Hydrazine
|
| |||
|
| |||
Anhydrous hydrazine | |||
| Names | |||
|---|---|---|---|
| IUPAC name
Hydrazine | |||
| Systematic IUPAC name
Diazane | |||
| Other names
Diamine Tetrahydridodinitrogen(N-N) Diamidogen | |||
| Identifiers | |||
3D model (JSmol) |
|||
| 3DMet | |||
| 878137 | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.005.560 | ||
| EC Number |
| ||
| 190 | |||
| KEGG | |||
| MeSH | Hydrazine | ||
PubChem CID |
|||
| RTECS number |
| ||
| UNII | |||
| UN number | 2029 | ||
CompTox Dashboard (EPA) |
|||
| |||
| |||
| Properties | |||
| N2H4 | |||
| Molar mass | 32.0452 g/mol | ||
| Appearance | Colorless, fuming, oily liquid | ||
| Odor | Ammonia-like | ||
| Density | 1.021 g/cm3 | ||
| Melting point | 2 °C; 35 °F; 275 K | ||
| Boiling point | 114 °C; 237 °F; 387 K | ||
| Miscible | |||
| log P | 0.67 | ||
| Vapor pressure | 1 kPa (at 30.7 °C) | ||
| Acidity (pKa) | 8.10 ([N2H5]+) | ||
| Basicity (pKb) | 5.90 | ||
| Conjugate acid | Hydrazinium | ||
Refractive index (nD) |
1.46044 (at 22 °C) | ||
| Viscosity | 0.876 cP | ||
| Structure | |||
| Triangular pyramidal at N | |||
| 1.85 D | |||
| Thermochemistry | |||
Std molar entropy (S⦵298) |
121.52 J/(K·mol) | ||
Std enthalpy of formation (ΔfH⦵298) |
50.63 kJ/mol | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H226, H301, H311, H314, H317, H331, H350, H410 | |||
| P201, P261, P273, P280, P301+P310, P305+P351+P338 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | 52 °C (126 °F; 325 K) | ||
| 24 to 270 °C (75 to 518 °F; 297 to 543 K) | |||
| Explosive limits | 1.8–100% | ||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
59–60 mg/kg (oral in rats, mice) | ||
LC50 (median concentration) |
260 ppm (rat, 4 hr) 630 ppm (rat, 1 hr) 570 ppm (rat, 4 hr) 252 ppm (mouse, 4 hr) | ||
| NIOSH (US health exposure limits): | |||
PEL (Permissible) |
TWA 1 ppm (1.3 mg/m3) [skin] | ||
REL (Recommended) |
Ca C 0.03 ppm (0.04 mg/m3) [2-hour] | ||
IDLH (Immediate danger) |
Ca [50 ppm] | ||
| Safety data sheet (SDS) | ICSC 0281 | ||
| Related compounds | |||
Other anions |
Tetrafluorohydrazine Hydrogen peroxide Diphosphane Diphosphorus tetraiodide | ||
Other cations |
Organic hydrazines | ||
Related Binary azanes |
Ammonia Triazane | ||
Related compounds |
Diazene Triazene Tetrazene Diphosphene | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Hydrazine is an inorganic compound with the chemical formula N2H4. It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour. Hydrazine is highly toxic unless handled in solution as, for example, hydrazine hydrate (N2H4·xH2O).
Hydrazine is mainly used as a foaming agent in preparing polymer foams, but applications also include its uses as a precursor to pharmaceuticals and agrochemicals, as well as a long-term storable propellant for in-space spacecraft propulsion. Additionally, hydrazine is used in various rocket fuels and to prepare the gas precursors used in air bags. Hydrazine is used within both nuclear and conventional electrical power plant steam cycles as an oxygen scavenger to control concentrations of dissolved oxygen in an effort to reduce corrosion. As of 2000, approximately 120,000 tons of hydrazine hydrate (corresponding to a 64% solution of hydrazine in water by weight) were manufactured worldwide per year.
Hydrazines are a class of organic substances derived by replacing one or more hydrogen atoms in hydrazine by an organic group.