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Propyl propionate, oxidation

Cocoalkyl)-1 -benzyl-1 -(2-hydroxyethyl)-2-imidazolinium chloride. See Cocoyl benzyl hydroxyethyl imidazolinium chloride Cocoalkyl dimethyl benzyl ammonium chloride. See Cocoalkonium chloride N-Cocoalkyl-1,1 -iminobis-2-propanol. See PPG-2 cocam ine Coco amide. See Cocamide Coco amides, N-[3-(dimethylamino) propyl], N-oxide. See Cocamidopropylamine oxide Cocoamido betaine Cocoamidopropyl betaine. See Cocamidopropyl betaine Cocoamidopropyidimethylamine. See Cocamidopropyl dimethylamine Cocoamidopropyidimethylamine oxide. See Cocamidopropylamine oxide Cocoamidopropyidimethylamine propionate. See Cocamidopropyl dimethylamine propionate... [Pg.1013]

Hexadecanamide, N-[3-(dimethylamino) propyl]-N-oxide. See Palmitamidopropylamine oxide Hexadecanamide, N-(3-dimethylamino) propyl-, propanoate. See Palmitamidopropyl dimethylamine propionate Hexadecanamide, N-(2-hydroxyethyl)-. See Palmitamide MEA Hexadecanamide, N-[2-hydroxy-1-(hydroxymethyl) pentadecyl]-. See Palmitamidohexadecanediol Hexadecanamide, N-9-octadecenyl-. See Oleyl palmitamide... [Pg.1996]

ETHYLENE GLYCOL ETHYL MERCAPTAN DIMETHYL SULPHIDE ETHYL AMINE DIMETHYL AMIDE MONOETHANOLAMINE ETHYLENEDIAMINE ACRYLONITRILE PROPADIENE METHYL ACETYLENE ACROLEIN ACRYLIC ACID VINYL FORMATE ALLYL CHLORIDE 1 2 3-TRICHLOROPROPANE PROPIONITRILE CYCLOPROPANE PROPYLENE 1 2-DICHLOROPROPANE ACETONE ALLYL ALCOHOL PROPIONALDEHYDE PROPYLENE OXIDE VINYL METHYL ETHER PROPIONIC ACID ETHYL FORMATE METHYL ACETATE PROPYL CHLORIDE ISOPROPYL CHLORIDE PROPANE... [Pg.942]

Propene Propene Oxide Propene Polymer Propenoic Acid Beta-Propiolactone Propionaldehyde Propionic Acid Propionic Aldehyde Propionic Anhydride Beta-Propionolactone Propionyl Oxide N-Propyl Acetate 2-Propyl Acetate Propyl Alcohol... [Pg.79]

Compound Name N-Propyl Mercaptan Isopropyl Mercaptan N-Propyl Mercaptan Isopropyl Mercaptan Glycerine Propionic Acic Propionic Anhydride N-Propyl Alcohol Isopropyl Alcohol Beta-Propiolactone Acetone Acrolein Allyl Alcohol Acrylamide Propylene Propylene Oxide Polypropylene Acrylic Acid Beta-Propiolactone Propionaldehyde Propionic Acid Propionaldehyde Propionic Anhydride Beta-Propiolactone Propionic Anhydride N-Propyl Acetate Isopropyl Acetate N-Propyl Alcohol Isopropyl Alcohol N-Propyl Alcohol Propionaldehyde N-Butyl Alcohol Propylene... [Pg.79]

Mixed ethers result when alcohols and phenols are used with thoria at 390°—420° and esterification takes place when alcohol and acid interact at 350°-400°. Esterification10 is more complete in the presence of titanic oxide at 280°—300°. One molecule of acid is used with twelve molecules of alcohol, and in this way methyl, ethyl, propyl, butyl, and benzyl esters have been prepared from acetic, propionic and butyric acids. [Pg.98]

The effect of the particular functional group on adsorption, however, is not always the same as seen on oxide surfaces. For example, carboxylic acids adsorb strongly on metal oxide surfaces, and the heat of adsorption of stearic acid is higher than that of the corresponding ester, methyl stearate (Hironaka et al., 1978). For adsorption on the nascent surface, however, propionic acid is a poor adsorbate, and the adsorption activity of propionic acid is lower than that of methyl propionate. Although propyl amine adsorbs easily on metal oxide surfaces, the adsorption activity of propyl amine is low on the fresh steel surfaces. Also, the heat of adsorption of organic sulfides on iron oxide is less than that of esters (Forbes et al., 1970b), but the results of adsorption activity on the nascent surface were the opposite. It is thus noteworthy that the chemical nature of the nascent surface of steel is often opposite to that of oxide-covered metal surfaces, with respect to adsorption. [Pg.163]

Propyl alcohol1 shows a somewhat greater resistance to oxidation. Propionic acid is the chief product, and a good yield is obtained at platinum or lead peroxide anodes in sulphuric acid. Iso-propyl alcohol which is more easily oxidised gives a 70 per cent, yield of acetone. [Pg.69]

Propyl Alcohol.—n-Propyl alcohol offers a considerably greater resistance to electrical oxidation than methyl or ethyl alcohol, according to experiments made by Elbs and Brunner.1 Propionic acid is formed as the principal product, with a current yield of over 90%, at bright (polished) and platinized platinum anodes, as well as at lead peroxide anodes when the alcohol is electrolyzed in sulphuric-acid solution. A little propionic aldehyde also occurs at lower current densities. The formation of carbon mon- and dioxides is likewise very insignificant. [Pg.63]

If butyric acid is electrolyzed with perchlorate, according to the procedure of Hofer and Moest,2 hexane is the preponderating product there are also obtained propyl alcohol and its oxidation product, propionic aldehyde ... [Pg.89]

Propionaldehyde is produced by the oxo reaction of ethylene with carbon monoxide and hydrogen. n-Propyl alcohol is produced by hydrogenation of propionaldehyde, and propionic acid is made by oxidation of propionaldehyde. [Pg.371]

Fig. 11. The effect of temperature on the maximum rate of oxidation (in torr. min ) of esters [93]. (1) Methyl acetate. (2) Methyl formate. (3) Methyl propionate. (4) Ethyl formate. (5) Methyl butyrate. (6) Propyl formate. Fig. 11. The effect of temperature on the maximum rate of oxidation (in torr. min ) of esters [93]. (1) Methyl acetate. (2) Methyl formate. (3) Methyl propionate. (4) Ethyl formate. (5) Methyl butyrate. (6) Propyl formate.
Although the present major use of these hydrocarbons is as fuel, the tremendous possibilities offered for conversion to valuable chemicals makes it interesting to consider the research work which has been done and some of the results that have been attained. By oxidation these gases may be converted to methyl, ethyl, propyl, and butyl alcohols formaldehyde. acetaldehyde, propionaldehyde, and butryaldehyde formic, acetic, propionic, and butyric acids resins etc. An idea of the potentialities of hydrocarbon oxidation may be obtained by considering the theoretical yields of alcohols... [Pg.153]

Oxidation of di-rc-propyl ketone (110—120° C) produces butyric and propionic acids in equimolar amounts [125,126], The sequence of reactions is suggested to be... [Pg.155]

Phenyl propionate Copper chromium oxide 250 2,200 Propyl alcohol and cyclohexanoi 4... [Pg.584]

Propionic acid—CHs,CH2—COOH—is formed by the action of caustic potassa upon sugar, starch, gum, and ethyl cyanid during fermentation, vinous or acetic in the distillation of wood during the putrefaction of peas, beans, etc. by the oxidation of normal propylic alcohol, etc. It is best prepared by heating ethyl cyanid with potash until the odor of the ether has disappeared the acid is then liberated from its potassium compound by HjS04 and purified. [Pg.258]

Dimethylaminopropyl behenamide. See Behenamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] cocamide lactate. See Cocamidopropyl dimethylamine lactate N-[3-(Dimethylamino) propyl] coco amides. See Cocamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] coco amides-N-oxide. See Cocamidopropylamine oxide N-[3-(Dimethylamino) propyl] coco amides, propionates. See Cocamidopropyl dimethylamine propionate N-(3-Dimethylaminopropyl)-N,N-diisopropanolamine. See N,N-(Dimethyl)-N, N -diisopropanol-1,3-propanediamine N-[3-(Dimethylamino) propyl] docosanamide. See Behenamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] dodecanamide. See Lauramidopropyl dimethylamine... [Pg.1399]

N-[3-(Dimethylamino) propyl] dodecanamide-N-oxide. See Lauramidopropylamine oxide N-[3-(Dimethylamino) propyl] hexadecanamide N-[3-(Dimethylamino) propyl] hexadecan-1-amide. See Palmitamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] hexadecanamide-N-oxide. See Palmitamidopropylamine oxide [R-(Z)]-N-[3-(Dimethylamino) propyl]-12-hydroxy-9-octadecenamide. See Ricinoleamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] isooctadecanamide. See Isostearamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] isooctadecanamide, N-oxide. See Isostearamidopropylamine oxide Dimethylaminopropyl lauramide. See Lauramidopropyl dimethylamine Dimethylaminopropyl lauramide propionate. [Pg.1400]

N-[3-(Dimethylamino) propyl]-9-octadecenamide-N-oxide. See Oleamidopropylamine oxide Dimethylaminopropyl oleamide N-[3-(Dimethylamino) propyl] oleamide. See Oleamidopropyl dimethylamine Dimethylaminopropyl oleamide glycolate. See Oleamidopropyl dimethylamine glycolate Dimethylaminopropyl oleamide lactate. See Oleamidopropyl dimethylamine lactate N-[3-(Dimethylamino) propyl] olive amides. See Olivamidopropyl dimethylamine N-[3-(Dimethylamino) propyl] olive amides-N-oxide. See Olivamidopropylamine oxide Dimethylaminopropyl palmitamide. See Palmitamidopropyl dimethylamine Dimethylaminopropylpalmitamide lactate. See Palmitamidopropyl dimethylamine lactate Dimethylaminopropylpalmitamide propionate. See Palmitamidopropyl dimethylamine propionate... [Pg.1400]

Lauramidopropyl dimethylamine oxide. See Lauramidopropylamine oxide Lauramidopropyl dimethylamine propionate CAS 67801-62-1 EINECS/ELINCS 267-182-3 Synonyms Dimethylaminopropyl lauramide propionate Propionic acid, compd. with N-[3-(dimethylamino) propyl] dodecanamide (1 1) Definition Propionic acid salt of lauramidopropyidimethylamine Empirical C17H36N2O C3H6O2 Formula ... [Pg.2338]

Oleamidopropyl dimethylamine oxide. See Oleamidopropylamine oxide Oleamidopropyl dimethylamine propionate CAS 67801-61-0 EINECS/ELINCS 267-181-8 Synonyms Dimethyl [3-(oleoylamino) propyl] ammonium propionate Classification Organic salt Empirical C23H46N20 C3He02 Uses Antistat in cosmetics... [Pg.2968]


See other pages where Propyl propionate, oxidation is mentioned: [Pg.1603]    [Pg.1604]    [Pg.464]    [Pg.953]    [Pg.92]    [Pg.968]    [Pg.1539]    [Pg.65]    [Pg.899]    [Pg.85]    [Pg.954]    [Pg.489]    [Pg.90]    [Pg.290]    [Pg.114]    [Pg.56]    [Pg.45]    [Pg.1483]   
See also in sourсe #XX -- [ Pg.179 ]




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Propionic oxidation

Propyl oxidation

Propyl propionate

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