Esters isopropyl acetate

SYNS BENZYL ISOVALERATE (FCC) BENZYL-3-METHYLBUTANOATE BENZYL-3-METHYL BUTYRATE FEMA No. 2152 ISOPENTANOIC ACID, PHENYLMETHYL ESTER ISOPROPYL ACETIC ACID, BENZYL ESTER 3-METHYLBUTANOIC ACID, PHENYLETHYL ESTER... 

Synonyms Benzyl 3-methyl butanoate Benzyl 3-methyl butyrate Isopentanoic acid, phenylmethyl ester Isopropyl acetic acid, benzyl ester Isovaleric acid, benzyl ester 3-Methylbutanoic acid, phenylethyl ester Empirical C12H16O2... 

Methyl, ethyl, n-propyl, isopropyl, n-hutyl, benzyl, cyclohexyl esters of formic, acetic, oxalic, succinic, tartaric, citric, benzoic, salicylic (and other substituted benzoic acids), phthalic and cinnamic acids phenyl esters of acetic, benzoic and salicylic acids. 

Olefins add anhydrous acetic acid to give esters, usually of secondary or tertiary alcohols propjiene [115-07-1] yields isopropyl acetate [108-21-4], isobutjiene [115-11-7] gives tert-huty acetate [540-88-5]. Minute amounts of water inhibit the reaction. Unsaturated esters can be prepared by a combined oxidative esterification over a platinum group metal catalyst. Eor example, ethylene-air-acetic acid passed over a palladium—Hthium acetate catalyst yields vinyl acetate. 

Ketones and esters are required for C-type inks. Types of esters are ethyl acetate, isopropyl acetate, normal propyl acetate, and butyl acetate. From the ketone class, acetone or methyl ethyl ketone (MEK) can be used. The usual solvent for D-type inks are mixtures of an alcohol, such as ethyl alcohol or isopropyl alcohol, with either aUphatic or aromatic hydrocarbons. Commonly used mixtures are 50/50 blends by volume of alcohol and aUphatic hydrocarbon. 

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. 

Unsaturated Hydrocarbons. Olefins from ethylene through octene have been converted into esters via acid-catalyzed nucleophilic addition. With ethylene and propjiene, only a single ester is produced using acetic acid, ethyl acetate and isopropyl acetate, respectively. With the butylenes, two products are possible j -butyl esters result from 1- and 2-butylenes, whereas tert-huty esters are obtained from isobutjiene. The C5 olefins give rise to three j iC-amyl esters and one /-amyl ester. As the carbon chain is lengthened, the reactivity of the olefin with organic acids increases. 

Acetate Esters Methyl acetate Ethyl acetate Propyl acetate Isopropyl acetate Butyl acetate Isobutyl acetate Amyl acetate... 

Chemical Designations - Synonyms Butoxyethyl 2,4-Dichlorophenoxyacetate Butyl 2,4-Dichlorophenoxyacetate 2,4-Dichlorophenoxyacetic Acid, Butoxyethyl Ester 2,4-Dichlorophenoxyacetic Acid, Isopropyl Ester Isopropyl 2,4-Dichlorophenoxy Acetate Chemical Formula 2,4-Cl2C H30CH2C00R, where R=C4H9, CjH, or CH2CH2OC4H9. 

About 50% of isopropanol use is to produce acetone. Other important synthetic uses are to produce esters of many acids, such as acetic (isopropyl acetate, solvent for cellulose nitrate), myristic, and oleic acids (used in lipsticks and lubricants). Isopropylpalmitate is used as an emulsifier for cosmetic materials. Isopropyl alcohol is a solvent for alkaloids, essential oils, and cellulose derivatives. 

Isopropyl acetate is produced by the catalytic vapor-phase addition of acetic acid to propylene. A high yield of the ester can be realized (about 99%) ... 

The initial study of the La3 +-catalyzed methanolysis of carboxylate esters163 reported the apparent second-order rate constant for La2 + ( OCH3)2-catalyzed methanolysis of some representative examples of aryl esters (2, 5 and 2,4-dinitrophenyl acetate (14)), phenyl benzoate (15) and three aliphatic esters, ethyl acetate, isopropyl acetate (16) and tert-butyl acetate (17). Given in Table 6 are the rate constants for the La3+ and methoxide-catalyzed methanolysis of these esters along with... 

This stereospecific oxidation does not occur for all dioximes, probably due to isomerisation of the dioxime during the reaction or to different reaction mechanisms involved in the use of different oxidants. When the lipophilic-hydrophilic balance of the two furoxan isomers is appropriate, they are easily separated by chromatography or fractional crystallisation. For example, the synthesis of 4-hydroxymethyl-3-furoxancarboxamide (CAS 1609), one of the most promising furoxancarboxamide vasodilators (see later), passes through the intermediate formation of a mixture of the two isomeric methyl hydroxymethylfuroxancarboxylic esters, which can easily be separated by recrystallisation from isopropyl acetate [18]. 

This procedure illustrates the use of lithio esters for the preparation of /3-hydroxy esters. Isopropyl and /-butyl /3-hydroxy-/8,/3-diphenylpropionate may be prepared in approximately 80% yields by using isopropyl or /-butyl acetates in place of ethyl acetate.2 This procedure is generally more convenient than the Reformatsky reaction for the preparation of such esters. Under similar conditions ethyl acetate may conveniently be condensed with various aldehydes or ketones to give the corresponding /8-hydroxy esters.4... 

The novolac sample, which was provided by Kodak, was synthesized from pure meta-cresol and formaldehyde. It has a weight average molecular weight of 13,000 and a very broad polydispersity of 8.5. The polymer was purified by two precipitations from tetrahydrofuran into hexane. The PAC was a naphthoquinone-1,2-(diazide-2-)-5-sulfonyl ester provided by Fairmount Chemical (Positive Sensitizer 1010). A hydroxyl substituted benzophenone is attached to the sulfonyl ester. The spreading solvent was isopropyl acetate, which was obtained from Aldrich Chemicals and used as received. 

Acetic acid, 2-ethoxyethyl ester, see 2-Ethoxyethyl acetate Acetic acid, ethylene ester, see Vinyl acetate Acetic acid, ethyl ester, see Ethyl acetate Acetic acid, isobutyl ester, see Isobutyl acetate Acetic acid, isopentyl ester, see Isoamyl acetate Acetic acid, isopropyl ester, see Isopropyl acetate Acetic acid, 2-methoxyethyl ester, see Methyl cellosolve acetate... 

Acetic acid, 1-methylethyl ester, see Isopropyl acetate... 

The short-tailed fmit bat, Carollia perspicillata, discriminates the odor of ripe from that of green bananas. Odor cocktails of banana odor components were distinguished from the whole odor of banana (Laska, 1990). The two most common esters of banana odor are isopentyl acetate and isobutyl acetate. Nearly all fruit odors contain ethyl acetate. Isopropyl acetate and 2-pentanone are characteristic of putrefying fruits. 

Ester Content (as Ethyl Acetate) — min 85 0 max 88.0%. It shall be detd in accordance with ASTM D1617-69, described in Annual Book of ASTM Standards, Part 20(1972), 736-39 Note 1 The method described in ASTM D1617— 69 applies not only to EtAcet, but also to other esters, such as N-butyl acetate, isopropyl acetate, acetate ester of ethylene glycol monoethyl ether, sec-butyl acetate, amyl acetate, dibutyl phthalate and iso butyl acetate... 

ISOPROPYL ACETATE Acetic Acid, isopropyl ester, 2-Propyl acetate Flammable Liquid, II 1 3 0... 

This technique and these results have been extended in a very complete investigation by Yates and McClelland37. These authors have measured the rates of hydrolysis of eight representative acetate esters in 10-100% sulphuric acid some of their results are plotted in Fig. 1, (p. 74.) Yates and McClelland also measured the protonation behaviour of three of the esters in the same medium, by the spectrophotometric method (p. 70). They found that the basicities of the three esters, methyl, -propyl and isopropyl acetate, are closely similar, and that their protonation behaviour is described by the equation37... 

Fatty acid esters Ethyl acetate, methyl methacrylate, trimethylolpropane trimethacrylate, decyl methacrylate, 2-hydroxyethyl methacrylate, ethoxy ethyl acetate, methyl palmitate, ethyl palmitate, isopropyl palmitate, butyl palmitate, isobutyl palmitate, methyl margarate, butyl margarate, methyl stearate, ethyl stearate, butyl stearate, isobutyl stearate, methyl oleate, bis(2-ethylhexyl) adipate, bis(2-ethylhexyl) sebacate, methyl linoleate, methyl laurate, octyl laurate, methyl myristate, isobutyl myristate, butyl myristate, dihydroisopimaric add methyl ester... 

To a 5 L 3-neck round bottom flask was added the crude carbonylbenzyloxy-3-aminopropanal (115 g, 0.555 mol) followed by addition of water (400 mL) and methanol (1600 mL). The reaction mixture was maintained at 25°C throughout the course of the reaction. After the solution became homogeneous. (S)-Valine methyl ester hydrochloride (90.2 g, 0.538 mol) was added in one portion followed by rapid addition of sodium acetate trihydrate (151 g, 1.11 mol) and sodium cycanoborohydride (73.2 g, 1.17 mol). The reaction mixture was allowed to stir at room temperature for 0.5 hour and was concentrated in vacuo. To this solution, saturated aq sodium bicarbonate (400 mL) was added and the mixture was extracted with isopropyl acetate (1 L). The organic layer was washed with water, dried over sodium sulfate, and concentrated to yield 150 g of crude product, which was dissolved in isopropyl acetate (300 mL) and heptane (2400 mL). Dry HCI was bubbled in and an oily solid precipitated out of solution. The liquid was decanted away from and the solid was dissolved in dichloromethane (3 L). The solution was washed with water (600 mL) and saturated aq sodium bicarbonate (600 mL) and dried over sodium sulfate. It was concentrated in vacuo to yield 105 g (59%) of N-(N-(benzyloxycarbonyl-3-amino)-propyl)valine methyl ester as a light yellow oil. 

To a 12 L 3-neck round bottom flask with stir bar was added 2S-(1-tetrahydro-pyrimid-2-onyl)-3-methyl butanoic acid methyl ester (126 g, 0.588 mol), water (1.3 L), and THF (3.9 L). The solution was cooled to 0°C in an ice-water bath and lithium hydroxide monohydrate (74 g, 1.76 mol) was added in one portion with rapid stirring. The solution was allowed to stir at 0°C for 14 hours. It was then acidified to pH 11 by slow addition of 50% aq. phosphoric acid and the THF was removed in vacuo. The aqueous phase was washed with isopropyl acetate (2 L) and was subsequently acidified to pH by slow addition of 35% aq. HCI. The aqueous layer was then extracted with ethyl acetate. The combined organic layers were concentrated to give the desired product (105 g) as a white solid. The compound was then purified by... 

Esters with fewer than five carbon atoms Isopropyl acetate Ethers... 

All the spectroscopic approaches applied for structural characterization of mixtures derive from methods originally developed for screening libraries for their biological activities. They include diffusion-ordered spectroscopy [15-18], relaxation-edited spectroscopy [19], isotope-filtered affinity NMR [20] and SAR-by-NMR [21]. These applications will be discussed in the last part of this chapter. As usually most of the components show very similar molecular weight, their spectroscopic parameters, such as relaxation rates or selfdiffusion coefficients, are not very different and application of these methodologies for chemical characterization is not straightforward. An exception is diffusion-edited spectroscopy, which can be a feasible way to analyze the structure of compounds within a mixture without the need of prior separation. This was the case for the analysis of a mixture of five esters (propyl acetate, butyl acetate, ethyl butyrate, isopropyl butyrate and butyl levulinate) [18]. By the combined use of diffusion-edited NMR and 2-D NMR methods such as Total Correlation Spectroscopy (TOCSY), it was possible to elucidate the structure of the components of this mixture. This strategy was called diffusion encoded spectroscopy DECODES. Another example of combination between diffusion-edited spectroscopy and traditional 2-D NMR experiment is the DOSY-NOESY experiment [22]. The use of these experiments have proven to be useful in the identification of compounds from small split and mix synthetic pools. 

Esters Ethyl formate Propyl formate Methyl acetate Ethyl acetate Propyl acate Isopropyl acetate hco-o-c2h5 hco-o-c3h7 CH3-CO-0-CH3 ch3-co-o-c2h5 ch3-co-o-c3h7 CH3-C0-0-CH(CH3)2... 

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