Neopentane
|  | |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name 2,2-Dimethylpropane | |||
| Other names Neopentane Tetramethylmethane | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| 1730722 | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.006.677 | ||
| EC Number | 
 | ||
| 1850 | |||
| MeSH | neopentane | ||
| PubChem CID | |||
| UNII | |||
| UN number | 2044 | ||
| CompTox Dashboard (EPA) | |||
| 
 | |||
| 
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| Properties | |||
| C5H12 | |||
| Molar mass | 72.151 g·mol−1 | ||
| Appearance | Colorless gas | ||
| Odor | Odorless | ||
| Density | 3.255 kg/m3 (gas, 9.5 °C) 601.172 kg/m3 (liquid, 9.5 °C) | ||
| Melting point | −16.5 °C (2.3 °F; 256.6 K) | ||
| Boiling point | 9.5 °C (49.1 °F; 282.6 K) | ||
| Vapor pressure | 146 kPa (at 20 °C) | ||
| Henry's law constant (kH) | 4.7 nmol Pa−1 kg−1 | ||
| Thermochemistry | |||
| Heat capacity (C) | 121.07–120.57 J K−1 mol−1 | ||
| Std molar entropy (S⦵298) | 217 J K−1 mol−1 | ||
| Std enthalpy of formation (ΔfH⦵298) | −168.5–−167.3 kJ mol−1 | ||
| Std enthalpy of combustion (ΔcH⦵298) | −3.51506–−3.51314 MJ mol−1 | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H220, H411 | |||
| P210, P273, P377, P381, P391, P403, P501 | |||
| NFPA 704 (fire diamond) | |||
| Related compounds | |||
| Related alkanes | |||
| Related compounds | |||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Neopentane, also called 2,2-dimethylpropane, is a double-branched-chain alkane with five carbon atoms. Neopentane is a flammable gas at room temperature and pressure which can condense into a highly volatile liquid on a cold day, in an ice bath, or when compressed to a higher pressure.
Neopentane is the simplest alkane with a quaternary carbon, and has achiral tetrahedral symmetry. It is one of the three structural isomers with the molecular formula C5H12 (pentanes), the other two being n-pentane and isopentane. Out of these three, it is the only one to be a gas at standard conditions; the others are liquids.
It was first synthesized by Russian chemist Mikhail Lvov in 1870.