| Hexane | |
|---|---|
| General | |
| Other names | n-Hexane |
| Molecular formula | C6H14 |
| SMILES | CCCCCC |
| Molar mass | 86.18 g/mol |
| Appearance | colorless liquid |
| CAS number | * |
| Properties | |
| Density and phase | 0.6548 g/ml, liquid |
| Solubility in water | immiscible |
| Melting point | −95 °C (178 K) |
| Boiling point | 69 °C (342 K) |
| Viscosity | 0.294 cP at 25 °C |
| Hazards | |
| MSDS | External MSDS |
| EU classification | Flammable (F) Harmful (Xn) Repr. Cat. 3 Dangerous for the environment (N) |
| NFPA 704 | |
| R-phrases | , , , , , , |
| S-phrases | , , , , , , , |
| Flash point | −23.3 °C |
| Autoignition temperature | 233.9 °C |
| Explosive limits | 1.2–7.7% |
| RTECS number | MN9275000 |
| Supplementary data page | |
| Structure and properties | n, εr, etc. |
| Thermodynamic data | Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Related compounds | |
| Related alkanes | Pentane Hexanes Heptane |
| Related compounds | Cyclohexane |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Chemical infobox | |
Hexane is an alkane hydrocarbon with the chemical formula CH3(CH2)4CH3. The "hex" prefix refers to its six carbons, while the "ane" ending indicates that its carbons are connected by single bonds. Hexane isomers are largely unreactive, and are frequently used as an inert solvent in organic reactions because they are very non-polar. They are also common constituents of gasoline. Hexane has five isomers:
Chronic intoxication from hexane has been observed in recreational solvent abusers and in workers in the shoe manufacture, furniture restoration and automobile construction. The initial symptoms are tingling and cramps in the arms and legs, followed by general muscular weakness. In severe cases, atrophy of the skeletal muscles is observed, along with a loss of coordination and problems of vision.
Similar symptoms are observed in animal models. They are associated with a degeneration of the peripheral nervous system (and eventually the central nervous system), starting with the distal portions of the longer and wider nerve axons. The toxicity is not due to hexane itself but to one of its metabolites, hexane-2,5-dione. It is believed that this reacts with the amino group of the side chain of lysine residues in proteins, causing cross-linking and a loss of protein function.
The effects of hexane poisoning in humans are not permanent, and usually disappear gradually over one to three years after the end of exposure.
هيكسان | Hexan | Hexano | Heksano | Hexane | Hexaan | ヘキサン | Heksan | Hexano | Хексан | Heksaani | Hexan