| Molecular Formula | C6H7NO |
| Molar Mass | 109.13 |
| Density | 1.1143 (rough estimate) |
| Melting Point | 80-84℃ |
| Boling Point | 204.59°C (rough estimate) |
| Flash Point | 120.2°C |
| Water Solubility | 20g/L(5 ºC) |
| Vapor Presure | 0.085mmHg at 25°C |
| pKa | 9.00±0.70(Predicted) |
| Storage Condition | -20°C |
| Stability | Unstable - deteriorates with storage. Incompatible with strong oxidizing agents. |
| Refractive Index | 1.5444 (estimate) |
| Physical and Chemical Properties | Yellow needle-like crystals. Melting Point 81-82 °c. Spontaneous explosion. |
| Hazard Symbols | T - Toxic![]() |
| Risk Codes | 25 - Toxic if swallowed |
| Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2811 |
| WGK Germany | 3 |
| RTECS | NC4900000 |
| Hazard Class | 6.1 |
| Packing Group | Ⅲ |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| use | for organic synthesis. |
| production method | 250g(4.7mol) of nitrobenzene and 8L of water are vigorously stirred together, 620g(8.1mol) of 85% zinc powder are added in batches within 15-20min, the temperature in the reduction reaction is raised to 60-65 ℃, the reaction is completed, zinc oxide is filtered out while hot, the filtrate is saturated with salt (about 3kg of salt is required), and cooled to 0 ℃, crystallize out phenylhydroxylamine. The pure product was 275-300g with a yield of 62-68%. |
| toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |