| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
Methylhydrazine[1] | |
| Other names
Methyldiazane, monomethyl hydrazine | |
| Identifiers | |
| |
3D model (JSmol) |
|
| 635645 | |
| ChEMBL | |
| ChemSpider |
|
| ECHA InfoCard | 100.000.429 
|
| EC Number |
|
| MeSH | Monomethylhydrazine |
PubChem CID |
|
| RTECS number |
|
| UNII | |
| UN number | 1244 |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| CH6N2 | |
| Molar mass | 46.073 g·mol−1 |
| Appearance | Fuming, colourless liquid |
| Odor | Fish-like [2] |
| Density | 875 mg/mL (at 20 °C) |
| Melting point | −52 °C (−62 °F; 221 K) |
| Boiling point | 87.50 °C; 189.50 °F; 360.65 K |
| Miscible[3] | |
| log P | −1.318 |
| Vapor pressure | 5.00 kPa (at 20 °C) |
Refractive index (nD) |
1.4325 |
| Thermochemistry | |
Heat capacity (C) |
134.93 J/(K·mol) |
Std molar |
165.94 J/(K·mol) |
Std enthalpy of |
54.14 kJ/mol |
Std enthalpy of |
−1305.8 to −1304.6 kJ/mol |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
highly toxic and reactive liquid |
| GHS labelling: | |
   
| |
| Danger | |
| H225, H300, H301, H311, H314, H330, H351, H411 | |
| P210, P260, P273, P280, P284 | |
| NFPA 704 (fire diamond) | |
| Flash point | −8 °C; 17 °F; 265 K[3] |
| 196 °C (385 °F; 469 K) | |
| Explosive limits | 2.5–92%[3] |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
32 mg/kg (oral, rat) |
LC50 (median concentration) |
|
| NIOSH (US health exposure limits): | |
PEL (Permissible) |
C 0.2 ppm (0.35 mg/m3) [skin][3] |
REL (Recommended) |
Ca C 0.04 ppm (0.08 mg/m3) [2-hr][3] |
IDLH (Immediate danger) |
Ca [20 ppm][3] |
| Safety data sheet (SDS) | inchem.org |
| Related compounds | |
Related compounds |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Monomethylhydrazine (mono-methyl hydrazine, MMH) is a highly toxic, volatile hydrazine derivative with the chemical formula CH6N2. It is used as a rocket propellantinbipropellant rocket engines because it is hypergolic with various oxidizers such as nitrogen tetroxide (N2O4) and nitric acid (HNO3). As a propellant, it is described in specification MIL-PRF-27404.[5]
MMH is a hydrazine derivative that was once used in the orbital maneuvering system (OMS) and reaction control system (RCS) engines of NASA's Space Shuttle, which used MMH and MON-3 (a mixture of nitrogen tetroxide with approximately 3% nitric oxide). This chemical is toxic and carcinogenic,[6] but it is easily stored in orbit, providing moderate performance for very low fuel tank system weight. MMH and its chemical relative unsymmetrical dimethylhydrazine (UDMH) have a key advantage that they are stable enough to be used in regeneratively cooled rocket engines. The European Space Agency (ESA) has attempted to seek new options in terms of bipropellant rocket combinations to avoid using deadly chemicals such as MMH and its relatives.[7]
MMH is believed to be the primary active mycotoxin found in mushrooms of the genus Gyromitra, especially the false morel (Gyromitra esculenta). In these cases, MMH is formed by the hydrolysisofgyromitrin.[8]
Monomethylhydrazine is considered to be a possible occupational carcinogen,[9] and the occupational exposure limits to MMH are set at protective levels to account for the possible carcinogenicity.[10]
A known use of MMH is in the synthesis of suritozole.[11]
MMH is also assumed to be the active methylating agent in the drug Temozolomide.[12]
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Media related to Monomethylhydrazine at Wikimedia Commons
