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Dinitrophenylhydrazine, purification

Procedures. Chromatographic Purification of Ozonization Products. Ozonization products from ethyl 10-undecenoate and 1-octene were chromatographed on silica gel columns (Baker) and eluted with 15 or 25% ether in petroleum ether (b.p., 30°-60°). Fractions were examined by thin-layer chromatography (TLC) on silica gel G Chroma-gram sheet eluted with 40% ether in petroleum ether. For development of ozonide and peroxide spots, 3% KI in 1% aqueous acetic acid spray was better than iodine. The spots (of iodine) faded, but a permanent record was made by Xerox copying. Color of die spots varied from light brown (ozonide) to purple-brown (hydroperoxide), and the rate of development of this color was related to structure (diperoxide > hydroperoxide > ozonide). 2,4-Dinitrophenylhydrazine spray revealed aldehyde spots and also reacted with ozonides and hydroperoxides. Fractions were evaporated at room temperature or below in a rotary evaporator. [Pg.258]


See other pages where Dinitrophenylhydrazine, purification is mentioned: [Pg.119]    [Pg.157]    [Pg.163]    [Pg.254]    [Pg.274]    [Pg.284]    [Pg.136]    [Pg.143]    [Pg.231]    [Pg.250]    [Pg.260]    [Pg.99]    [Pg.136]    [Pg.143]    [Pg.250]    [Pg.260]    [Pg.119]    [Pg.157]    [Pg.163]    [Pg.254]    [Pg.274]    [Pg.284]    [Pg.83]    [Pg.113]    [Pg.147]    [Pg.155]    [Pg.130]    [Pg.176]    [Pg.181]    [Pg.95]    [Pg.130]    [Pg.176]    [Pg.272]   
See also in sourсe #XX -- [ Pg.217 ]




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2,4"Dinitrophenylhydrazine

Dinitrophenylhydrazin

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