ライフサイエンスコーパス: ethyl acetate

1 de groups, consistent with poly(methylene-co-ethyl acetate).

2 , and many oils (decane, petroleum ether, or ethyl acetate).

3 ion through the formation of an organogel in ethyl acetate.

4 o acetic acid, which increased together with ethyl acetate.

5 hree solvents: D(2)O, acetonitrile-d(3), and ethyl acetate.

6 lcohols, acetonitrile, acetone, toluene, and ethyl acetate.

7 ost potent mushroom chemicals are soluble in ethyl acetate.

8 olesteryl N-(2-naphthyl) carbamate (CeNC) in ethyl acetate.

9 wed by hydrogenation in a mixture of ethanol/ethyl acetate.

10 dioactivity in the plasma not extractable by ethyl acetate.

11 system with water and either nitromethane or ethyl acetate.

12 tyrate (EB), propionic acid, 2-butanone, and ethyl acetate.

13 st conversion rates compared to acetic acid, ethyl acetate.

14 ble matrix compounds and the extraction with ethyl acetate.

15 d with hexane to be further partitioned into ethyl acetate.

16 emonstrated an increase in the production of ethyl acetate.

17 osulfur 'flavour' molecules is achieved with ethyl acetate.

18 tridge, followed by OTA elution with 1 mL of ethyl acetate.

19 t as effective as acetonitrile, acetone, and ethyl acetate.

20 of fractions from Rosmarinus officinalis L.: ethyl acetate 1 and 2 (AcOEt1 and 2), hexane (HEX), etha

21 sor for preparation of (13) C hyperpolarized ethyl acetate-1-(13) C, which provides a convenient vehi

22 uated by measuring the (13)C polarization of ethyl acetate-1-(13)C, i.e., the product of pairwise add

23 [viz., 2-(1,5,5-trimethylcyclopent-2-en-1-yl)ethyl acetate] (1) is described.

24 nvolved extraction of 10 g sample with 10 ml ethyl acetate (+10 g sodium sulphate) by homogenization

25 orm (1b); toluene (1c); and diethyl ether or ethyl acetate (1d), demonstrate different photoluminesce

26 tyrolactone, isoamyl alcohols, acetaldehyde, ethyl acetate, 2,3-butanediol, acetoin and 2,3-butanedio

27 Metabolization of ethyl acetate, 2,3-pentanedione, benzaldehyde, and 2-fur

28 bolites, ethanol, acetaldehyde, acetic acid, ethyl acetate, 2-butanone, 2,3,-butanedione, and acetone

29 The content of 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol a

30 ged and extra-aged tequila using 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol a

31 elow the taster's threshold detection limit: ethyl acetate 39.48 ng mL(-1) (RSD mean value 4.2%), iso

32 e moment - hexane: 0.0, diethyl ether: 2.80, ethyl acetate: 4.40, methanol: 5.10 and water: 9.0D) wer

33 lpha-[1-[2,6-dimethoxy-4-(2-propenyl)phenoxy]ethyl]- acetate, (5) licarin C; benzofuran,2,3-dihydro-7

34 oil (0.5-2.0 mg); solvent, using acetone and ethyl acetate (6-12 ml); and surfactant concentration, u

35 rosophila melanogaster larvae in response to ethyl acetate (a volatile attractant) and carbon dioxide

36 In pure acetone and ethyl acetate, a linear friction-load relationship was o

37 its carbonyl compounds, namely acetaldehyde, ethyl acetate, acetic acid, and ketene, occurs on Au(111

38 azole) forms thermally stable complexes with ethyl acetate, acetic anhydride, N-methylsuccinimide, N-

39 Pentadecanal, ethyl acetate, acetoin, and ethanol may be potential pre

40 he target analytes chosen for the study were ethyl acetate, acetone, acetaldehyde, ethanol, ethylene

41 s: cyclohexane, toluene, 1,2-dichloroethane, ethyl acetate, acetone, acetonitrile, and THF.

42 common solvents, such as diethyl ether, THF, ethyl acetate, acetone, alcohol, acetonitrile, DMF, and

43 oxhlet extractor with five solvents: hexane, ethyl acetate, acetone, methanol, and methanol:water (80

44 gly more difficult in the order: chloroform, ethyl acetate acetonitrile, acetone, methanol, and aceti

45 fones in high yields with 10 mol % CrO(3) in ethyl acetate/acetonitrile at -35 degrees C.

46 The odourants included ethyl acetate, acetyl methyl carbinol, methylhexanoate,

47 indistinguishable from spectra obtained when ethyl acetate adsorbed directly onto the surface.

48 ious normal-phase chromatographic studies of ethyl acetate adsorption revealed nonlinear isotherms wh

49 h water and ethanol prior to extraction with ethyl acetate, all MK-7 will be made accessible prior to

50 evels of total phenols, sucrose, malic acid, ethyl acetate and 2-phenylethanol.

51 and concentration of fruity esters, such as ethyl acetate and 2-phenylethyl acetate.

52 was employed to the study the adsorption of ethyl acetate and 2-propanol to the surface of thin sili

53 Analytes were eluted using 20 mL of ethyl acetate and 5 mL of acetonitrile and finally the e

54 ules related to the VOO off-flavor (ethanol, ethyl acetate and acetic acid) was also shown.

55 the major volatiles excepting acetaldehyde, ethyl acetate and acetoine, whereas the application of o

56 ole with tritium, Pd/C, and triethylamine in ethyl acetate and afforded [(3)H]TDF with a specific act

57 ed on silica gel with a mixture of n-hexane, ethyl acetate and ammonia.

58 % NaCl), homogenised, filtered, extracted by ethyl acetate and analysed by liquid chromatography with

59 ontent (as 6OHLG equivalents) in methanolic, ethyl acetate and aqueous extracts from leaves of Cirsiu

60 Metabolites were extracted using ethyl acetate and assessed for antibacterial activity vi

61 Equilibrium effects showed synergy of ethyl acetate and benzaldehyde, favouring sorption of ad

62 tannins, exhibited the highest acetaldehyde, ethyl acetate and C6-compounds levels, and had increased

63 Notably, ethyl acetate and chloroform extracts displayed the high

64 Samples were extracted with ethyl acetate and cleaned up with primary secondary amin

65 d that involved a solvent extraction with an ethyl acetate and cyclohexane (50:50, v/v) mixture.

66 Using ethyl acetate and dichloromethane as shell- and core-pha

67 Extracts obtained with ethyl acetate and ethanol showed the promising antioxida

68 extraction using different solvents (hexane, ethyl acetate and ethanol).

69 e produced for ethanol, acetone, 2-butanone, ethyl acetate and eucalyptol, yielding R(2) > 0.99 and l

70 ethod based on liquid-liquid extraction into ethyl acetate and flow injection into the mass spectrome

71 The branch-ethyl acetate and fruit-methanol extracts exerted potent

72 vents was carried out using water, methanol, ethyl acetate and hexane in the presence/absence of form

73 Solubility in ethyl acetate and interaction with lipids, as determined

74 The ethyl acetate and methanol bark extracts of Melicope gla

75 The water-soluble ethyl acetate and methanol extraction methods were also

76 The ethyl acetate and methanol extracts from 16 Salvia L. sp

77 Ethyl acetate and methanol extracts of aerial parts harv

78 hibition and antioxidant activity of hexane, ethyl acetate and methanol extracts of Hedyotis biflora

79 hibition and antioxidant activity of hexane, ethyl acetate and methanol extracts of Hedyotis biflora

80 , two gamma-lactones, and one delta-lactone: ethyl acetate and methyl formate, beta-propiolactone, be

81 Human blood was extracted with ethyl acetate and methyl-t-butyl ether (2:98) under an a

82 he effect of treatment with petroleum ether, ethyl acetate and n-butanol extracts of rhubarb in a rat

83 hyl-1-butyl acetate, 2-phenylethanol, phenyl ethyl acetate and p-hydroxy phenyl ethanol.

84 Ethyl acetate and propyl acetate could be produced with

85 Pesticides were extracted with ethyl acetate and purified with gel permeation chromatog

86 r, but gamma-tocopherol content varied, with ethyl acetate and scCO2 + GLX recovering ~11 mug/100 g.

87 Maslinic acid was extracted from plasma with ethyl acetate and separated on a C18 column using a grad

88 tracted from M. xanthus cells with acidified ethyl acetate and sequentially purified by solid-phase e

89 Analysis shows that prolonged exposure to ethyl acetate and several related esters increases sensi

90 The extraction by ethyl acetate and subsequent electrochemical detection o

91 e and sulfatase, followed by extraction with ethyl acetate and subsequent separation by reversed-phas

92 id extraction and a mixture of acetonitrile, ethyl acetate and water, with preconcentration and deriv

93 e extracted from rat hepatic microsomes with ethyl acetate and were determined by HPLC using positive

94 lymer film consistent with poly(methylene-co-ethyl acetate) and subsequently hydrolyzing the ester si

95 Moreover, isopentyl acetate, ethyl acetate, and 2-phenethyl acetate were significantl

96 eriod, the medium was solvent extracted with ethyl acetate, and androgen metabolites were separated b

97 Dioxane, ethyl acetate, and beta-chloroethyl ether form relativel

98 rmed using petroleum ether, dichloromethane, ethyl acetate, and distilled water.

99 of three chemical flavorants (hexyl acetate, ethyl acetate, and methylbutyl acetate) that are found i

100 e of each fraction (hexane, dichloromethane, ethyl acetate, and n-butanol) was investigated.

101 Ethanol, ethyl acetate, and scCO2 + GLX showed the highest oil yi

102 ymatic reaction, quercetin is extracted with ethyl acetate, and subsequently oxidized under basic con

103 vials, overlaid with organic solvent such as ethyl acetate, and subsequently vortexed to extract hydr

104 , the fatty acyl ethyl ester (FAEE) analogue ethyl acetate, and the novel hCE1 inhibitor benzil.

105 number could produce significant amounts of ethyl acetate, arabinitol, glycerol and acetate in addit

106 t solvents (CS2, toluene, acetone, n-hexane, ethyl acetate) are extensively studied as well the PAE r

107 l organic solvents (e.g., methanol, ethanol, ethyl acetate) are widely used for extraction, reaction,

108 o different extraction procedures, employing ethyl acetate as a solvent, were useful in obtaining ext

109 The reaction is carried out in ethyl acetate as a solvent.

110 d support, 20 mg activated charcoal and 5 mL ethyl acetate as elution solvent.

111 rtificial cerebral spinal fluid (aCSF) using ethyl acetate as the extraction phase.

112 on is achieved by normal-phase HPLC with wet ethyl acetate as the mobile phase.

113 Infrared spectra of ethyl acetate at the silica surface versus concentration

114 and cymoxanil in grape and raisin matrix by ethyl acetate based extraction and liquid chromatography

115 s tert-butyl methyl ether, dioxane, anisole, ethyl acetate, beta-chloroethyl ether, and monoglyme, we

116 lysis decreased for most esters (75-fold for ethyl acetate) but not for methyl esters.

117 ile compounds, with increment in ethanol and ethyl acetate, but far below the odour threshold.

118 detecting high (1%-0.01%) concentrations of ethyl acetate, but some had deficits in detecting lower

119 g (acetate) L(-1) h(-1) in the first hour to ethyl acetate by the addition of excess ethanol and heat

120 Ethyl acetate can be defined a green and bio-based solve

121 , seven solvents-acetone, methanol, ethanol, ethyl acetate, chloroform, water, and hexane-were used t

122 stigated by applying native-Lugol and formol ethyl acetate concentration to stool specimens, and tric

123 1.5) increased the acetaldehyde, ethanol and ethyl acetate concentration, regardless of the fruit mat

124 n capture mass spectrometry when 1 microL of ethyl acetate containing essentially 20 amol of each pro

125 gth, methanol content, acetaldehyde content, ethyl acetate content and higher alcohols content were e

126 Ethyl acetate could also displace 2-propanol from the si

127 The fenugreek ethyl acetate crude extract (FGE3) demonstrated the high

128 Its ethyl acetate crude extract showed moderate antibacteria

129 in water; B, ammonium hydroxide in water; C, ethyl acetate; D, methanol: water (1:1, v/v); and E, ace

130 the delta(13)C(VPDB ethanol)-delta(13)C(VPDB ethyl acetate)-delta(13)C(VPDB isoamyl alcohol), delta(1

131 (13)C(VPDB isoamyl alcohol), delta(13)C(VPDB ethyl acetate)-delta(13)C(VPDB isoamyl alcohol)-delta(13

132 ta(13)C(VPDB n-propanol) and delta(13)C(VPDB ethyl acetate)-delta(13)C(VPDB n-propanol)-delta(13)C(VP

133 rifluoroacetic acid, methylene chloride, and ethyl acetate demonstrated that solvation differences ca

134 s, with increased citronellol, acetaldehyde, ethyl acetate, dicarboxylic acids esters, benzenoids, fu

135 using four different anti-solvents: toluene, ethyl acetate, diethyl ether, and chlorobenzene.

136 stable to silica gel chromatography (hexanes/ethyl acetate), dilute triethylamine in THF, and potassi

137 , dodecane, nonanoic acid, 2-(2-butoxyethoxy)ethyl acetate, (E)-2-undecanal and (S)-germacrene D, wer

138 hyl to the dansyl was observed in 2:1 hexane/ethyl acetate (EA) containing a few percent of methanol.

139 The ethyl acetate (EA) extract of Tripterygium wilfordii Hoo

140 ethanol/chloroform (T2) extract of TWHF, the ethyl acetate (EA) extract of TWHF, a purified diterpeno

141 Our results showed that ethyl acetate (EA) extract of WBM fruit in vitro potentl

142 namely water, ethanol, ethylene glycol (EG), ethyl acetate (EA), isopropanol (IPA), propylene glycol

143 CKD treated with the petroleum ether (PE)-, ethyl acetate (EA)- and n-butanol (BU)- extracts of rhub

144 romethane (DCM) as a diluent in concentrated ethyl acetate (EA)-based electrolyte, the co-solvent ele

145 d purified by a sodium hydroxide wash of the ethyl acetate eluting solvent and solid-phase extraction

146 equires a combined elution with methanol and ethyl acetate, especially for increasing the recovery of

147 extraction using gamma-valerolactone (GVL), ethyl acetate (EtAc), and cyclopentyl methyl ether (CPME

148 ntary impact of solvents (acetonitrile, ACN; ethyl acetate, ETAC; pyridine, PYR) and catalysts (trime

149 Ethyl acetate, ethanol, isopropanol, n-heptane and cyclo

150 Extractions were performed with ethyl acetate, ethanol, water and ethanol:water to devel

151 The odorants were ethyl acetate, ethyl butyrate, isoamyl acetate, and isoa

152 hylbutan-1-ol, 1-pentanol, octanal, nonanal, ethyl acetate, ethyl octanoate, and butane-2,3-dione) re

153 ormed stereospecifically from Ti(O-i-Pr)(4), ethyl acetate, EtMgBr, and trans-beta-deuterostyrene.

154 nts: acetonitrile (AcCN), n-butanol (nBuOH), ethyl acetate (EtOAc), isopropanol (iPrOH), and tetrahyd

155 and compare the biological activities of the ethyl acetate (EtOAc), methanolic (MeOH) and aqueous ext

156 Notably, films made with ethyl acetate exhibited superior stability compared to o

157 sis discovered 40 bioactive compounds in the ethyl acetate extract (ECDF).

158 An ethanol/ethyl acetate extract from the roots of TWHF was prepare

159 y was higher in butanol extract, whereas the ethyl acetate extract had the highest inhibitory effect

160 ogenic microbes, have been isolated from the ethyl acetate extract of B. amyloliquefaciens.

161 Ethyl acetate extract of peel reduced expression of indu

162 These results showed that the ethyl acetate extract of the fenugreek seeds had a signi

163 The ethanol/ethyl acetate extract of TWHF shows therapeutic benefit

164 Only the fruit-ethyl acetate extract quenched SO radical (38.4 +/- 1.01

165 Only the ethyl acetate extract reduced total cholesterol, triglyc

166 The nephroprotective effect of ethyl acetate extract was better than other extracts.

167 gnificantly after oral administration of the ethyl acetate extract, compared with those of HCD-fed ra

168 nt and total flavonoid content were found in ethyl acetate extract, methanol extract possessed the st

169 s were o-phenylenediamine (OPD) derivatized, ethyl acetate extracted, lyophilized in a vacuum centrif

170 ing five metabolites) in passion fruit using ethyl acetate extraction and dispersive solid-phase extr

171 ing five metabolites) in passion fruit using ethyl acetate extraction and dispersive solid-phase extr

172 Ethyl acetate extraction and LC-MS/MS analysis were used

173 For isolation of CPs from fish, an ethyl acetate extraction followed by a clean-up of the e

174 Assay of serum curcumin by ethyl acetate extraction followed by liquid chromatograp

175 ant with that determined via the traditional ethyl acetate extraction procedure.

176 Ethyl acetate extraction was also found to reduce interf

177 trix solid phase dispersion and a dispersive ethyl acetate extraction were compared.

178 Using a combination of ethyl acetate extraction, reversed-phase C(18) chromatog

179 al techniques, such as QuEChERS and buffered ethyl acetate extraction, this method provided superior

180 with phenyl boronic acid (PBAc) followed by ethyl-acetate extraction.

181 ollowed by equilibration and solid-phase and ethyl acetate extractions to prepare samples for liquid

182 the most abundant compounds in methanol and ethyl acetate extracts (ME and EAE), respectively.

183 Ethanol extracts of AB (ABE) and ethyl acetate extracts AB (ABEa) were obtained and furth

184 Both ethanol and ethyl acetate extracts in peel and pulp decreased produc

185 s(III)-unexposed, early-log-phase cells with ethyl acetate extracts of As(III)-unexposed, late-log-ph

186 t the transcriptional level was activated by ethyl acetate extracts of culture supernatants or by syn

187 ived lipid radicals were measured ex situ in ethyl acetate extracts of model systems and extrudates b

188 Both ethyl acetate extracts of peel and pulp mitigated expres

189 t amounts in aqueous extract of peel, but in ethyl acetate extracts of peel, oleanolic acid, caroteno

190 Interestingly, CFS and crude ethyl acetate extracts of PUFSTP35 (Bacillus licheniform

191 s (bcAR) and methylalkylresorcinols (mAR) in ethyl acetate extracts of quinoa.

192 The hexane and ethyl acetate extracts of strawberry guavas showed cyclo

193 liquid chromatography of highly concentrated ethyl acetate extracts revealed that culture supernatant

194 ontents were highest in the methanol and the ethyl acetate extracts.

195 showed potent effect compared to hexane and ethyl acetate extracts.

196 rison involved liquid-liquid extraction into ethyl acetate followed by LC-ESI-MS/MS and acetonitrile

197 Soil microcosms were extracted with ethyl acetate followed by two heated 90/10 v/v acetonitr

198 ) involving a double solvent extraction with ethyl acetate, followed by a clean-up step with florisil

199 Pesticides are extracted from raisins with ethyl acetate, followed by centrifugation.

200 s, based on pressurized liquid extraction by ethyl acetate, followed by selective identification and

201 raction of the desired products using DCM or ethyl acetate, followed by subjecting the recovered aque

202 -phase extraction on silica cartridges using ethyl acetate for application of the sample and an ethyl

203 dation of ethanol are 1,1-diethoxyethane and ethyl acetate formed from condensation of acetaldehyde o

204 Methylene chloride/ethyl acetate/formic acid (6:10:1, v/v) as the mobile ph

205 The major active compounds found in the ethyl acetate fraction are unsaturated fatty acids such

206 The ethyl acetate fraction displayed the highest antioxidant

207 The ethyl acetate fraction exhibited inhibitory activity aga

208 The ethyl acetate fraction inhibited in vitro alpha-glucosid

209 This study was designed to investigate ethyl acetate fraction of Chinese olive fruit extract (C

210 armelin) was isolated and characterized from ethyl acetate fraction of extracts of Aegle marmelos.

211 The ethyl acetate fraction of red seaweed Hypnea musciformis

212 oglucinol Equivalence/g in the semi-purified ethyl acetate fraction while the NMR spectrum and the LC

213 nalysis were used to identify the bio-active ethyl acetate fraction.

214 P. guajava was partitioned into aqueous and ethyl acetate fractions and studied for its antibacteria

215 Effects of I. fumosorosea and cell-free ethyl acetate fractions derived from the fungus on the B

216 The synergistic effect of ethyl acetate fractions of seaweeds Kappaphycus alvarezi

217 Isolated n-hexane, chloroform and ethyl acetate fractions suppressed fungal biomass by 32-

218 traction to enrich hydroxyl metabolites into ethyl acetate from an aqueous sample.

219 y the effect of pH on phenol extraction with ethyl acetate from the aqueous phase of hydrothermally t

220 tes; 2-propanol was shown to easily displace ethyl acetate from the silica surface.

221 yl propionate from hydroxyethyl acrylate and ethyl acetate from vinyl acetate, respectively.

222 the fungal mycelium as well as by cell-free ethyl acetate fungal extracts.

223 olvents such as acetonitrile/water (1:1) and ethyl acetate further enhanced sensitivity and reproduci

224 and K (the Avrami "rate constant") for CeNC/ethyl acetate gelation with those reported previously fo

225 one, acetonitrile, dichloromethane, ethanol, ethyl acetate, hexane, and toluene) on graphene.

226 vities of various extracts (water, methanol, ethyl acetate, hexane, dichloro-methane) of fenugreek se

227 lar solvents such as carbon tetrachloride or ethyl acetate/hexane and 2-5% of a polar solvent such as

228 and purified from rat brain tissue using an ethyl acetate/hexane solvent extraction, followed by a s

229 ative test cases: kinetics of acid-catalyzed ethyl acetate hydrolysis and amidization of surface-teth

230 L) showing the highest activity, followed by ethyl acetate (IC(50) = 473.87 +/- 1.4 ug/mL) and methan

231 w/v), 80 min of shaking and by adding 30% of ethyl acetate in acetone, being beta-carotene the major

232 Acetonitrile was superior to ethyl acetate in terms of selectivity, though they were

233 t systems demonstrated that the inclusion of ethyl acetate inverted the ratio of relative intensities

234 We demonstrate that ethyl acetate is able to extract octylglycoside from a p

235 ines to oximes using m-CPBA as an oxidant in ethyl acetate is described.

236 Ethyl acetate is used as the extraction solvent in place

237 ropanoate, ethyl butanoate, ethyl octanoate, ethyl acetate, isoamyl acetate, isobutanol, 2-methyl-1-b

238 ity (15), porphyrin 2 was first reacted with ethyl acetate/LDA and the intermediate alcohol 14 was th

239 omplex from a mixture of common alcohols and ethyl acetate led to the formation of an NHC-silver acet

240 ne-1-carbonyl)imino)benzo[d]thiazol-3(2H)-yl)ethyl acetate ligand (MRI-2646) acts as a partial agonis

241 with M. pulcherrima showed concentrations of ethyl acetate likely to affect negatively wine aroma.

242 ion of polymerization increases in the order ethyl acetate << methyl ethyl sulfone < acetonitrile < N

243 ction was performed with hexane, chloroform, ethyl acetate, methanol, and water.

244 Chemical investigation of ethyl acetate-methanol extract of the venerid bivalve cl

245 The quaternary solvent system n-heptane-ethyl acetate-methanol-water (6:5:6:5 v/v) was used in t

246 rizona solvent systems composed of n-heptane/ethyl acetate/methanol/water led to ten fractions.

247 acetate for application of the sample and an ethyl acetate:methanol (1:1) mixture for elution.

248 uantitatively extracted from cellulose by an ethyl acetate:methanol (1:1) mixture.

249 d from soda and Kraft alkaline lignins using ethyl acetate, methyl ethyl ketone (MEK), methanol and a

250 , two gamma-lactones, and one delta-lactone: ethyl acetate, methyl formate, beta-propiolactone, beta-

251 Samples were extracted with acidified ethyl acetate, MgSO4 and CH3COONa and cleaned up by disp

252 olar solvents (e.g., hexane/ethyl acetate or ethyl acetate) mixed with a small amount of a polar solv

253 GF(2alpha) isomers from solution in a hexane:ethyl acetate mixture (10:1) on a cellulose support prep

254 shing of the cellulose squares by the hexane:ethyl acetate mixture (10:1), fluorescent derivatives of

255 ere extracted from the sample by cyclohexane-ethyl acetate mixture (1:1 v/v) and cleaned up by floros

256 nyldiazomethane dissolved in the same hexane:ethyl acetate mixture.

257 sing various solvents, including chloroform, ethyl acetate, n-hexane, methanol, and water.

258 e, a significant increase in acetic acid and ethyl acetate occurred, while at 10 degrees C their valu

259 quid mixtures consisting of a polar solvent (ethyl acetate or acetone) in heptane.

260 genic comminution, extraction with acidified ethyl acetate or acetonitrile, and dilution of the final

261 nes upon treatment with a lithium enolate of ethyl acetate or alpha-substituted acetates.

262 discriminating low concentrations of either ethyl acetate or butanol from non-odorized air.

263 In nonpolar solvents (e.g., hexane/ethyl acetate or ethyl acetate) mixed with a small amoun

264 and 4 in the presence of methanol, ethanol, ethyl acetate, or water.

265 capacities of the crude extract, aqueous and ethyl acetate partitions of Limoniastrum guyonianum Bois

266 ere identified on the main column as peak 1, ethyl acetate; peak 2, a mixture of octanol and ethyl pr

267 The ethyl acetate phase exhibited a significant antioxidant

268 , at 450 and 600 degrees C, from TiCl(4) and ethyl-acetate precursors.

269 The low-temperature formation of the ester, ethyl acetate, proceeds via the coupling of acetaldehyde

270 preparation method involving extraction with ethyl acetate provided 80-107% recoveries for both the p

271 mic hydrolysis of the urine, extraction with ethyl acetate, radioimmunoassay, and separation of free

272 robic metabolites (acetaldehyde, ethanol and ethyl acetate), regardless of storage temperature and ti

273 Acetoin (or ethyl acetate) represented a significant pork quality ma

274 Bioassay-guided fractionation of the active ethyl acetate soluble fraction has led to the isolation

275 The ethyl acetate soluble fraction obtained from the hot wat

276 en heated with endo-bornyltriazolinedione in ethyl acetate solution, conversion to a 1:1 mixture of 3

277 A limit of precise isotope analysis for ethyl acetate solutions of 10 mg/L atrazine, 10 mg/L ace

278 liquid-liquid extraction using a hexane and ethyl acetate solvent system.

279 ction with LiOH, NaOH, and NMe(4)OH and with ethyl acetate substrate reveals that the temperature of

280 ly, the change of solvent from chloroform to ethyl acetate switches the membrane property from hydrop

281 revealed two-adsorbed-component spectra for ethyl acetate that were indistinguishable from spectra o

282 gh the 1,2 addition of the cerium enolate of ethyl acetate to 2,6,6-trimethylcylohexenone.

283 ining phenolic compounds, was extracted with ethyl acetate to obtain flavonoids which were separated

284 s of some solvents (water, ethanol, acetone, ethyl acetate), used as pure or in binary and ternary mi

285 ation (%P13C ) of ca. 1.8 % were achieved in ethyl acetate utilizing 50 % para-hydrogen corresponding

286 ological disorders, and the concentration of ethyl acetate was below the odour threshold.

287 Ethyl acetate was used to extract these phenolic compoun

288 n the aqueous fraction after extraction with ethyl acetate were identified.

289 ong tested aroma compounds, benzaldehyde and ethyl acetate were most sorbed and preferentially into t

290 compounds, amyl alcohols, ethyl lactate and ethyl acetate were quantitatively relevant in all of the

291 adhesion forces measured in pure acetone and ethyl acetate were small (0.24 nN) but increased logarit

292 Racemic VAPOL and solvates with toluene and ethyl acetate were structurally characterized.

293 gents (H(2)O(2) in isopropyl alcohol, ODI in ethyl acetate) were injected in a test tube or strip-wel

294 that only two variables (ethyl decanoate and ethyl acetate) were necessary for a successful different

295 m lipoyl-N-epsilon-lysine by extraction into ethyl acetate where it can react with DBQC.

296 litude electroantennogram (EAG) responses to ethyl acetate, whereas Gprk2 mutants produce constant lo

297 s observed for 2-methylpropanal, hexanal and ethyl acetate while the highest interaction was observed

298 Solid samples were extracted with ethyl acetate, while liquid samples were directly inject

299 2.5), as was the rate of the condensation of ethyl acetate with aminoethanol (k(vis/UV) = 100).

300 ction, and in particular the methanolysis of ethyl acetate with sulfuric acid as catalyst, is used as