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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]
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 ...
2-Propenoic acid, polymer with 2 p-propenamide, sodium salt / copolymer of acrylamide and sodium acrylate: Friction reducer 71050-62-9: 2-Propenoic acid, polymer with sodium phosphinate (1:1) No record 66019-18-9: 2-propenoic acid, telomer with sodium hydrogen sulfite: No record 107-19-7: 2-Propyn-1-ol / propargyl alcohol: No record 51229-78-8
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 ...
The Pinnick oxidation is an organic reaction by which aldehydes can be oxidized into their corresponding carboxylic acids using sodium chlorite (NaClO 2) under mild acidic conditions. It was originally developed by Lindgren and Nilsson. [ 1 ]
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 ]
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.
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 ]