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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. 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.

  5. List of metal-organic chemical vapour deposition precursors

    en.wikipedia.org/wiki/List_of_metal-organic...

    "• 30 g/L at 20 °C Medium: tert-butyl alcohol • 70 g/L at 20 °C Medium: Toluene • 130 g/L at 20 °C Medium: Hexane • 380 g/L at 20 °C Medium: Tetrahydrofuran • 50 g/L at 20 °C Medium: xylene • 110 g/L at 20 °C Medium: octane • 220 g/L at 20 °C Medium: Diethyl ether • 450 g/L at 20 °C Medium: Dimethylformamide

  6. 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]

  7. Tammann and Hüttig temperatures - Wikipedia

    en.wikipedia.org/wiki/Tammann_and_Hüttig...

    The Tammann temperature (also spelled Tamman temperature) and the Hüttig temperature of a given solid material are approximations to the absolute temperatures at which atoms in a bulk crystal lattice (Tammann) or on the surface (Hüttig) of the solid material become sufficiently mobile to diffuse readily, and are consequently more chemically reactive and susceptible to recrystallization ...

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  9. Pentyl group - Wikipedia

    en.wikipedia.org/wiki/Pentyl_group

    The nomenclature has now reversed, with "amyl" being more often used to refer to the terminally branched group also called isopentyl, as in amobarbital. A cyclopentyl group is a ring with the formula -C 5 H 9. The name is also used for the pentyl radical, a pentyl group as an isolated molecule. This free radical is only observed in extreme ...