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  2. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    p-Xylene (para-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes . The p- stands for para- , indicating that the two methyl groups in p -xylene occupy the diametrically opposite substituent positions 1 and 4.

  3. p-Xylene (data page) - Wikipedia

    en.wikipedia.org/wiki/P-Xylene_(data_page)

    for p-Xylene/carbon tetrachloride [6] P = 760 mm Hg BP Temp. °C % by mole carbon tetrachloride liquid ... Spectrum NIST: Major absorption bands 793.94 cm −1: NMR;

  4. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    p-Xylene is the principal precursor to terephthalic acid and dimethyl terephthalate, both monomers used in the production of polyethylene terephthalate (PET) plastic bottles and polyester clothing. 98% of p-xylene production, and half of all xylenes produced is consumed in this manner. [10] [14] o-Xylene is an important precursor to phthalic ...

  5. Aniline (data page) - Wikipedia

    en.wikipedia.org/wiki/Aniline_(data_page)

    m-xylene (data page) p-xylene (data page) Vapor-liquid Equilibrium for Aniline/Water [6] P = 745 mm Hg BP Temp. °C % by mole water liquid vapor 98.5: 96.5 101: 24.7: ...

  6. o-Xylene - Wikipedia

    en.wikipedia.org/wiki/O-Xylene

    o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C 6 H 4 (CH 3) 2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). It is a constitutional isomer of m -xylene and p -xylene , the mixture being called xylene or xylenes.

  7. Parylene - Wikipedia

    en.wikipedia.org/wiki/Parylene

    α,α'-dimethoxy-p-xylene. A similar synthesis for parylene N uses the precursor α,α'-dimethoxy-p-xylene. [28] The methoxy group H 3 CO − is the leaving group; while it condenses in the deposition chamber, it does not interfere with the deposition of the polymer. [23] This precursor is much less expensive than [2.2]para-cyclophane.

  8. Terephthalic acid - Wikipedia

    en.wikipedia.org/wiki/Terephthalic_acid

    Terephthalic acid was produced by oxidation of p-xylene with 30-40% nitric acid. Air oxidation of p-xylene gives p-toluic acid, which resists further air-oxidation. Esterification of p-toluic acid to methyl p-toluate (CH 3 C 6 H 4 CO 2 CH 3) opens the way for further oxidation to monomethyl terephthalate. In the Dynamit−Nobel process these ...

  9. 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.