3-Methylpentane is a branched alkane with the molecular formula C6H14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain. It is of similar structure to the isomeric 2-methylpentane, which has the methyl group located on the second carbon of the pentane chain.
| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
3-Methylpentane[1] | |||
Identifiers | |||
3D model (JSmol) |
|||
1730734 | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.002.257 | ||
EC Number |
| ||
MeSH | 3-methylpentane | ||
PubChem CID |
|||
RTECS number |
| ||
UNII | |||
UN number | 1208 | ||
CompTox Dashboard (EPA) |
|||
| |||
| |||
Properties | |||
C6H14 | |||
Molar mass | 86.178 g·mol−1 | ||
Appearance | Colorless liquid | ||
Odor | Odorless | ||
Density | 664 mg mL−1 | ||
Melting point | −162.8 °C; −261.1 °F; 110.3 K | ||
Boiling point | 62.9 to 63.7 °C; 145.1 to 146.6 °F; 336.0 to 336.8 K | ||
Insoluble | |||
log P | 3.608 | ||
Vapor pressure | 18.0 kPa (at 17 °C) | ||
Henry's law constant (kH) |
8.8 mol Pa−1 kg−1 | ||
-75.52·10−6 cm3/mol | |||
Refractive index (nD) |
1.376 | ||
Thermochemistry | |||
Heat capacity (C) |
191.16 J K−1 mol−1 | ||
Std molar entropy (S⦵298) |
292.5 J K−1 mol−1 | ||
Std enthalpy of formation (ΔfH⦵298) |
−203.0–−201.0 kJ mol−1 | ||
Std enthalpy of combustion (ΔcH⦵298) |
−4.1608–−4.1590 MJ mol−1 | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H225, H304, H315, H336, H411 | |||
P210, P261, P273, P301+P310, P331 | |||
Flash point | −7 °C (19 °F; 266 K) | ||
278 °C (532 °F; 551 K) | |||
Explosive limits | 1.2–7.7% | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible) |
none[2] | ||
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).
|
It is formed by (Pentan-2-ol)+(3-methyl)=3-methylpentan-2-ol
References
External links
Wikiwand in your browser!
Seamless Wikipedia browsing. On steroids.
Every time you click a link to Wikipedia, Wiktionary or Wikiquote in your browser's search results, it will show the modern Wikiwand interface.
Wikiwand extension is a five stars, simple, with minimum permission required to keep your browsing private, safe and transparent.