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Amines, tert dimethylamines

It was suggested that the dimethylamine would react with epoxide and that the resulting tert-amine would catalyse epoxide homopolymerisation. LaLiberte et al. 63) found that Monuron or Diuron could react with epoxide to form an oxazolidone and dimethylamine ... [Pg.125]

An azophenol crown including a pyridine unit, 66, (Fig. 19) reacts with all of amines in acetonitrile to form ammonium phenolates. The absorption maxima of 66-prim, amine systems appear in a region of 574-586 nm, which is definitely distinct from those of sec. and tert. amine systems (Xmax 602 — 606 nm except for the dimethylamine system which gave 592 nm) as shown in Fig. 19. On the other hand, a dyed crown including an additional benzene unit, 65 (Fig. 19), reacts with various amines to make ammonium phenolates which show absorption maxima of nearly constant wavelength. [Pg.190]

Synonyms Alkyl (C13-15) dimethylamine C13-15 dimethyl tert. amine Dimethylalkyl (C13-C15) amine... [Pg.1408]


See other pages where Amines, tert dimethylamines is mentioned: [Pg.233]    [Pg.52]    [Pg.292]    [Pg.176]    [Pg.330]    [Pg.382]    [Pg.6758]    [Pg.242]   


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Tert-Amines

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