Ethylamine Ethylene

Cyclohexanol, Cyclopentane, Cyclopentene, 1,2-Dichloroethane, Diethyl phthalate, 1,4-Dioxane, Ethephon. Ethylamine, Ethylene dibromide, Ethylenimine, p-Propiolactone, Tetraethyl pyrophosphate, TCDD, 1,1,1-Trichloroethane, Trichloroethylene, Vinyl chloride Ethylene chlorohydrin, see Bis(2-chloroethyl) ether Ethylenediamine, see Ethylene thiourea. Maneb Ethylene glycol, see Bis(2-chloroethyl) ether, 1,2-Dichloroethane, Ethylene chlorohydrin. Ethylene dibromide... [Pg.1529]

Monoethanolamine Ethylamine Ethylene Glycol Vinyl Fluoride Ethylene Glycol Calcium Phosphate Isobutylamine Monoisopropanolamine Isopropylamine Methylamne Methylcrazine Nitric Oxide Pentaerythritol... [Pg.68]

AI04 4P04(=0) ethylamine ethylene glycol, s-butyl alcohol... [Pg.149]

Ethyl Cyanoacetate Ethylamine Ethylene Bromide Ethylene Chloride... [Pg.472]

Diphenamid Dodine Endosulfan Ethylamine Ethylene dichloride... [Pg.5514]

Lithium ethylamine Ethylene derivs. from alkoxy-2-ethylenes... [Pg.29]

Lithium ethylamine Ethylene derivatives from dienes... [Pg.38]

Ethox ML-5 Ethox ML-9 Ethox ML-14 Ethox MO-9 Ethox MO-14 Ethox MS-8 Ethox MS-14 Ethox MS-23 Ethox MS-40 Ethox TO-8 Ethox TO-9A Ethox TO-16 Ethylacrylate/methylacryllc acid copolymer Ethylamine Ethylene Ethylene glycol diethyl ether Ethylene/MA copolymer 2-Ethylhexylamlne Ethyl-hexyl dipropionate Ethyl hydroxymethyl oleyl oxazoline Etocas 35 Eureka 102 EuroNao AMF Ultra ... [Pg.2577]

A number of 2eohtic materials have been claimed to cataly2e this reaction and reaction temperatures are on the order of 200—350°C with pressures as high as 18000 kPa (2600 psi) reported. This is a low conversion process and recycle of the unconverted starting materials is necessary to provide an economical process. Amination of ethylene to produce ethylamines cataly2ed by ammonium iodide is reported, but not beheved to be practiced commercially (15,16). Alkyl Halide Amination (Method 7). The oldest technology for pioducing amines is the reaction of ammonia with an alkyl hahde. This... [Pg.200]

Ethoheptazine as analgesic, 1, 167 Ethosuximide as anticonvulsant, 1, 166 Ethoxzolamide as diuretic, 1, 173 Ethylamine, o-bromophenyl-indole synthesis from, 4, 322 Ethylamine, 2-thienyl-biological activity, 4, 911 Ethylamine, 3-thienyl-biological activity, 4, 912 Ethylene... [Pg.623]

In a typical case, ethylamine is allowed to react with ethylene oxide to produce N-ethyldiethanolamine (5). The latter is then treated with additional ethylene oxide to afford N,N-di(polyoxyethylene)ethylamine (6) where the sum a -t b is 3. This material is then stirred at room temperature for 3 h with toluenesulfonyl chloride and powdered sodium hydroxide in dioxane solution. After filtration and Kugelrohr distillation, N-eth-ylmonoaza-15-crown-5 is isolated in 75% yield as illustrated below in Eq. (4.7). [Pg.158]

A mixture of 142.5 g of "Rosin Amine D" containing about 70% dehydroabietylamine and 30% dihydro and tetrahydroabietylamine, 47.0 g of ethylene dibromide, and 60.6 g of tri-ethylamine is dissolved in 350 cc of anhydrous xylene and refluxed for about 16 hours. Thereafter the triethylamine dibromide salt formed Is separated from the solution by filtering the cool reaction mixture and washing with ether. The solution is then concentrated under reduced pressure to dryness to remove the ether, xylene and excess triethylamines present. [Pg.1176]

Ethylamine, 338 W-Ethyl acetamide, 338 Ethyl bromide, 328 reactions of, 330 Ethyl iodide, 336 Ethylene, 346 chemical reactivity, 296 double bond in, 296 Ethylene glycol, 325 Ethyl group, 329 Europium, properties, 412 Exothermic reaction, 40, 135 Experiment, 2... [Pg.459]

Ether, chloromethyl methyl [Methane, chloromethoxy-], 97 Ethylamine, dusoptopyl- [ 2-Propanamme, Af-ethyl-Af-(l-methylethyl)-], 59 Ethylamine, 2-(3,4-dimethoxyphenyl)-[Ben-zeneethanamme, 3,4-dimethoxy-], 5 Ethylene, 1,1-diphenyl- [Benzene, 1,1 -ethenylidenebis-], 32 Ethylene, tetramethyl- [2-Butene, 2,3-dimethyl-], 35... [Pg.140]

Ethoxylcarbonyl-2-arylazo-2-nitroe thane derivatives lb 365 Ethoxyquine la 106,108 Ethylamine lb 104,268 N-Ethylamine derivatives, tertiary lb 290 Ethylamphetamines la 45 N-Ethyl-N -benzylthiourea lb 301 N-Ethyl derivatives lb 190 -, secondary lb 190 -, tertiary lb 188, 191 Ethelenediamine la 392 Ethylene glycol dinitrate lb 415 N4-Ethyl-N4-(2-methanesulfonamido-ethyl)-2-methyl-l,4-phenylenediamine, reagent la 368... [Pg.485]

It is difTicult to choose between groups when using the Hass table the substance can belong to group 4 (ethylamine) or 7 (ethylene glycol) or even 8 (ethanol). [Pg.65]

Dinitrobenzenes Dinitrotoluenes 1,4-Dioxane Esters Ethylamine Ethers Ethylene Nitric acid Nitric acid Silver perchlorate Nitrates Cellulose, oxidizers Oxidizing materials, boron triiodide Aluminum trichloride, carbon tetrachloride, chlorine, nitrogen oxides, tetrafluo-roethylene... [Pg.1477]

The direct high-pressure animation of ethylene with ammonia to give ethylamine occurs in the presence of acidic zeolite catalysts such as H-elinoptilolite, H-erionite or H-offretite38. Primary amines R1NH2(R1 = Bu, cyclohexyl, PhCH2, Ph or Ar) have been monoalkylated by reaction with di-t-butyl dicarbonate, followed by successive treatment of... [Pg.538]

DIMETHYL SULFOXIDE ETHYLENE GLYCOL DIMETHYL SULFATE DIMETHYL SULFIDE ETHYL MERCAPTAN DIMETHYL DISULFIDE DIMETHYLAMINE ETHYLAMINE MONOETHANOLAMINE ETHYLENEDIAMINE DIMETHYL SILANE CYANOGEN... [Pg.7]

Chemical/Physical. Reacts with OH radicals possibly forming acetaldehyde or acetamide (Atkinson et al, 1978). When ethylamine over kaolin is heated to 600 °C, hydrogen and acetonitrile formed as the major products. Trace amounts of ethylene, ammonia, hydrogen cyanide, and methane were also produced. At 900 °C, however, acetonitrile was not produced (Hurd and Carnahan, 1930). [Pg.560]

Methamidophos, see Acephate Methane, see Acetaldehyde, Benzoic acid, 7 Bromobenzoic acid. 3-Bromobenzoic acid. 4-Bromobenzoic acid. Bromoform, Carbatyl, Catechol, 2-Chlorobenzoic acid. 3-Chlorobenzoic acid. Chloroform, Dibromochloromethane, 2,5-Dichlorobenzoic acid. 1,2-Dichloroethane, Ethylamine, Ethyl bromide. Ethylene dibromide, Ethylenimine, Formic acid, Hydroqninone, 4 Hvdroxvbenzoic acid. Indole, 2-Iodobenzoic acid. 3 lodobenzoic acid. Methyl bromide, 4-Iodobenzoic acid. 2-Methylphenol, 4-Methylphenol, Phenol, Prorocatechuic acid. Svringic acid. Svringaldehvde. TCDD, Tetrachloroethylene, Toluene, Trichloroethylene, Vanillin. Vanillic acid. Vinyl chloride... [Pg.1534]

A mixture of AN and water forms a low-strength explosive referred to as a slurry or emulsion explosive. Since a mixture of AN and water cannot be detonated by initiation with a moderate detonation strength, to formulate practical slurry explosives nitrate esters such as monomethylamine nitrate, ethylene glycol mononitrate, or ethylamine mononitrate in conjunction with aluminum powder are added as sensitizers that facilitate the initiation of detonation. [Pg.262]

Ethyl Diethanolamine and Derivatives Ethyl Diethanolamine (EDEtA), C2H5N(CH2CH2OH)2 mw 133-19, N 10.52%, colorless liq with amine odor, sp gr 1.015 at 20° nD 1.4663 at 20° bp 251-52° flash p 255°F, sol in water ale prepd by adding ethylene oxide to a cold solution of ethylamine. It is used as solvent and in detergents Refs 1) Beil. 4, 28 4 2) L. Knorr W. Scbmidt,... [Pg.98]

Ethyl-3-methylpyridine (also known as aldehyde-collidine ) has been prepared by heating aldehyde-ammonia aldehyde-ammonia and acetaldehyde or paraldehyde aldol-ammonia and ammonia paraldehyde and ammonia <> 11,12 acetamide,1 or acetamide and phosphorus pentoxide ethylene glycol and ammonium chloride ethylidene chloride or bromide and ammonia ethylidene chloride and acetamide, ethylamine, or n-amylamine crotonic acid and a calcium chloride-ammonia complex 1 and by passage of acetylene or acetaldehyde and ammonia over alumina and other catalysts. [Pg.22]

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