Triptane

It is therefore an alkane, specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C4) backbone.

It was first synthesized in 1922 by Belgian chemists Georges Chavanne (1875–1941) and B. Lejeune, who called it trimethylisopropylmethane.

[2][3] Due to its high octane rating (112–113 RON, 101 MON[4][5]) triptane was produced on alkylation units starting from 1943[6] for use as an anti-knock additive in gasoline.

It was extensively researched for this role and received the modern name in the late 1930s at a joint laboratory of NACA, National Bureau of Standards, US Army Air Corps and the Bureau of Aeronautics.

[7] As of 2011, it was not a significant component of US automobile gasoline, present only in trace amounts (0.05–0.1%).

Skeletal formula of triptane
Skeletal formula of triptane
Ball-and-Stick model of triptane
Ball-and-Stick model of triptane
NFPA 704 four-colored diamond Health 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chloride Flammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasoline Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code