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Dimethyl-p-phenylene diamine

The azastyryl dyes result from the condensation of 2-formylthiazolium salt either on N,N-dimethyl-p-phenylene diamine or aromatic nitroso derivative. [Pg.241]

When p-ethylaminobenzoate and N,N-dimethyl-p-phenylene diamine sulfate were similarly treated with the dibromosulfone (I) for 2 h, the yield was only 32% and 15% respectively (Figure 1). A possible explanation is that the nucleophilicity of these monosubstituted anilines is weaker than that of aniline while a Na2C03 1,4-HBr elimination reaction could be competing with the substitution reaction, leading to the lower yield (18). [Pg.128]

Sediment Trap hydrogen sulfide in sodium hydroxide sulfide reacts with AW-dimethyl-p-phenylene-diamine to from methylene blue. Colorimetry 0.01 pmol/gram NR Allen et al. 1994... [Pg.162]

Preparation of Bindschedler s Green.1—Dimethyl-p-phenylene-diamine (7 g.) and dimethylaniline (6 g.) are dissolved in a mixture of 40 c.c. of concentrated hydrochloric acid and 40 c.c. of water. Into the solution, which is kept cool in ice and is stirred mechanically or... [Pg.321]

Chloride, (H3C)2N.CGH4.N( N).Cl, mw 183.64, N 22.88% pale-yel crysts (from ale + eth), mp — puffs off at ca 130° sol in cold w in ale insol in eth decumpd by hot w. Hantzsch (Refs 1 2) prepd it hy the low-temp diazotization of N -dinethyl-p-phenyl-enediamine with Na nitrite, while Stolle (Ref 4) treated N,N-dimethyl-p-phenylene-diamine hydrochloride with amyl nitrite in alcoholic medium... [Pg.212]

In Fig. 12 (curves 1 and 2) the double peaked absorption maximum, 520 and 560 m a is shown, characteristic of the positive ion-radical of dimethyl-p-phenylene diamine (MejN—Ph—NHa)t (77), which was here obtained by adsorption of the vapor under high vacuum conditions (27, 78). The same interpretation is given to the absorption maximum 850 m/a for benzidine vapor, adsorbed on silica-alumina gel (curves 3 and 4), which does not appear on silica gel. The band of the benzidine ion-radical, obtained by photoionization in the rigid EPA solvent at - 180°C is situated at 885 m/x (76). The accompanying bands 760 and 450 seem to be intimately connected with that at 850 m/a. [Pg.257]

On the catalytically active silica-alumina oxygen, or air, reacts with the adsorbed cation radicals, e.g., those of iV-dimethyl-p-phenylene-diamine, already on staying at room temperature (48a). Irreversible oxygenated products and a presumed diamine-Oj complex are formed. [Pg.274]

Thus, p-dimethylaminoazobenzene yields aniline and dimethyl-p-phenylene-diamine on reduction —... [Pg.471]

Figure 8A. Stoichiometry of the reaction of III with dimethyl-p-phenylenediamine. Experiments carried out strictly at 0°C. to avoid decomposition of III. Milh-molar extinction coefficient of dimethyl-p-phenylene-diamine radical was 8.7 at 515 nifi... Figure 8A. Stoichiometry of the reaction of III with dimethyl-p-phenylenediamine. Experiments carried out strictly at 0°C. to avoid decomposition of III. Milh-molar extinction coefficient of dimethyl-p-phenylene-diamine radical was 8.7 at 515 nifi...
The earliest tests used for this purpose were made with the Nadi reagent. This reagent consists of a mixture of a-naphthol and dimethyl-p-phenylene-diamine, which under the influence of certain oxidases is converted into a blue indophenol derivative. [Pg.395]


See other pages where Dimethyl-p-phenylene diamine is mentioned: [Pg.1630]    [Pg.324]    [Pg.173]    [Pg.150]    [Pg.232]    [Pg.291]    [Pg.259]    [Pg.230]    [Pg.1630]    [Pg.304]    [Pg.1630]    [Pg.41]    [Pg.119]    [Pg.387]   
See also in sourсe #XX -- [ Pg.313 ]




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