Phenylhydrazine CAS#100-63-0
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Chemical Name:Phenylhydrazine
CAS No.:100-63-0
Molecular Formula:C6H8N2
Molecular weight:108.14
Sample: Available
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Products Description of Phenylhydrazine CAS#100-63-0
Phenylhydrazine, also known as hydrazine, was first synthesized by German organic chemist Hermann Emil Fischer in 1875 and is the first synthesized hydrazine derivative. It is a light yellow crystal or oily liquid at room temperature and a monoclinic prism crystal at low temperature. It is easily oxidized in the air and becomes dark brown or dark red. It is one of the derivatives of hydrazine, often abbreviated as PhNHNH2. It is slightly soluble in water and alkaline solution, and soluble in dilute acid. It is miscible with ethanol, ether, chloroform and benzene.
The common preparation method is to generate diazonium salt by reacting aniline with sodium nitrite under the action of hydrochloric acid, and then reduce it with sodium sulfite/sodium hydroxide. Phenylhydrazine hydrochloride is generated by acid precipitation, and phenylhydrazine is obtained after neutralization. It is used to make dyes, drugs, developers, etc. It is also an important reagent for identifying carbonyl groups, used to identify aldehydes, ketones and sugars. It reacts with benzaldehyde to form phenylhydrazone, and the hydrazone formed by phenylhydrazine or 2,4-dinitrophenylhydrazine is used to identify aldehydes and ketones. It reacts with aldehydes and ketones in the Fischer indole synthesis (discovered by Hermann Emil Fischer in 1883. The reaction is to use phenylhydrazine and aldehydes and ketones to heat and rearrange under acid catalysis to eliminate a molecule of ammonia to obtain 2- or 3-substituted indoles.) to obtain indole ring compounds.
Phenylhydrazine Chemical Properties
Melting point | 18-21 °C (lit.) |
Boiling point | 238-241 °C (lit.) |
density | 1.098 g/mL at 25 °C (lit.) |
vapor density | 4.3 (vs air) |
vapor pressure | <0.1 mm Hg ( 20 °C) |
refractive index | n20/D 1.607(lit.) |
Fp | 192 °F |
storage temp. | Store below +30°C. |
solubility | Soluble in dilute acids. |
form | Powder |
pka | 8.79(at 15℃) |
color | White to slightly blue or light beige |
explosive limit | 1.1%(V) |
Water Solubility | 145 g/L (20 ºC) |
Sensitive | Air & Light Sensitive |
Merck | 14,7293 |
BRN | 606080 |
Exposure limits | TLV-TWA skin 0.1 ppm (0.44 mg/m3) (ACGIH), 5 ppm (22 mg/m3) (OSHA); STEL 10 ppm (44 mg/m3) (OSHA); carcinogenicity: A2-Suspected Human Carcinogen (ACGIH), Carcinogen (NIOSH). . |
Dielectric constant | 7.2(23℃) |
Stability: | Stable, but may decompose in sunlight. May be air or light sensitive. Incompatible with strong oxidizing agents, metal oxides. |
CAS DataBase Reference | 100-63-0(CAS DataBase Reference) |
NIST Chemistry Reference | Hydrazine, phenyl-(100-63-0) |
EPA Substance Registry System | Phenylhydrazine (100-63-0) |
Safety Information
Hazard Codes | T,N |
Risk Statements | 45-23/24/25-36/38-43-48/23/24/25-50-68 |
Safety Statements | 53-45-61 |
RIDADR | UN 2572 6.1/PG 2 |
WGK Germany | 3 |
RTECS | MV8925000 |
F | 8-10-23 |
Autoignition Temperature | 345 °F |
TSCA | Yes |
HS Code | 2928 00 90 |
HazardClass | 6.1 |
PackingGroup | II |
Hazardous Substances Data | 100-63-0(Hazardous Substances Data) |
Toxicity | LD50 orally in Rabbit: 188 mg/kg |
IDLA | 15 ppm |
Product Application of Phenylhydrazine CAS#100-63-0
Phenylhydrazine is used in the production of pesticides to synthesize the intermediate 1-phenylaminourea of the organophosphorus insecticide triazophos and the intermediate 1-phenyl-3,6-dihydroxypyridazine of pyridazinon. It is also the intermediate of the new fungicide faChemicalbookmoxadone and fenamidone. In addition, as an organic synthesis raw material, phenylhydrazine is also used as an intermediate in the dye, pharmaceutical and other industries, and is also used as an analytical reagent.
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