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Benzenediazonium tetrachlorozincate

Benzenediazonium-4-sulfonate, 2193 Benzenediazonium tetrachlorozincate, 3476 Benzenediazonium tribromide, 2227... [Pg.116]

The dry salt was more or less explosive, depending on the method of preparation [1]. DTA examination of a 15% solution of the diazonium salt in hydrochloric acid showed an exothermic decomposition reaction with the exotherm peak at 65°C. Adiabatic decompositon of the solution at 20°C took 80 min to attain the maximum temperature of 80°C [2]. The heat of decomposition Q was determined as 1.5 kJ/g [3], See Benzenediazonium tetrachlorozincate... [Pg.806]

Benzenediazonium-2-carboxylate, 2655 Benzenediazonium-3-carboxylate, 2656 Benzenediazonium-4-carboxylate, 2657 Benzenediazonium chloride, 2223 Benzenediazonium hydrogen sulfate, 2311 Benzenediazonium iodide, 2243 Benzenediazonium nitrate, 2268 Benzenediazonium-4-oxide, 2182 Benzenediazonium perchlorate, 2225 Benzenediazonium-2-sulfonate, 2185 Benzenediazonium-4-sulfonate, 2186 Benzenediazonium tetrachlorozincate, 3469 Benzenediazonium tetrafluoroborate, 2216 Benzenediazonium tetraphenylborate, 3870a Benzenediazonium tribromide, 2220 Benzenediazonium triiodide, 2247... [Pg.2049]

Amino-3-phenyl-1,2,4-triazole, Nitrous acid, 2947 Benzenediazonium chloride, 2223 Benzenediazonium iodide, 2243 Benzenediazonium nitrate, 2268 Benzenediazonium tetrachlorozincate, 3469 Benzenediazonium tribromide, 2220... [Pg.2302]

See other pages where Benzenediazonium tetrachlorozincate is mentioned: [Pg.728]    [Pg.1147]    [Pg.1208]    [Pg.1199]    [Pg.1256]    [Pg.728]    [Pg.1147]    [Pg.1208]    [Pg.728]    [Pg.1208]    [Pg.1960]    [Pg.728]    [Pg.1147]    [Pg.1208]    [Pg.1199]    [Pg.1256]    [Pg.728]    [Pg.1147]    [Pg.1208]    [Pg.728]    [Pg.1208]    [Pg.1960]    [Pg.68]    [Pg.115]    [Pg.96]    [Pg.2302]    [Pg.2219]   


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