate, a silver mirror will be formed on the surface of the container.  Hydrazine sulfate also finds a variety of uses in organic syntheses such as the preparation of 2,4 dinitrophenylhydrazine, and the preparation of luminol.

SafetyEdit

Hydrazine sulfate is much safer than its free base, hydrazine.  However, it is still moderately toxic and a suspected carcinogen. It may ignite on contact with certain strong oxidizers.

ReferencesEdit

  1. https://www.youtube.com/watch?v=UB7vwIFCnR0
  2. https://www.youtube.com/watch?v=JCrDttuw5co

Relevant Sciencemadness threadsEdit

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