Benzene hydrocarbons

Nitrol. Early Brit plastic safety expl, patented by O. Silberrad in 1912 (Ref 2). A typical formulation is Nitrol 10, highly. nitrated benzene hydrocarbons 20, collodion cotton 0.5, and AN 69.5%. Under the same name, O. Silberrad took... 

Using other alkylated benzene hydrocarbons, e.g., amyl-, hexyl-, octyl-, or nonylbenzene, similar surface-active phosphinic acids are formed by reaction with PC13 in the presence of anhydrous aluminum trichloride. The resulting alkylarylphosphinic acids form stable salts with primary, secondary, or tertiary hydroxy amines or aromatic amines [166,171]. 

Kulprathipanja, S., Kuhnle, K., Patton, M.S., and Fergin, R.L. (1993) Process for separabng naphthalene from subsbtuted benzene hydrocarbons. U.S. Patent 5,177,300. 

Sanemasa, I., Miyazaki, Y., Arakawa. S.. Kumamaru, M.. and Deguchi. T. The solubility of benzene-hydrocarbon binary mixtures in water, Bull Chem. Soc. Jpn., 60(2) 517-523, 1987. 

Most effort over the electrochemical reduction of benzene hydrocarbons has centred on finding a reaction medium, which is also a better solvent for the substrate than liquid ammonia. Aliphatic amines have proved useful solvents and they may be used in an undivided electrochemical cell. Base is generated at the cathode while an equivalent of acid is generated in the anode reaction so that mixing of the cel contents maintains a neutral solution. An alcohol is usually added as a proton donor to prevent the build-up of a localised highly basic environment. The simultaneous anode reaction is oxidation of the amine. Electrodes of platinum, aluminium or graphite have been used. Under these conditions, benzene [38] is converted... 

Benzene hydrocarbons are known to undergo radical coupling reactions and the intramolecular reductive coupling of carbonyl compounds with a benzene ring has been achieved. Best conditions for this process are at a tin cathode with isopropanol solvent and tetaethylammonium tosylate as supporting electrolyte [102, 103], The reaction is performed at constant current in a divided cell. A single stereoiso-... 

Trichlorophenoxyacetic, 2,4,5 Acid Dioxin and Related Compounds Dioxin and Related Compounds HxCDF Hexachlorodibenzofurans TCDD Tetrachlorodibenzodioxins TCDF Tetrachlorodibenzofurans Disubstituted and Polysubstituted Benzene Hydrocarbons Diethyl Benzene... 

Benzene under Benzene and Monosubstituted Benzene Hydrocarbons Benzene and Monosubstituted Benzene Hydrocarbons Benzene and Substituted Benzene Hydrocarbons Benzene, Toluene, Ethylbenzene, and Xylene (BTEX)... 

Biphenyl under Benzene and Monosubstituted Benzene Hydrocarbons Bismuth... 

Diethyl Benzene under Disubstituted and Polysubstituted Benzene Hydrocarbons Diethyl Ether under Noncyclic Aliphatic or Aromatic Ethers Dihalogenated and Polyhalogenated Ethers... 

Ethylbenzene under Benzene and Monosubstituted Benzene Hydrocarbons Ethyl Chloride Chloroethane under Saturated Alkyl Halides Ethyl Lactate Hydroxypropanoic Acid, Ethyl Ester under Esters Ethylene under Alkenes, Cyclic Alkenes, and Dienes... 

Indene Dihydroindene under Disubstituted and Polysubstituted Benzene Hydrocarbons Indene under Polycyclic Hydrocarbons, Nonaltemant Compounds with Two or Three Fused Rings Indeno(l,2,3-C(i0pyrene under Poiycyciic Hydrocarbons, Nonaltemant Compounds with More Than Five Fused Rings Iodine Iron... 

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