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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 is an organic chemical widely used as stabilising additive (or antidegradant) in rubbers, such as NR, SBR and BR; all of which are common in vehicle tires. [1] Although it is an effective antioxidant it is primarily used because of its excellent antiozonant performance.

  4. Diamine - Wikipedia

    en.wikipedia.org/wiki/Diamine

    A diamine is an amine with exactly two amino groups.Diamines are used as monomers to prepare polyamides, polyimides, and polyureas.The term diamine refers mostly to primary diamines, as those are the most reactive.

  5. 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]

  6. 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 ...

  7. Spot test (lichen) - Wikipedia

    en.wikipedia.org/wiki/Spot_test_(lichen)

    The phenylenediamine reacts with aldehydes to yield Schiff bases according to the following reaction: [9] R−CHO + H 2 N−C 6 H 4 −NH 2 → R−CH=N−C 6 H 4 −NH 2 + H 2 O. Products of this reaction are yellow to red in colour. Most β-orcinol depsidones and some β-orcinol depsides will react positively. [11]

  8. 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.

  9. 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.