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B-naphthyl

AMNES - AMINES,AROMATIC - DIARYLAMINES] (Vol2) N,NQDi-b-naphthyl-p-phenylenediamine [93-46-9]... [Pg.328]

Halide B.P. M.P.. 20° dv 20° "D i Anilide i i a-Naphtha- llde Alkyl Mercuric Halide 1 S-Alkyl- o- thiuronium Pierate Pierate of B-naphthyl ether... [Pg.293]

HaUde B.P. H.P.. 20 20 Anilide a-Naphtha- Ude Alkyl Mercuric Halide S-Alkyl-Ao- thluronium Picrate Picrate o( B-naphthyl ether... [Pg.295]

Procedure A. Ether was added and then the product was washed twice with 3% HCl (15 min. to 1 hr. stir per wash), and then with water until neutral. The ether-insoluble (if any) was collected, washed twice with ether and once with 0.05% Santonox in ether and dried as the ether-insoluble fraction. The ether-soluble was stabilized with 0.5% Santonox (based on total solids), the ether stripped off, and the polymer dried. In Run 7, Table III, the ether-soluble was stabilized with 1% phenyl B-naphthyl amine. [Pg.104]

Unsaturated copolymers were analyzed for the unsaturated comonomer by Kemp Bromine No. (in QKI3) after correcting for the Bromine No, of the antioxidant (Santonox, 125 and phenyl B-naphthyl amine, 143), Chlorine-containing comonomers were determined by a chlorine analysis. The composition of the TMO-EO copolymers was determined by C and H analysis. The PO content of the TMO-PO-AGE terpolymer was determined by infrared analysis. [Pg.105]


See other pages where B-naphthyl is mentioned: [Pg.243]    [Pg.295]    [Pg.228]    [Pg.429]    [Pg.507]    [Pg.515]    [Pg.493]    [Pg.493]    [Pg.495]    [Pg.496]    [Pg.295]    [Pg.2]    [Pg.291]    [Pg.118]    [Pg.264]    [Pg.1544]    [Pg.104]    [Pg.215]    [Pg.229]   
See also in sourсe #XX -- [ Pg.538 ]




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2-Naphthyl

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