Phenylhydrazine

[5] Phenylhydrazine forms monoclinic prisms that melt to an oil around room temperature which may turn yellow to dark red upon exposure to air.

[1] Phenylhydrazine is miscible with ethanol, diethyl ether, chloroform and benzene.

[6] Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875.

[9] This molecule is also used to induce acute hemolytic anemia in animal models.

Exposure to phenylhydrazine may cause contact dermatitis, hemolytic anemia, and liver damage.

Phenylhydrazine
Phenylhydrazine
Ball-and-stick model of phenylhydrazine
Ball-and-stick model of phenylhydrazine
Space-filling model of phenylhydrazine
Space-filling model of phenylhydrazine
NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide Special hazards (white): no code