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  2. p-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/P-Phenylenediamine

    p-Phenylenediamine (PPD) is an organic compound with the formula C 6 H 4 (NH 2) 2. This derivative of aniline is a white solid, but samples can darken due to air oxidation. [1] It is mainly used as a component of engineering polymers and composites like kevlar. It is also an ingredient in hair dyes and is occasionally used as a substitute for ...

  3. 6PPD - Wikipedia

    en.wikipedia.org/wiki/6PPD

    6PPD itself is deadly to rotifers, especially in combination with sodium chloride, though not at the level generally found in the runoff from road salt. [21] A small-scale biomonitoring study in South China has shown both 6PPD and 6PPDQ to be present in human urine; concentrations were low but the health implications are unknown. [ 22 ]

  4. Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/Phenylenediamine

    Phenylenediamine may refer to: o-phenylenediamine or OPD, a chemical compound C 6 H 4 (NH 2) 2; m-phenylenediamine or MPD, a chemical compound C 6 H 4 (NH 2) 2; p-phenylenediamine or PPD, a chemical compound C 6 H 4 (NH 2) 2; N,N-dimethyl-p-phenylenediamine or DMPD; N,N,N′,N′-tetramethyl-p-phenylenediamine or TMPD, used in microbiology; N,N ...

  5. 4-Aminodiphenylamine - Wikipedia

    en.wikipedia.org/wiki/4-Aminodiphenylamine

    An alternative is the direct reaction of nitrobenzene with aniline via a nucleophilic aromatic substitution of hydrogen (vicarious nucleophilic substitution). [ 5 ] [ 6 ] This again requires a reduction step but is a good example of industrial green chemistry as it eliminates the need for organochlorine starting materials and metal catalysts.

  6. m-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/M-Phenylenediamine

    m-Phenylenediamine, also called 1,3-diaminobenzene, is an organic compound with the formula C 6 H 4 (NH 2) 2. It is an isomer of o -phenylenediamine and p -phenylenediamine . This aromatic diamine is a colourless solid that appears as needles, but turns red or purple on exposure to air due to formation of oxidation products. [ 3 ]

  7. Wurster's blue - Wikipedia

    en.wikipedia.org/wiki/Wurster's_blue

    Wurster's blue is the radical cation of the colorless chemical N,N,N′,N′-tetramethyl-p-phenylenediamine, also known as TMPD. [1] This is an easily oxidized phenylenediamine, which loses two electrons in one-electron oxidation steps; the radical cation is a characteristic blue-violet color, which gives the compound part of its name.

  8. o-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/O-Phenylenediamine

    o-Phenylenediamine (OPD) is an organic compound with the formula C 6 H 4 (NH 2) 2. This aromatic diamine is an important precursor to many heterocyclic compounds. OPD is a white compound although samples appear darker owing to oxidation by air. It is isomeric with m-phenylenediamine and p-phenylenediamine.

  9. N-Isopropyl-N'-phenyl-1,4-phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-Isopropyl-N'-phenyl-1,4...

    N-Isopropyl-N′-phenyl-1,4-phenylenediamine (often abbreviated IPPD) is an organic compound commonly used as an antiozonant in rubbers. [1] Like other p-phenylenediamine -based antiozonants it works by virtue of its low ionization energy , which allows it to react with ozone faster than ozone will react with rubber. [ 2 ]

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