ライフサイエンスコーパス: methanol

1 , ethylene glycol, acetaldehyde, ethane, and methanol).

2 terification of 1-octanol at 60 degrees C in methanol.

3 that yield noncompetitive substrates such as methanol.

4 e, followed by a final hydrogenation to give methanol.

5 l molecular weight organic dyes dissolved in methanol.

6 ce of water or other protic solvents such as methanol.

7 e fluids including refrigerants (R245Fa) and methanol.

8 to that of the intrinsic nanoMIL-101(Cr) in methanol.

9 me subsequent selective hydrogenation toward methanol.

10 ons from boiling vegetables are dominated by methanol.

11 and reagents, moreover, avoiding the use of methanol.

12 methane rapidly at room temperature to form methanol.

13 trameric aggregate in the solid state and in methanol.

14 rt on the use of water to oxidize methane to methanol.

15 trimethylamine and to H-bond donors such as methanol.

16 ting/bridging ligand alpha-methyl-2-pyridine-methanol.

17 e the primary reaction mechanisms leading to methanol.

18 ar patterns, such as oligogalacturonides and methanol.

19 enabling its selective partial oxidation to methanol.

20 ial was cryo-milled and extracted with water/methanol.

21 ss and the residue reconstituted in 50muL of methanol, 1muL of which was injected into the GC-MS.

22 using a mobile phase containing acetonitrile:methanol:2-propanol in the ratio of 85:15:33 with 0.01%

23 he best conditions were extraction with 100% methanol (2mM NaF) during 30min for table olives, and 91

24 NaF) during 30min for table olives, and 91% methanol (2mM NaF) during 40min for olive paste.

25 es were dissolved in acetone-dichloromethane-methanol (3:2:1, v/v/v) and diluted with acetonitrile-me

26 Small quantities of water or methanol (5-10 wt %), which effectively mobilized all co

27 0, diethyl ether: 2.80, ethyl acetate: 4.40, methanol: 5.10 and water: 9.0D) were selected for optimi

28 he association in deuterated benzene/acetone/methanol 70:30:1 at 283 K reaches Ka =(2.11+/-0.39)x10(5

29 achieved on a C18 column with 2% acetic acid/methanol (96:4, v/v) as the mobile phase.

30 amics to study the microscopic properties of methanol, a prototypical HB liquid.

31 when the same titration was repeated in pure methanol, a solvent in which the sensor does not aggrega

32 present the use of a heptane cosolvent in a methanol acceptor phase in combination with a polydimeth

33 .5x using 0.046 mole fraction heptane in the methanol acceptor.

34 d for predicting the alcoholic strength, the methanol, acetaldehyde and fusel alcohols content of gra

35 sses for the direct conversion of methane to methanol, acetic acid and other useful chemicals.

36 ined sulfadiazine was eluted using 180muL of methanol/acetic acid (6:4) and quantified by fiber optic

37 our solvents varying from polar to nonpolar (methanol, acetone, dichloromethane, and n-hexane) were s

38 s using mobile phase consisted of chloroform:methanol:acetone:25% ammonium hydroxide (75:15:10:1.6 v/

39 other compounds was performed using C18 and methanol-acetonitrile with gradient elution system.

40 led to an increase in the amounts of aqueous methanol-acetonitrile-soluble apiose but did not result

41 uenching/extraction techniques (such as cold methanol/acetonitrile/water, hot water, and boiling etha

42 omenex Synergi 4mu Hydro-RP 80A column using methanol: acetonitrile (ACN): 0.1% phosphoric acid (60:1

43 consisting of 10mM aqueous ammonium acetate:methanol:acetonitrile (50:30:20; v/v/v) with detection a

44 column using mobile phase consisting of (A) methanol:acetonitrile (8:2) - (B) 0.1% formic acid in a

45 use it poses health risks e.g. from possible methanol admixture.

46 pounds by use of hydrochloric acid (12 N) in methanol afforded the desired free amino acids in 80-88%

47 orce measurements in aqueous solution versus methanol allowed quantification of the hydrophobic inter

48 cally favorable outcome is the production of methanol along a pathway involving the sequential hydrog

49 anyl]-2,6-d imethoxy, (4) 1,3-benzodioxate-5-methanol,alpha-[1-[2,6-dimethoxy-4-(2-propenyl)phenoxy]e

50 s [methanol/sodium hydroxide (MeOH/NaOH) and methanol/ammonium hydroxide (MeOH/NH4OH)].

51 e from catalytic dehydrogenative coupling of methanol and 1,2-diamine is demonstrated.

52 le pretreatment consisted of extraction with methanol and a homogenising step (cooked ham, minced mea

53 p may be oxidized in situ in the presence of methanol and a hypervalent iodine reagent to form an act

54 catalyse the direct conversion of methane to methanol and acetic acid, using oxygen and carbon monoxi

55 identified and determined quantitatively in methanol and acetone extracts from quince peel and pulp,

56 t synthesis of dimethyl carbonate (DMC) from methanol and carbon dioxide.

57 ogen evolution reaction, electrooxidation of methanol and CO, and electroreduction of CO2.

58 sess economical aspects of the production of methanol and DME and outline future research and develop

59 ria-zirconia (NiO/CZ) can convert methane to methanol and ethanol in a single, steady-state process a

60 e most active molecular electrocatalysts for methanol and ethanol oxidation.

61 lagitannins requires a combined elution with methanol and ethyl acetate, especially for increasing th

62 entally for the first time the production of methanol and formaldehyde from CO hydrogenation on Ni(11

63 biguous answer to the eventual production of methanol and formate, much more so than (13)C NMR, which

64 se the reaction of CH4 and water to generate methanol and H2 is highly unfavorable at any temperature

65 Microwave power, methanol and HCl concentration significantly (p<0.05) af

66 Formation of methanol and hydrocarbon derivatives from CO2 and H2, th

67 of CO and H2 , is a key feedstock to produce methanol and liquid fuels in industry, yet limited succe

68 While traditionally mainly methanol and long-chain hydrocarbons are produced by CO

69 as achieved by solid-liquid extraction using methanol and methyl tert-butyl ether.

70 good yields (90% and >95% respectively, with methanol and N,N'-dimethylethylenediamine as dehydrogena

71 of catalytic conversion of methane to liquid methanol and other oxygenates would be of considerable p

72 nzene selectively at low temperature to form methanol and phenol, respectively.

73 pounds were extracted with 80% (v/v) aqueous methanol and purified by liquid chromatography.

74 round electrolyte, BGE (borax, acetonitrile, methanol and SDS concentrations), was studied and optimi

75 uently found in surface water were spiked in methanol and surface water extracts at two different con

76 of polystyrene nanospheres (300 nm), water, methanol and surfactant in the solution, crucial for lar

77 Analytes were extracted with methanol and the extracts cleaned-up by solid-phase extr

78 Finally, liposomes are ruptured by methanol and the released-dopamine is subsequently measu

79 the hydrogenation of CO2 to formic acid and methanol and the reverse dehydrogenation reactions.

80 The extraction was performed in methanol and then analyzed by gas chromatography-mass sp

81 num and alpha-MoC act in synergy to activate methanol and then to reform it.

82 These mitochondria are extracted with methanol and water.

83 lective absorptive and emissive responses to methanol and water.

84 acted with two organic solvents (ethanol and methanol) and characterized for phenolic composition, an

85 nit is deliberately chosen to host pyridine, methanol, and ammonia as guest molecules.

86 hydrogenation of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly reviewed, wi

87 on (SPE), methylated by boron trifluoride in methanol, and injected into GC-FID system.

88 ntial of +0.97 V, excellent tolerance toward methanol, and long-term stability.

89 d of the Coomassie Brilliant Blue G-250 dye, methanol, and phosphoric acid, has been traditionally us

90 alkynes, chiral (S)-diphenyl(pyrrolidin-2-yl)methanol, and propiolates gave the corresponding chiral

91 tions has been on aqueous-phase reforming of methanol (APRM).

92 ction mechanisms leading both to methane and methanol are considered.

93 At very cathodic potentials, formic acid and methanol are formed as well.

94 ion of N2O by Paracoccus denitrificans using methanol as a carbon/electron source.

95 anotrophic organisms with the ability to use methanol as an energy source.

96 l as in the competition mode using ferrocene methanol as redox mediator.

97 ine-3-dimethyl acetal at room temperature in methanol as solvent.

98 induction phase for product expression using methanol as the inducer.

99 ins, besides hydrogen and water, methane and methanol as the most abundant species.

100 tions are highly atom-efficient and generate methanol as the only byproduct.

101 s of photoelectrochemical (PEC) oxidation of methanol, as a model organic substrate, on alpha-Fe2O3 p

102 scuss the thermal decomposition of water and methanol, as well as the reactions of CO and CO2 over TM

103 100 degrees C methanol ASE extract exhibited the highest antiradical a

104 ple preparation method, including the use of methanol at a 3:1 ratio of solvent to milk for protein p

105 Fundamental aspects of the dynamics of methanol at room temperature were contextualised only ve

106 aluminum oxide, which shows the formation of methanol at the interface and the effect of water molecu

107 : pH 9.5, 0.14 M Britton Robinson buffer and methanol between 5% and 10%.

108 ntres, which are tolerant to carbon monoxide/methanol, but highly active for the oxygen reduction rea

109 residue types support 12-helical folding in methanol, but only the cyclically constrained gamma resi

110 are hydrogenated back to the free amine and methanol by a simple hydrogen pressure swing.

111 Insertion of 2-substituted dienes into the methanol C-H bond occurs in a regioselective manner to f

112 low production yields (100 t/y) compared to methanol carbonylation (0.26 pound/kg, 261 pound/t) and

113 eforming, methanol synthesis, and subsequent methanol carbonylation on homogeneous catalysts.

114 are extracted using a biphasic method, with methanol, chloroform and water as the solvents.

115 compared polyphosphate extraction in water, methanol-chloroform, and phenol-chloroform followed by p

116 erol oxidase (ChOx), a member of the glucose-methanol-choline (GMC) family, catalyzes the oxidation o

117 of differential distortion of the anhydride-methanol complex in the transition state as the factor l

118 Several extraction variables, including methanol composition (50-100%), temperature (10-70 degre

119 well-known Scotch whisky brands, and detect methanol concentrations well below the maximum human tol

120 gineered enzyme assembly improved whole-cell methanol consumption rate by ninefold.

121 To increase methanol consumption, an "NADH Sink" was created using E

122 urcuminoids increased at lower pH and higher methanol content and decreased in the opposite vertex of

123 ol-water mixtures (between 30 and 70% v/v of methanol content) on the stability of curcumin and its a

124 atalytic process for converting methane into methanol could have far-reaching economic implications.

125 hat the reaction intermediates produced from methanol decomposition are poised to directly undergo hy

126 ethanotroph, gene expression of the dominant methanol dehydrogenase (MDH) shifts from the lanthanide-

127 trophs, being co-factors in the XoxF type of methanol dehydrogenase (MDH).

128 for low-temperature (<100 degrees C) aqueous methanol dehydrogenation to H2 and CO2.

129 rroborate a Curtin-Hammett scenario in which methanol dehydrogenation triggers rapid, reversible dien

130 (unlike steam reforming) or CO (by complete methanol dehydrogenation).

131 lly be detected, e.g., an LOD of 2.5 ppm for methanol detection was acquired.

132 While for methanol detection, we track the -OH absorption at lambd

133 itial reactivity studies of 2 toward CO2 and methanol, different isomerization pathways depending on

134 The products, methanol, dimethyl ether, and CO2, were desorbed with th

135 clean and storable fuel (e.g., hydrogen and methanol) directly from sunlight, water and CO2.

136 nd operating cost, proved to be: 40% ethanol:methanol during 40min, under 40 degrees C, and 100bar.

137 cific activity over commercial catalysts for methanol electrooxidation after 10,000 cycles.

138 They were subsequently exploited for methanol electrooxidation in alkaline media.

139 onally activated dissociation (CAD) of these methanol-eliminated adduct ions (MS(3) experiments) prod

140 Methanol elimination is predicted to be the turnover-lim

141 5, and 123 for sulfones, while an additional methanol elimination was observed for carboxylic acids a

142 nucleophilic addition; and solvent-assisted methanol elimination.

143 quid fuels and chemicals (e.g., acetic acid, methanol, ethanol, and formaldehyde) were synthesized in

144 eactions for fuel cells (electrooxidation of methanol, ethanol, and formic acid).

145 )-O2)] reacts at low temperature with H2O in methanol/ether solution to form trans-[Pd(IPr)2(OH)(OOH)

146 Derivatives of (2-methyl-3-biphenylyl)methanol exhibit the structures capped on one side of th

147 MIL-101(Cr)/GO in methanol exhibited a significant increase in the thermal

148 Puree of both species and methanol extract of air-dried R. canina hips showed some

149 The methanol extract of Laminaria digitata and the acetone e

150 precursor, compound 2 were isolated from the methanol extract of the trunks of Abies holophylla.

151 Chemical investigation of ethyl acetate-methanol extract of the venerid bivalve clam Paphia mala

152 HPLC/MS analysis of the methanol extract showed the presence of ellagic acid (EA

153 In this work, the light absorption of methanol-extractable OC from prescribed and laboratory B

154 The method comprises methanol extraction followed by HPLC-MS analysis, and wa

155 Methanol extraction gave the highest yields for all clas

156 The light absorption of methanol extracts showed a strong wavelength dependence

157 ations of studied compounds were detected in methanol extracts, after 12h incubation of the samples a

158 city and signal-to-background ratio by using methanol fixation and inclined laser illumination.

159 f methanotroph MDHs, resulting in release of methanol for its growth.

160 The present study confirms the lack of methanol formation upon bulk electrolysis of PyH(+) solu

161 ine (PyH(+)) could catalyze the formation of methanol from the reduction of CO2 on a platinum electro

162 ase boundary (TPB) layer of a passive direct methanol fuel cell (DMFC) as biosensor transducer is her

163 highly efficient cathode materials in direct methanol fuel cells (DMFCs).

164 ng the DNA@ZIF-8 hybrid membrane into direct methanol fuel cells, it exhibits a power density of 9.87

165 proton-conductivity membrane used for direct methanol fuel cells, providing bright promise for such h

166 Similarly, the oxidation of methanol generates formaldehyde and formic acid which th

167 loidal TiO2 nanoparticles in the presence of methanol gives highly reduced suspensions.

168 catalytic enantioselective C-C couplings of methanol (>30 x 10(6) tons/year) are reported.

169 tions, the dried fruit sample mixed with 80% methanol having 3.0 pH in a ratio of 1:50 and the mixtur

170 er-4 (GLUT4) in the anti-diabetic effects of methanol, hexane and dichloromethane extracts of the aer

171 In the absence of methanol, hydrogen transfer occurs between olefins and n

172 Innovative methods to detect methanol in alcoholic beverages are being constantly dev

173 metry was achieved by using lesser levels of methanol in both initial and final gradient elution (-1.

174 ediate the facile conversion of methane into methanol in methanotrophic bacteria with high efficiency

175 ng step can be termed as "amine reforming of methanol" in analogy to the traditional steam reforming.

176 e (H2O2), we demonstrated that the resulting methanol incorporated a substantial fraction (70%) of ga

177 dihydro-1,4-benzodioxin-6-yl)-2-methylphenyl]methanol induce an enlarged interaction interface that r

178 Exposure to methanol induces a similarly-rapid and reversible colour

179 handed 10/12-helix, while the CD spectrum in methanol inferred a right-handed secondary structure.

180 Methanol is a poison which is frequently discovered in a

181 Methanol is an important feedstock derived from natural

182 y demonstrates that the dynamic behaviour of methanol is much richer than what so far known, and prom

183 Methanol is oxidized on alpha-Fe2O3 to formaldehyde with

184 and catalytically generate products such as methanol is particularly attractive.

185 Among those, methanol is particularly important (because of its toxic

186 The use of methanol is particularly interesting in this regard, bec

187 and Bronsted acid sites dominates as long as methanol is present in the reacting mixture, leading to

188 Further investigations revealed that no methanol is produced.

189 Correspondingly, methanol is released into the medium only when the metha

190 on profiles and mutant analyses suggest that methanol is the dominant carbon and energy source the me

191 oion coincidence measurements carried out on methanol isotopomers, ethylene glycol, and acetone.

192 tify the key intermediates where branches to methanol, ketene, ethanol, acetylene, and ethane are kin

193 (H3BTTri) in N,N-dimethylformamide (DMF) and methanol leads to the formation of Co-BTTri (Co3[(Co4Cl)

194 tivity at the omegaB97X-D/Def2-TZVPPD/SCRF = methanol level revealed that in addition to direction re

195 fectively reductively couples NO(g) at RT in methanol (MeOH), giving a structurally characterized hyp

196 multaneous measurement of isoprene, ethanol, methanol, methane, and water.

197 fusion but was less potent, and low doses of methanol mildly inhibited fusion.

198 ty formed diagnostic adducts that had lost a methanol molecule upon reactions with TMMS.

199 found to be incompressible when filled with methanol molecules within a diamond anvil cell.

200 non-polar organic liquids (acetone, ethanol, methanol, N-methyl-2-pyrrolidone (NMP), carbon tetrachlo

201 The response plots revealed that addition of methanol noticeably improved the stability of curcuminoi

202 at electrocatalytic oxidation of ethanol and methanol occurs via two- and four-electron oxidation pro

203 , giving a carbon selectivity for methane to methanol of 45-60%.

204 cinnamon stars and buns were extracted with methanol only.

205 i(II)2(mu-X)3]X (X = Cl or Br) with NaOCl in methanol or acetonitrile (where L = 1,4,7-trimethyl-1,4,

206 The highest flavanol content using either methanol or ethanol was determined in the green chicory

207 with solvents of different polarity (water, methanol or ethanol).

208 These organisms were mainly enriched with methanol or formate.

209 r this reaction, suggesting a minor yield of methanol or stabilized trioxide as a product.

210 node methoxy (or ethoxy) groups formed from methanol (or ethanol).

211 s gold for amplified electrocatalysis toward methanol oxidation and oxygen reduction reactions.

212 s under quasi-steady-state conditions of PEC methanol oxidation indicates that rate of reaction is se

213 studies determine that the rate constant for methanol oxidation on alpha-Fe2O3 is retarded approximat

214 Catalysts for methanol oxidation reaction (MOR) are at the heart of ke

215 in both acidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZ

216 scuss the implications for the efficient PEC methanol oxidation to formaldehyde and concomitant hydro

217 oying these data, we propose a mechanism for methanol oxidation under 1 sun irradiation on these meta

218 s indicate similar second-order kinetics for methanol oxidation with a second-order rate constant 2 o

219 ch as hydrocarbon oxidation, electrochemical methanol oxidation, and hydrogen fuel cells.

220 ter-sphere redox probe, reversible ferrocene methanol oxidation.

221 and highest electrocatalytic activity toward methanol oxidation.

222 ram of catalyst, or around 230 micromoles of methanol per gram of catalyst, respectively, with select

223 side the cavities of the ZIF-8, but very low methanol permeability of 1.25 x 10(-8) cm(2) s(-1) due t

224 potassium hydrogen phthalate (KHP) in 1% v/v methanol (pH 5.5) and 20mmolL(-1) EDTA, 2mmolL(-1) KHP,

225 olL(-1) KHP, 40mmolL(-1) (NH4)2CO3 in 1% v/v methanol (pH 9.0) formed mobile phase B.

226 need to mix CO into the industrial feed for methanol production from CO2, as it scavenges the chemis

227 alculations suggest that the reaction toward methanol production is highly favorable compared to form

228 material composition, we are able to reach a methanol productivity as high as 0.2 mol CH3OH/mol Cu (1

229 the reducibility of the materials and their methanol productivity.

230 increase axon conduction, 4-aminopyridine-3-methanol, promotes further improvement in CST-dependent

231 imilar inhibitory effects were observed with methanol, propanol, and butanol, with ethanol being the

232 g a wide range of potential applications for methanol quantification.

233 actional distillation presented a decreasing methanol ratio (from 4% to <0.5%) and a growing ethanol

234 ochemical reduction of CO2 to formate and to methanol remains an open question.

235 ts of the methane oxidation pathway, such as methanol, represent alternative carbon sources.

236 ) were obtained for ethanol, n-propanol, and methanol, respectively.

237 er group, subsequent hydrolysis, and loss of methanol resulting in the formation of the ABLs.

238 ctivity of Rhas been investigated in aqueous methanol, resulting in fluorescence shift and selective

239 pid, transient extracellular accumulation of methanol, revealing a way in which methane-derived carbo

240 ce was evaluated for two extraction methods [methanol/sodium hydroxide (MeOH/NaOH) and methanol/ammon

241 inear correlation found between the logKa in methanol solution and the depth of (+)N-CH3 cavity inclu

242 Furthermore, slow evaporation of methanol solutions of 3 produced crystals whose structur

243 osition and concentration of the salt/acidic-methanol solutions.

244 ules were suspended in ion-containing acidic methanol solutions.

245 rapid and reversible colour change to a blue methanol solvate.

246 o, revealed an alpha-helical conformation in methanol, stabilized by an unusual (i,i+3) staple which

247 But traditional reforming of methanol steam operates at relatively high temperatures

248 nks to the mechanisms of Fischer-Tropsch and methanol syntheses.

249 based, modified Fischer-Tropsch and modified methanol synthesis catalysts.

250 Cu and ZnO at the interface that facilitates methanol synthesis via formate intermediates.

251 ly obtained through methane steam reforming, methanol synthesis, and subsequent methanol carbonylatio

252 ivity of ZnCu and ZnO/Cu model catalysts for methanol synthesis.

253 st precursors for the industrially important methanol-synthesis and low-temperature water-gas shift (

254 ptimized by a 3(2) factorial design (%HCl in methanol, temperature, and time) and response surface me

255 ts for carbon dioxide (CO2) hydrogenation to methanol, the Zn-Cu bimetallic sites or ZnO-Cu interfaci

256 acid-catalysed reactions, the dehydration of methanol to dimethyl ether and the total methane oxidati

257 odified by PhanePhos, CF3-allenes react with methanol to form branched products of hydrohydroxymethyl

258 yde and formic acid which then condense with methanol to form dimethoxymethane and methyl formate, re

259 s the major route in catalytic conversion of methanol to olefins (MTO) for the formation of nonolefin

260 carboxylic acid), ranging in complexity from methanol to plant hormones (gibberellins, containing eig

261 QDs in the electrolyte was also improved by methanol to reduce the charge recombination and prolong

262 be interpreted by assuming that addition of methanol to water produces a different variation of pH o

263 e determined as temperature of 59 degrees C, methanol to water ratio of 65.2% (v/v), and extraction t

264 independent variables including temperature, methanol to water ratio percent, and sonication time wer

265 le-atom electrocatalyst with carbon monoxide/methanol tolerance for the cathodic oxygen reduction rea

266 ds ORR, besides excellent stability and good methanol tolerance in both basic and acidic electrolytes

267 fect of blue maize extracts obtained by acid-methanol treatment on the nutritional in vitro starch fr

268 external Bronsted acid proton source (water, methanol, trifluoroethanol, and phenol) that is required

269 sts for methane activation and conversion to methanol under mild conditions are methane monooxygenase

270 -1000 are active for oxidation of methane to methanol under mild reaction conditions.

271 duction of ethane (up to 94% selectivity) or methanol (up to 54% selective); the yield of MeOOH can b

272 rst time a new strategy for the detection of methanol using fluorescence spectroscopy and photoelectr

273 , then the selective oxidation of methane to methanol using molecular oxygen is possible.

274 lthough methane can be directly converted to methanol using molecular oxygen under mild conditions in

275 (3:2:1, v/v/v) and diluted with acetonitrile-methanol (v/v; 80:20) before the method was applied.

276 udy determines the antioxidant properties of methanol vegetable extracts from raw vegetables, convent

277 fectively in the production of propanal from methanol (via carbon monoxide and hydrogen) and ethylene

278 x-covered virus onto the UME while ferrocene methanol was being oxidized produced stepwise increases

279 1-Pyrene methanol was utilize to synthesize the anti-inflammatory

280 Extraction of MtbWL with chloroform-methanol-water (10:10:3) resulted in a polar lipid fract

281 An acidified methanol-water mixture was used as an effective extracti

282 Gangliosides are extracted by chloroform-methanol-water mixture, where an upper aqueous layer con

283 hod is based on extraction with an acidified methanol-water mixture.

284 pH (between 7.0 and 8.6) and composition of methanol-water mixtures (between 30 and 70% v/v of metha

285 PDMS) and low-density polyethylene (LDPE) in methanol-water solutions.

286 unit have been found to form J-aggregates in methanol-water solvent mixture and brightly emissive in

287 used for phenols, extraction with acidified methanol-water was chosen as the best to quantify the co

288 henylenediamine (DMPA), were evaluated using methanol/water and aqueous (aq) solutions.

289 ing bile salt surfactant coating with DNA in methanol/water mixed solvent and subsequent precipitatio

290 h produced the most intense ion signals from methanol/water solutions, and in ESSI MS, of dopamine (D

291 Methanol:water extracts were prepared and submitted to a

292 quenching solvent (e.g., acidic acetonitrile:methanol:water) can mitigate such problems.

293 plates, mobile phase composed of chloroform:methanol:water:25% ammonium hydroxide (70:30:4:2 v/v/v/v

294 ant compounds in the samples, extracted with methanol, were phenolic acids, syringic (2.54mg/kg) and

295 thyl salicylate undergoes hydrolysis to form methanol, which is consumed by alcohol oxidase to form f

296 e electrochemical oxidative carbonylation of methanol with CO for the synthesis of dimethyl carbonate

297 Additional minor components are methane and methanol with concentrations up to 100 ppm.

298 ted on titanium oxide, to oxidize methane to methanol with high selectivity (92%) in aqueous solution

299 s titrated into a solution of 3 in 2:1 water/methanol with NaCl, the fluorescence intensity increased

300 esence of detectable components (methane and methanol) with a concentration about 1000 times higher t