N-Propyl isobutyrate

M-Butyl formate. Ethyl iso-butyrate IsO -butyl acetate Ethyl butyrate -Propyl propionate Iso-amyl formate, -But> l acetate Iso-propyl butyrate Iso-butyl propionate n-Propyl -butyrate -Butyl propionate Iso-butyl isobutyrate Ethyl lactate Iso-butyl butyrate Cycloheicyl formate -Butyl -butyrate Iso-propyl lactate. Cyclohexyl acetate Diethyl oxalate Di-iao-propyl oxalate... 

N-VALERIC ACID ISOBUTYL FORMATE N-PROPYL ACETATE ETHYL PROPIONATE METHYL BUTYRATE METHYL ISOBUTYRATE PIPERIDINE N-PENTANE 2-METHYL BUTANE 2 2-DIMETHYL PROPANE... 

METHYL ISOBUTYL KETONE n-PENTYL FORMATE n-BUTYL ACETATE sec-BUTYL ACETATE tert-BUTYL ACETATE ETHYL n-BUTYRATE ETHYL ISOBUTYRATE ISOBUTYL ACETATE n-PROPYL PROPIONATE CYCLOHEXYL PEROXIDE DIACETONE ALCOHOL 2-ETHYL BUTYRIC ACID n-HEXANOIC ACID 2-ETHOXYETHYL ACETATE HYDROXYCAPROIC ACID PARALDEHYDE... 

Pineapple Allyl capruale, cyclohexylacetaie. cyclohexylbutyrate, cyclohexylptopionate. 2-nonylenate, phenoxyacetate Benzyl formate Bomyl acetate n-Bulyl acetate Butyl isobutyrate Cinnamyl acetate Decanal dimethyl acetal Ethyl butyrate, hexadienoate. phenoxyacetate Hexyl butyrate 2-Methylallyl capruale Methyl heia-methy Ipropionaie Methyl undecylate Propyl isobutyrate. 

The following points are to be noted. First of all, complexes 5.1, 5.3, 5.5, and 5.7 are 18-electron complexes, while the rest are 16-electron ones. Second, conversions of 5.3 to 5.4 and 5.5 to 5.6 are the two insertion steps. The selectivity towards n-butyraldehyde is determined in the conversion of 5.3 to 5.4. It is possible that a rhodium-isopropyl rather than rhodium-propyl complex is formed. In such a situation on completion of the catalytic cycle isobutyral-dehyde will be the product. In practice both the n-propyl and the /-propyl complexes of rhodium are formed, and a mixture of n-butyraldehyde and /-butyraldehyde is obtained. This aspect is discussed in greater detail in the following section. Third, the catalyst precursor 5.1 undergoes ligand dissocia-... 

Methyl hydrazine Methyl isobutyl ketone Methyl isobutyrate Methyl, mercaptan Methyl methacrylate 1 -Methylnaphthalene 2-Methyl-2-propanethiol, see t-Butyl mercaptan Methyl-n-Propyl ketone 1 -Methylpyrrole Methyl salicylate a-Methyl styrene m.-p-Methyl styrene Methyl sulphate, see Dimethyl sulphate... 

METHYLPROPYL ISOBUTYRATE see IIWOOO METHYL-n-PROPYL KETONE see PBN250 METHYL PROPYL KETONE (ACGIH, DOT) see PBN250... 

RTIY2 -F Me Sn CH3RTIY -F MejSnY where R = Me, Et, n-propyl, phenyl Y = isobutyrate and ... 

This paper deals with the synthesis of propionic acid by the reaction of carbon monoxide, ethylene, and water and the synthesis of isobutyric acid and 2-methylbutyric acid by the reaction of carbon monoxide with n-propyl alcohol and n-butyl alcohol, respectively, in presence of nickel catalysts at high pressures. 

Methyl n-propyl ketone. See Methyl propyl ketone 2-Methylpropyl methacrylate. See Isobutyl methacrylate 2-Methylpropyl methyl ketone. See Methyl isobutyl ketone 2-Methylpropyl 2-methylpropanoate. See Isobutyl isobutyrate 2-Methylpropy octadecanoate. See Isobutyl stearate 1-MethylpyiTolidinone 1-Methyl-2-pyiTolidinone N-Methylpyrrohdinone N-Methyl-2-pyrrolidinone Meth pyrrolidone 1-Methylpyrrolidone l-Methyl-2-pyrrolidone N-Methylpyrrolidone. See N-Methyl-2-pyrrolidone... 

Many acrylic copolymers are currently used in the textile industry as binders for nonwoven fabrics. The purpose of these fibers is to stabilize the material. In many instances, these copolymers are used in conjunction with amino resins. Casanovas and Rovira have done a study of methyl methacrylate-ethyl acrylate-N-methylol-acrylamide by PY/GC-MS. Among the products identified were methane, ethylene, propene, isobutene, methanol, propionaldehyde, ethanol, ethyl acetate, methyl acrylate, methyl isobutyrate, ethyl acrylate, methyl methacrylate, n-propyl acrylate, and ethyl methacrylate. In this sample, clearly monomer reversion is the primary degradation process occurring however, several other degradation mechanisms are at work. When the sample contains an amino resin in the mixture, acrylonitrile is observed in the pyrogram. Another effect of the amino presence was a marked increase in the amount of methanol detected. Other products detected were meth-oxyhydrazine, methyl isocyanate, and methyl isocyanide. 

Bromo-2-fluoro biphenyl intermediate, foam builders Alkenyl succinic anhydride intermediate, food additives Soy acid Stearyl alcohol intermediate, food emulsifiers Caprylic/capric acid Tallow acid intermediate, food supplements (tablet form) Cetyl alcohol intermediate, food wrap Vinylidene chloride monomer intermediate, fragrances p-t-Butyl toluene t-Butyl-m-xylene Citral Cyclopentanone Diethyl toluene diamine Dimethyl hexynediol 1,2-Methylenedioxybenzene 2-Methylpentanal Myrcene n-Propyl bromide intermediate, fragrances cosmetics Acetic anhydride n-Butyraldehyde n-Butyric acid Butyric anhydride 2-Ethylhexoic acid Isobutyric anhydride 2-Methylpropanal Propionic anhydride intermediate, fragrances personal care Butyric anhydride Isobutyric anhydride intermediate, free-radical polymerization initiators... 

Isobutyric acid n-Butyric acid Propylacetate Propyl- isobutyrate Propyl-n- butyrate Ratio of Isobutyric to n-Butyric acid... 

CH3COOH medium. Either C3H7I or HI is used as promoters. Conversion of CsHe is 97-100% output of by-products propylacetate, propyl-n-but3trate, and propyl-isobutyrate does not exceed 10%. Increase in the reaction temperature does not affect the conversion the rate of conversion, however, increases notably. This is evident from a reduction of duration of the experiment from 9 h at 100°C to 2.5 h at 200°C. The selectivity of catalyst with respect to the formation of butyric acids decreases (from 100 to 90%) as the temperature increases. 

Methyl acetate Ethyl formate Ethyl acetate Isopropyl acetate Methyl /i-butyrate n-Propyl acetate Isobutyl acetate n-Butyl acetate Amyl acetate Isobutyl isobutyrate Methyl amyl acetate n-Amyl acetate... 

Isobutyric Acid N-Butyric Acid Propylene Gylcol Hydroxypiopyl Acrylate 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 Beu-Propiolactone Propionic Anhydride N-Propyl Acetate Isopropyl Acetate N-Propyl Alcohol Isopropyl Alcohol N-Propyl Alcohol Propionaldehyde N-Butvl Alcohol... 

Since solubility tests are of qualitative character only, certain compounds near the border line must be listed in more than one place to avoid error. For example, several of the compounds listed on page 189 will be reported normally insoluble in water according to the standards set in Chapter TII. Such compounds, therefore, will be found also in the water-insoluble groups, e.g.. Methyl isobutyrate, ethyl propionate, and n-propyl acetate are listed in V, 5 methyl propyl ketone and diethyl ketone in V, 3, etc. 

The products were isolated as esters by reaction of the acylcobalt carbonyls with an alcohol and iodine. In the case of the alkyl halides, carbon monoxide was normally absorbed, but under nitrogen, acylcobalt tricarbonyls must be formed. The reaction with alkyl halides was slow and some isomerization was noted using M-propyl iodide (formation of n-butyrates and isobutyrates). Absence of carbon monoxide promoted the isomerization. Isopropyl iodide gave no reaction. When ethyl a-bromopropionate was used, no isomerization was found at — 25 °C under carbon monoxide, but the isomerized product, diethyl succinate, was the major product at 25° C under carbon monoxide or nitrogen. Under the conditions of the experiments no isomerization of the alkyl halide itself was found. 

With stirring, 44.1 g of isobutyric acid is added to a mixture of 51.0 g of diisopropylamine, 23.2 g of a 57% sodium hydride dispersion in mineral oil, and 350 ml of tetrahydrofuran. When gas evolution subsides, the mixture is heated at reflux for 15 minutes, cooled to 0°C, and treated with 345 ml of a 1.45M solution of n-butyl lithium in heptane. After 5 hr, the mixture is warmed one-half hour at 30°C, cooled to 0°C, and treated with 122.0 g of 3-(2,5-xylyloxy)propyl bromide. After one more hour, it is stirred with 500 ml of water and the aqueous phase is separated and acidified with 150 ml of 6N... 

Petersen1 was able to obtain n-hexane and propyl butyrate in small quantity from butyric acid from isobutyric acid he got diisopropyl (isohexane) in addition to the products observed by Hamonet. 

The products of methyl n-hexyl ketone oxidation are capronic and acetic acids, capronic aldehyde, and diketone (130°C) [126], The hydroperoxide formed by the oxidation of di-iso-propyl ketone is relatively stable [127]. Decay of hydroperoxide produces acetone and isobutyric acid... 

The products of the reactions of carbon monoxide with w-propyl alcohol and n-butyl alcohol, respectively, consisted mainly of isobutyric acid (m.p. and mixed m.p. of p-toluidide 104-105°) and 2-methylbutyric acid (m.p. and mixed m.p. of anilide 108-109°, m.p. of p-toluidide, 92-93°) and small... 

Propanoic acid butyl ester. See n-Bulyl propionate Propanoic acid, ethenyl ester. See Vinyl propionate Propanoic acid ethyl ester. See Ethyl propionate Propanoic acid, 2-hydrorqr-. See Lactic acid Propanoic acid, 2-hydrorqr-, ammonium salt SeeAmmonium lactate Propanoic acid, 2-hydrorqr-, butyl ester. See Butyl lactate Propanoic acid, 2-hydrorqr-, 1-methylethyl ester. See Isopropyl lactate Propanoic acid, 2-methyl-, monoester with 2,2,4-trimethyl-1,3-pentanediol. See2,2,4-Trimethyl-1,3-pentanediol isobutyrate Propanoic acid, pentyl ester. SeeAmyl propionate Propanoic acid, propyl ester. See Propyl propionate Propanoic acid, 3,3 -thiobis-, dioctadecyl ester. See Disteatyl thiodipro-pionate... 

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