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  2. Heptane - Wikipedia

    en.wikipedia.org/wiki/Heptane

    Heptane or n-heptane is the straight-chain alkane with the chemical formula H 3 C(CH 2) 5 CH 3 or C 7 H 16. When used as a test fuel component in anti-knock test engines, a 100% heptane fuel is the zero point of the octane rating scale (the 100 point is 100% iso-octane ).

  3. 2-Methylheptane - Wikipedia

    en.wikipedia.org/wiki/2-Methylheptane

    It is an heptane molecule with a methyl group attached to its second atom. It is a flammable colorless liquid used as fuel. [2] If the standard definition of the prefix "iso-" is strictly used then 2-methylheptane can be called "Isooctane". However this name is usually used for another much more important isomer of octane 2,2,4-trimethylpentane ...

  4. 3-Methylheptane - Wikipedia

    en.wikipedia.org/wiki/3-Methylheptane

    Its structural formula is CH 3 CH 2 CH(CH 3)CH 2 CH 2 CH 2 CH 3. It has one stereocenter. Its refractive index is 1.398 (20 °C, D). [citation needed] References

  5. 2-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/2-Methylhexane

    Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of liquid is found in 2-Methylhexane than heptane. On the NFPA 704 scale, 2-methylhexane is listed as a reactivity level-0 chemical, along with various other alkanes.

  6. 3-Ethylpentane - Wikipedia

    en.wikipedia.org/wiki/3-ethylpentane

    It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol .

  7. 3-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/3-Methylhexane

    3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane.. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane.

  8. Heptanal - Wikipedia

    en.wikipedia.org/wiki/Heptanal

    The formation of heptanal in the fractional distillation of castor oil [3] was already described in 1878. The large-scale production is based on the pyrolytic cleavage of ricinoleic acid [4] (Arkema method) and on the hydroformylation of 1-hexene with rhodium 2-ethylhexanoate as a catalyst upon addition of some 2-ethylhexanoic acid (Oxea method): [2] [5]

  9. 3-Heptanone - Wikipedia

    en.wikipedia.org/wiki/3-Heptanone

    3-Heptanone (butyl ethyl ketone), is a seven carbon ketone.It is a colorless liquid with a "green odor," also described to have a fruity scent. It is often used as a perfume/fragrance, as a solvent for cellulose, nitrocellulose, or vinyl resins, and as a synthetic building block in the preparation of other organic molecules.