Ethyl acetate butyrate

Recovery of aroma compounds (l-octene-3-ol, ethyl acetate/butyrate/hexanoate) Recovery of picolines from aqueous solutions Recovery of aroma compounds... 

Chem. Descrip. Ethoxyethanol CAS 1KT80-5 EINECS/ELINCS 203-804-1 Uses Solvent tor coatings (NC, ethyl acetate, butyrate, acrylic, water-sol.)... 

Methyl formate. Ethyl formate Methyl acetate Iso-propyl formate Ethyl acetate Methyl propionate "-Propyl formate Iso-propyl acetate Methyl iso-butyrate Iso-butyl formate. Ethyl propionate M-Propyl acetate. Methyl butyrate. ... 

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... 

Ethyl n-butyrate. Use a mixture of 88 g. (92 ml.) of n-butyric acid, 23 g. (29 ml.) of ethanol and 9 g. (5 ml.) of concentrated sulphuric acid. Reflux for 14 hours. Pour into excess of water, wash several times with water, followed by saturated sodium bicarbonate solution until all the acid is removed, and finally with water. Dry with anhydrous magnesium sulphate, and distU. The ethyl n-but3rrate passes over at 119 5-120-5°, Yield 40 g. An improved yield can be obtained by distilhng the reaction mixture through an efficient fractionating column until the temperature rises to 125°, and purifying the crude ester as detailed above under methyl acetate. 

Only esters containing two a-hydrogen atoms (ethyl acetate, propionate, n-butyrate, etc.) can be condensed with the aid of sodium alkoxides. For esters with one a-hydrogen atom, such as ethyl tsobutyrate, the more powerful base sodium triphenylmethide PhaC Na leads to condensation with the formation of ethyl a-tsobutyrylisobutyrate ... 

The formation of acyloins (a-hydroxyketones of the general formula RCH(OH)COR, where R is an aliphatic residue) proceeds best by reaction between finely-divided sodium (2 atoms) and esters of aliphatic acids (1 mol) in anhydrous ether or in anhydrous benzene with exclusion of oxygen salts of enediols are produced, which are converted by hydrolysis into acyloins. The yield of acetoin from ethyl acetate is low (ca. 23 per cent, in ether) owing to the accompanying acetoacetic ester condensation the latter reaction is favoured when the ester is used as the solvent. Ethyl propionate and ethyl ji-butyrate give yields of 52 per cent, of propionoin and 72 per cent, of butyroin respectively in ether. 

Butane-Naphtha Catalytic Liquid-Phase Oxidation. Direct Hquid-phase oxidation ofbutane and/or naphtha [8030-30-6] was once the most favored worldwide route to acetic acid because of the low cost of these hydrocarbons. Butane [106-97-8] in the presence of metallic ions, eg, cobalt, chromium, or manganese, undergoes simple air oxidation in acetic acid solvent (48). The peroxidic intermediates are decomposed by high temperature, by mechanical agitation, and by action of the metallic catalysts, to form acetic acid and a comparatively small suite of other compounds (49). Ethyl acetate and butanone are produced, and the process can be altered to provide larger quantities of these valuable materials. Ethanol is thought to be an important intermediate (50) acetone forms through a minor pathway from isobutane present in the hydrocarbon feed. Formic acid, propionic acid, and minor quantities of butyric acid are also formed. 

PMMA is not affected by most inorganic solutions, mineral oils, animal oils, low concentrations of alcohols paraffins, olefins, amines, alkyl monohahdes and ahphatic hydrocarbons and higher esters, ie, >10 carbon atoms. However, PMMA is attacked by lower esters, eg, ethyl acetate, isopropyl acetate aromatic hydrocarbons, eg, benzene, toluene, xylene phenols, eg, cresol, carboHc acid aryl hahdes, eg, chlorobenzene, bromobenzene ahphatic acids, eg, butyric acid, acetic acid alkyl polyhaHdes, eg, ethylene dichloride, methylene chloride high concentrations of alcohols, eg, methanol, ethanol 2-propanol and high concentrations of alkahes and oxidizing agents. 

Amino alcohols can be resolved by a number of pathways including hydrolysis, esterification, and transesterification. For example, hydrolysis of Ai,0-diacet5l-2-amino-l-butanol with PPL followed by recrystallization results in (80a) with 95% ee (108). Hydrolysis of racemic acetates or butyrates of 2-[(aLkoxycarbonyl)amino]-l-aLkanols with PFL gives (R)-alcohol (81) with 95% ee (109). (3)-(81) can be obtained by transesterification of the racemic (81) with ethyl acetate which also serves as the reaction medium (109). 

Esters of medium volatility are capable of removing the water formed by distillation. Examples are propyl, butyl, and amyl formates, ethyl, propyl, butyl, and amyl acetates, and the methyl and ethyl esters of propionic, butyric, and valeric acids. In some cases, ternary azeotropic mixtures of alcohol, ester, and water are formed. This group is capable of further subdivision with ethyl acetate, all of the ester is removed as a vapor mixture with alcohol and part of the water, while the balance of the water accumulates in the system. With butyl acetate, on the other hand, all of the water formed is removed overhead with part of the ester and alcohol, and the balance of the ester accumulates as a high boiler in the system. 

To a solution of 42.0 g of p-[N-bis(/3-chloroethyl)amino] phenyl butyric anhydride in 500 ml dry pyridine was added 24.4 g of prednisolone. The reaction mixture was kept at room temperature for 24 hours under anhydrous condition. It was then poured into a mixture of concentrated HCI and crushed ice and extracted with ether-ethyl acetate (1 1). 

Cellulosic They are tough, transparent, hard or flexible natural polymers made from plant cellulose feedstock. With exposure to light, heat, weather and aging, they tend to dry out, deform, embrittle and lose gloss. Molding applications include tool handles, control knobs, eyeglass frames. Extrusion uses include blister packaging, toys, holiday decorations, etc. Cellulosic types, each with their specialty properties, include cellulose acetates (CAs), cellulose acetate butyrates (CABs), cellulose nitrates (CNs), cellulose propionate (CAPs), and ethyl celluloses (EC). 

Besides butanol and ethanol ethyl acetate, ethyl butyrate and butyl butyrate was detected in the reaction mixture. 

Cellulose acetate resin Cellulose-acetate-propionate resin Cellulose-acetate-butyrate resin Cellulose nitrate resin Ethyl cellulose resin Rayon... 

Cellulose- acetate butyrate resin, molding Cellulose-acetate propionate resin, molding Ethyl cellulose Cellulose nitrate ... 

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... 

Cellulose derived-acetate, acetate butyrate, ethyl, nitrate Chlorinated rubbers... 

Ethoxylated Dodecanol Ethoxylated Dodecyl Alcohol Ethoxylated Myristyl Alcohol Ethoxylated Nonylphenol Ethoxylated Pentadecanol Ethoxylated Pentadecyl Alcohol Ethoxylated Tetradecanol Ethoxylated Tetradecyl Alcohol Ethoxylated Tridecanol Ethoxylated Tridecyl Alcohol Ethoxytriethylene Glycol Ethoxy Triglycol Ethyl Acetate Ethylacetic Acid Ethyl Acetoacetate Ethyl Acrylate Ethyl Alcohol Ethyl Aldehyde Ethylaluminum Dichloride Ediylaluminum Sesquichloride Ethylamine Ethylbenzene Ethyl Butanoate Ethyl Butanol 2-Ethyl-1 -Butanol 2-Ethylbutyl Alcohol Ethyl Butyrate... 

Inert binders Polybutadiene and cellulose derivatives are used as binders for LOVA formulations [24]. The commonly used polybutadiene-based binders are hydroxy-terminated polybutadiene (HTPB) and carboxy-terminated polybutadiene (CTPB)/poly(butadiene-acrylonitrile) (PBAN) while the most commonly used cellulose derivatives are ethyl cellulose (EC), cellulose acetate (CA), cellulose acetate butyrate (CAB) and cellulose... 

Objects molded from classic ABS or ASA copolymers are generally severely attacked by numerous chemical products, such as acids like acetic acid, butyric acid, and nitric acid, phthalates like dioctyl phthalate, gasoline, greases, inks, iodine, alcohols like methanol, motor oils, phenols, glycols, tetrachloroethylene, and acetates like ethyl acetate, amyl acetate, and others (29). 

Ethyl isobutyrylisobutyrate. Add 24-6 g. (28-3 ml.) of ethyl iso-butyrate, b.p. 110-111°, to the solution of ca. 0 21 mol of sodium triphenyl-methide in approximately 1400 ml. of ether contained in the 2-litre conical flask. Stopper the flask, shake well to effect complete mixing, and keep at room temperature for 60 hours. Acidify the reaction mixture by adding, with shaking, 15 ml. of glacial acetic acid, and then extract with 100 ml. of water. Wash the ethereal solution with 50 ml. portions of 10 per cent, sodium carbonate solution until free from excess acid, dry over anhydrous magnesium sulphate, and distil off the ether on a steam bath. Distil the residue under reduced pressure from a Claisen flask with fractionating side arm (Figs. II, 24, 4—5). Collect the ethyl isobutyryl isobutyrate at 95-96°/18 mm. the yield is 15 g. The b.p. at atmospheric pressure is 201-202°. 

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