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Triptane, or 2,2,3-trimethylbutane, is an organic chemical compound with the molecular formula C 7 H 16 or (H 3 C-) 3 C-C(-CH 3) 2 H. It is therefore an alkane , specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C 4 ) backbone.
2,3,3-Trimethylpentane is a chemical compound in the family of hydrocarbons which has a formula of C 8 H 18. It is an isomer of octane . It has a role as a human metabolite, a bacterial metabolite and a mammalian metabolite. [ 2 ]
2,3,4-Trimethylpentane Tetra- tert -butylmethane Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Tetramethylbutane, sometimes called hexamethylethane, is a hydrocarbon with formula C 8 H 18 or (H 3 C-) 3 C-C(-CH 3) 3. It is the most heavily branched and most compact of the octane isomers, the only one with a butane (C4) backbone. Because of its highly symmetrical structure, it has a very high melting point and a short liquid range; in fact ...
Often it requires a strong working knowledge of a language to evaluate and understand redirects – for example, being able to identify that a Chinese redirect is using the wrong character, or a Romanian redirect has an incorrect diacritical mark that looks almost identical to the correct one. [2]
The speed of sound at 3 MHz is 1149.5 m/s at 20 °C and 889.5 m/s at 80 °C. [ 7 ] [ 8 ] [ 9 ] The racemic mixture has a glass transition temperature of about 123 K (−150 °C), but reportedly it does not crystallize—a fact that has been claimed to be a characteristic of high-purity optically active alkanes.
2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.
(C 6 H 5) 3 CCl + 2 Na → (C 6 H 5) 3 CNa + NaCl. The use of tritylsodium as a strong, non-nucleophilic base has been eclipsed by the popularization of butyllithium and related strong bases. The unmodified anion is red, and can be used as an indicator in acid–base titrations. Derived substances have proven useful as chemical dyes.