Triptane
From Wikipedia, the free encyclopedia
Not to be confused with Triplane.
Triptane | |
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IUPAC name 2,2,3-Trimethylbutane[1] | |
Identifiers | |
CAS number | 464-06-2 |
PubChem | 10044 |
ChemSpider | 9649 |
EC number | 207-346-3 |
UN number | 1206 |
Beilstein Reference | 1730756 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C7H16 |
Molar mass | 100.20 g mol−1 |
Appearance | Colorless liquid |
Odor | Odorless |
Density | 693 mg mL−1 |
Melting point | −26 to −24 °C; −15 to −11 °F; 247 to 249 K |
Boiling point | 80.8 to 81.2 °C; 177.3 to 178.1 °F; 353.9 to 354.3 K |
Vapor pressure | 23.2286 kPa (at 37.7 °C) |
kH | 4.1 nmol Pa−1 kg−1 |
Refractive index (nD) | 1.389 |
Thermochemistry | |
Std enthalpy of formation ΔfH |
−238.0 – −235.8 kJ mol−1 |
Std enthalpy of combustion ΔcH |
−4.80449 – −4.80349 MJ mol−1 |
Standard molar entropy S |
292.25 J K−1 mol−1 |
Specific heat capacity, C | 213.51 J K−1 mol−1 |
Hazards | |
GHS pictograms | |
GHS signal word | DANGER |
GHS hazard statements | H225, H304, H315, H336, H400 |
GHS precautionary statements | P210, P261, P273, P301+310, P331 |
EU Index | 601-008-00-2 |
EU classification | F Xn N |
R-phrases | R11, R38, R50/53, R65, R67 |
S-phrases | (S2), S16, S29, S33 |
NFPA 704 |
3
0
0
|
Flash point | −7 °C; 19 °F; 266 K |
Autoignition temperature | 450 °C; 842 °F; 723 K |
Explosive limits | 1–7% |
Related compounds | |
Related alkanes | |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Triptane, or 2,2,3-trimethylbutane, is an organic chemical compound with the molecular formula C7H16 or (H3C-)3C-C(-CH3)2H. It is therefore an alkane, specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C4) backbone.
Triptane is commonly used as an anti-knock additive in aviation fuels.
References
- ↑ "Triptan - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 11 March 2012.
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