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  2. tert-Amyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_chloride

    tert-Amyl chloride (2-methyl-2-butyl chloride) is an alkyl chloride used for flavoring and odorizing. [2] At room temperature, it is a colorless liquid with an unpleasant odor. It is an isomer of 1-chloropentane ( n -amyl chloride).

  3. Amyl chloride - Wikipedia

    en.wikipedia.org/wiki/Amyl_chloride

    Amyl chloride may refer to any of the monochlorinated derivatives of the isomers of pentane. They have the molecular formula C 5 H 11 Cl. tert-Amyl chloride; 1-Chloropentane (n-amyl chloride) 2-Chloropentane; 3-Chloropentane; 1-Chloro-3-methylbutane (isoamyl chloride)

  4. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Toggle the table of contents. List of boiling and freezing information of solvents. ... tert-Butanol: 82.5 [14] Chlorobenzene: 131.7 [15] p-chlorobenzotrifluoride: 1.34

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. 1-Chloropentane - Wikipedia

    en.wikipedia.org/wiki/1-Chloropentane

    Toggle the table of contents. ... n-Pentyl chloride; n-Amyl chloride. Identifiers CAS Number. 543-59-9 ... tert-Amyl chloride; References

  7. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

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  9. 3,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/3,3-Dimethylpentane

    A method to produce 3,3-dimethylpentane is to react tert-amyl chloride (CH 3 CH 2 (CH 3)C 2 Cl) with propionaldehyde producing 3,3-dimethylpentan-2-ol. This is then dehydrated to produce 3,3-dimethylpent-2-ene, which when hydrogenated produces some 3,3-dimethylpentane, but also 2,3-dimethylpentane. [2]