ライフサイエンスコーパス: butanol

1 under high submicellar conditions (10-25% 1-butanol).

2 hyl-2-buten-1-ol, and 300 mg/L of 3-methyl-1-butanol.

3 tion to 3-methyl-2-buten-1-ol and 3-methyl-1-butanol.

4 d the conversion of methanol to ethanol or n-butanol.

5 ctable 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol.

6 )C,(1)H] correlations in the test molecule 1-butanol.

7 ruled out by the lack of suppression by tert-butanol.

8 mulated ERK activity was also inhibited by 1-butanol.

9 However, they show increased resistance to 1-butanol.

10 an excellent pervaporation performance for n-butanol.

11 type C. thermocellum is inhibited by 5 g/L n-butanol.

12 heir capture into advanced biofuels, such as butanol.

13 cer of biofuels and bulk chemicals such as n-butanol, 1,3-propanediol, 1,3-butanediol, isopropanol, a

14 nonadienal, (E,E)-2,4-decadienal, 3-methyl-1-butanol, 1-hexanol, and 2-pentyl-furan, were employed to

15 compounds identified in this study, e.g., 1-butanol, 1-octen-3-ol, 2-and 3-methyl butanoic acid, hex

16 Hexanal, 3-methyl-1-butanol, 1-pentanol, 1-octen-3-ol, acetic acid, furfural

17 lyethylene glycol-400 (PEG-400), Transcutol, butanol-1 and butanol-2 was measured and correlated at T

18 scutol, EA, butanol-2, ethanol, EG, PG, IPA, butanol-1 and water from T=(298-318)K.

19 towards low potential (-0.12 V) detection of butanol-1 in fermentation medium (4 mM) containing multi

20 hol dehydrogenase (ADH) biocatalysis towards butanol-1 oxidation by incorporating enzymes in various

21 nol (17 vol%), i-butanol (21 vol%), and an i-butanol (12 vol%)/ethanol (7 vol%) mixture; these fuels

22 to produce four blends: ethanol (16 vol%), n-butanol (17 vol%), i-butanol (21 vol%), and an i-butanol

23 and higher alcohol esters, namely 3-methyl-1-butanol, 2,3-butanediol, ethyl lactate, 3-methyl-1-butyl

24 GC-MS identified 2-butanol, 2-butanone, 2-pentanone and 1-propanol to be po

25 duce higher alcohols including isobutanol, 1-butanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-ph

26 f yeast promoted the formation of 3-methyl-1-butanol, 2-methyl-1-propanol and 3-(methylsulfanyl)-prop

27 acetic acid, followed by hexanol, 3-methyl-1-butanol, 2-phenylethanol, 3-methylbutanal, hexanal, benz

28 ate, isoamyl acetate, isobutanol, 2-methyl-1-butanol, 2-phenylethanol, E-2-hexenol, octanal, nonanal,

29 col-400 (PEG-400), Transcutol, butanol-1 and butanol-2 was measured and correlated at T=(298-318)K.

30 10(-1) at 298 K) followed by Transcutol, EA, butanol-2, ethanol, EG, PG, IPA, butanol-1 and water fro

31 ine/1-octen-3-ol, for Venere, and 3-methyl-1-butanol/2-methyl-1-butanol, for Apollo, were also found

32 re proposed for the selective oxidation of 2-butanol: 2-butoxide and eta(2)-aldehyde.

33 s: ethanol (16 vol%), n-butanol (17 vol%), i-butanol (21 vol%), and an i-butanol (12 vol%)/ethanol (7

34 riations during smoking, of which 3-methyl-1-butanol, 3,7-dimethyl-1,3,6-octatriene, hydroxy butanone

35 including isobutanol, 1-butanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-phenylethanol from glu

36 ning emulsions had high levels of 2-methyl-1-butanol, 3-methyl-1-butanol, and 2-butanone after storag

37 : phenol +143, CaCl(2) +92.2, MgCl(2) +54.0, butanol +37.4, guanidine hydrochloride +31.9, urea +16.6

38 ation radicals were found to react with tert-butanol 4-5 times more slowly than methanol, consistent

39 ctional 2ME (4 abstraction positions) over n-butanol (5 abstraction positions).

40 The 12% i-butanol/7% ethanol blend was designed to produce no incr

41 urine 4-(methylnitrosamino)-1-(3-pyridyl)-1- butanol (a biomarker of cigarette smoke exposure) on uri

42 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol, a validated tobacco-specific marker, was measur

43 esented the highest contents of 3/2-methyl-1-butanol, acetoin and organic acids.

44 selectivity at low oxygen coverages, while 2-butanol adsorbs and desorbs molecularly on the clean Au(

45 Ethanol and propanol enhanced fusion, butanol also enhanced fusion but was less potent, and lo

46 s activation by electron transfer to yield 1-butanol and (n-Bu3Sn)2O.

47 addition to cis-2-butene-1,4-diol to form n-butanol and 1,4-butanediol, to quantify the concentratio

48 om H-bonded alkanols, the step that limits 2-butanol and 1-butanol dehydration rates; the latter two

49 l inhibition of WT-L1 adhesion was between 1-butanol and 1-pentanol.

50 hyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol and furan derivatives lik

51 hyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol was determined by means o

52 l, 1-butanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-phenylethanol from glucose, a renewable ca

53 exception of 2-methyl-1-propanol, 3-methyl-1-butanol and 2-phenylethyl alcohol, which decreased 68%,

54 prising three co-solvents (water, 2-methyl-2-butanol and acetic acid) and polyvinylalcohol 2000 (PVA2

55 d produce the characteristic solvents (i.e., butanol and acetone), but the extent of solventogenesis

56 the oxygen rebound pathway, which gives tert-butanol and acetone, or a separated radical pair.

57 talytic synthesis of butadiene from ethanol, butanol and butanediols, and (iii) the catalytic synthes

58 el to investigate the network-wide effect of butanol and butanol precursor production pathways differ

59 mes for conversion of acetyl coenzyme A into butanol and butyrate.

60 higher levels of 2-phenylethanol, 3-methyl-1-butanol and diethyl succinate, and lower concentrations

61 lventogenic Clostridium species to produce n-butanol and ethanol for use as renewable alternative tra

62 lation of the extractant phase, the acetone, butanol and ethanol mixture is upgraded to long-chain ke

63 We employ a case study of butanol and ethanol production from mixed municipal soli

64 cing in excess of 40 g of solvents (acetone, butanol and ethanol) between the completely immiscible e

65 r to a mixture of organic solvents (acetone, butanol and ethanol).

66 -propanol, 2-methyl-1-propanol, 3/2-methyl-1-butanol and ethyl octanoate were evaporated whereas the

67 These aroma compounds were 3-methyl-1-butanol and eugenol, phenethyl alcohol, 2-phenethyl acet

68 -propanol, 3-methyl-1-butanol and 2-methyl-1-butanol and furan derivatives like 5-(hydroxymethyl)-2-f

69 e synthesis is the coupling of (R)-4-nitro-2-butanol and glyoxal (trimeric form) mediated by cesium c

70 n the inhibition of the K-Shaw2 channel by 1-butanol and halothane.

71 lin and kanamycin, alcohols of ethanol and n-butanol and heavy metals of Cu(2+) and Cr(6+), were anal

72 r fermentation products include the biofuels butanol and hydrogen.

73 ptake; 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and its glucuronides (total NNAL), a biomarker o

74 ell as 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and its glucuronides (total NNAL), and cotinine

75 presence of specific radical quenchers (tert-butanol and methanol) had a similar effect on electro-ox

76 igmoidal behavior of sensitizer release in n-butanol and n-octanol occurs at an optimal temperature o

77 ons, we used a mixture of Triton X-100 and 1-butanol and observed that water-soluble natural and synt

78 56% and 44% conversions were achieved when 1-butanol and octadecanol were employed, respectively.

79 rahydrofuran, and the ring-cracking products butanol and propylene.

80 anal concentration was higher and 2-methyl-1-butanol and toluene lower for C and GSC than for GSPC.

81 alkanols (2-propanol, 1- and 2-butanol, tert-butanol) and cleavage of sec-butyl-methyl ether on POM c

82 r unburned alcohol emissions (0.17 mg/mile n-butanol, and 0.30 mg/mile i-butanol); these reductions w

83 ion of four alcohols (ethanol, 1-propanol, 1-butanol, and 1-pentanol) to the corresponding carboxylat

84 igh levels of 2-methyl-1-butanol, 3-methyl-1-butanol, and 2-butanone after storage.

85 la, Lachnospiraceae, 4-methyl-2-pentanone, 1-butanol, and 2-butanone could discriminate NAFLD patient

86 ic bacterium that produces acetate, ethanol, butanol, and butyrate.

87 al diluted solvent mixes containing acetone, butanol, and ethanol were superior or equally efficient

88 al producer of the organic solvents acetone, butanol, and ethanol.

89 urine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol, and hair and nail nicotine levels were measured

90 methyl-tert-butyl ether, acetone, pentanone, butanol, and hexanol) accumulated in the permeate collec

91 ws continuous control of n-butane, i-butane, butanol, and isobutanol diffusivities over 2-3 orders of

92 yl)-7H-pyrrolo[2,3-d]pyrimidin-4-y l]amino-1-butanol, and NBI-27914 at doses (30 mg/kg, i.p.) that di

93 at several biological processes blocked by 1-butanol are not affected by FIPI, suggesting the need fo

94 d 1,3,5-benzenetricarboxamides (BiPy-1) in n-butanol as a model system.

95 versibility of the lattice parameter using n-butanol as a retrieving agent as well as an increased la

96 Interestingly, replacing n-heptane with 1-butanol as a solvent led to a reactivity decrease of sev

97 , and the best results were found using tert-butanol as a solvent, 20 g/L of lipase B from Candida An

98 rix) are studied using water, ethanol, and n-butanol as solvents.

99 ope effect was determined to be 0.67 using 1-butanol as the substrate.

100 s-BuLi/TMEDA followed by protonation with t-butanol at -115 degrees C provided a range of new axiall

101 polyvinylpyrrolidone were dissolved in tert-butanol at different drug/polymer ratios.

102 with a magnitude that counters the effect of butanol at relevant concentrations and pressures.

103 hallenges by reporting the adaptation of the butanol biosynthetic pathway for the synthesis of odd-ch

104 de emissions showed higher emissions for the butanol blend relative to the ethanol blends at a statis

105 re the most significant carbonyls from the n-butanol blend, while formaldehyde, acetone, and 2-methyl

106 ropanal were the most significant from the i-butanol blend.

107 carbonate (DMC), diethyl adipate (DEA), and butanol (Bu)) with ultralow sulfur diesel (ULSD) at 2% a

108 oleum ether (PE)-, ethyl acetate (EA)- and n-butanol (BU)- extracts of rhubarb.

109 of chiral alcohols 1-phenylethanol (PEA), 2-butanol (BUT), and 2-pentanol (2-PEN) with the highest e

110 ted with hexane, diethyl ether, methanol, or butanol, but activity was observed with dimethyl sulfoxi

111 (2) and 5% CO(2)) in the presence of 0.05% 1-butanol, but not tertiary-butanol, stimulated PLD as evi

112 O-H bond dissociation enthalpies (BDE) in t-butanol by EPR radical equilibration technique consisten

113 Although production of 1-butanol by the fermentative coenzyme A (CoA)-dependent p

114 )H(5)C(18)OCH(3) are observed in TPD after 2-butanol (C(2)H(5)CH(16)OHCH(3)) was dosed onto Au(111) p

115 Synthesis of n-butanol can be achieved via more than one metabolic path

116 trans-2-hexenal) and alcohols (1-hexanol, 1-butanol, cis-3-hexenol) and had significant discriminati

117 0% increase in formaldehyde emissions from i-butanol, compared to certification gasoline.

118 ed models based on the structure of the LUSH-butanol complex were constructed for the wild-type and m

119 fluence of COME as a means of increasing the butanol concentration in a stable butanol-diesel blend.

120 n, Cb_3974 showed up to 2.4-fold increase in butanol concentration when compared to Cb_3904 and Cb_wi

121 kanols, the step that limits 2-butanol and 1-butanol dehydration rates; the latter two reactions show

122 /vol) O(2), CuSO(4) (0.5 microM) repressed 1-butanol-dependent induction of beta-galactosidase activi

123 e mineral salts of standard growth medium, 1-butanol-dependent induction was significantly repressed

124 ated by multi-analytical techniques prior to butanol determination in cell-free samples from an anaer

125 lete oxidation but also the water content in butanol diesel blends could cause a microexplosion mecha

126 tion for the manufacture of water-containing butanol diesel blends is reduced, and the costs are lowe

127 udy, we verified that using water-containing butanol diesel blends not only solves the tradeoff probl

128 The manufacture of water-containing butanol diesel blends requires no excess dehydration and

129 easing the butanol concentration in a stable butanol-diesel blend.

130 the properties, combustion, and emissions of butanol-diesel blends used within compression ignition e

131 example lubricity, density and viscosity) of butanol-diesel blends with respect to RME.

132 structural analog of choline, 3,3-dimethyl-1-butanol (DMB), is shown to non-lethally inhibit TMA form

133 However, 1-butanol does not always effectively reduce PA accumulati

134 ducts of these diazochlorins formed within n-butanol-doped frozen toluene matrices indicate near excl

135 solvent environment most closely resembles 1-butanol (epsilon = 17), although the energetic contribut

136 potential for butanol recovery from acetone-butanol-ethanol (ABE) fermentation broth.

137 nonical example of such processes is acetone-butanol-ethanol (ABE) fermentation by Clostridium acetob

138 Acetone, a product of acetone-n-butanol-ethanol (ABE) fermentation, harbours a nucleophi

139 an industrial organism for anaerobic acetone-butanol-ethanol (ABE) fermentation.

140 esponses of Escherichia coli (DH5alpha) to 1-butanol exposure (1.2% [vol/vol]).

141 pic responses of E. coli to 1.2% (vol/vol) 1-butanol exposure included the following: (i) decreased s

142 se optimization of compounds isolated from n-butanol extract of I. stolonifera (BE-IS).

143 -acetylcholinesterase activity was higher in butanol extract, whereas the ethyl acetate extract had t

144 antioxidant compound contained in the fruit butanol extract.

145 ACE-inhibiting effect was observed following butanol extraction due to accumulation of hydrophobic pe

146 ve acetone/hexane extractions, mild solvent (butanol) extractions, cyclodextrin extractions, and two

147 80% of the total ACE-inhibiting potential of butanol extracts from plant protein hydrolysates could b

148 nt with petroleum ether, ethyl acetate and n-butanol extracts of rhubarb in a rat model of CRF with a

149 ation in cell-free samples from an anaerobic butanol fermentation.

150 l, the CNTs/PDMS hybrid membrane with higher butanol flux and selectivity should have good potential

151 In addition, the butanol flux and separation factor increased dramaticall

152 l for the improvement of butanol recovery in butanol flux and separation factor.

153 or Venere, and 3-methyl-1-butanol/2-methyl-1-butanol, for Apollo, were also found to act as ageing in

154 as compared to the hexane, chloroform, and n-butanol fractions, as well as the crude extract.

155 high enantioselectivity for producing (S)-2-butanol from 2-butanone that was unaffected by modulator

156 od potential for pervaporation separation of butanol from ABE fermentation broth.

157 me the direct photosynthetic production of 1-butanol from cyanobacteria Synechococcus elongatus PCC 7

158 filled with 10 wt% CNTs was used to separate butanol from the butanol/water solution at 80 degrees C.

159 1-Butanol had no effect on Cch-stimulated Pyk2, Ras, and R

160 ers by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol had similar severity of lung injury as patients

161 n-Butanol has several favourable properties as an advanced

162 The results obtained with butanol/HCl and vanillin/HCl were higher than with BSA/F

163 noids (by HPLC-DAD) and proanthocyanidins (n-butanol/HCl assay), reducing capacity (ferric ion reduci

164 proanthocyanidins by depolymerisation with n-butanol/HCl, flavonols by HPLC-DAD, reducing capacity by

165 with four methods of tannin quantification: butanol/HCl, vanillin/HCl, BSA/FeCl(3) and PVPP/Folin-Ci

166 ated in PTW-cured products, such as 3-methyl-butanol, hexanal and 2,3-octanedione, while six substanc

167 e (CB-aPP) conjugate (1) from a 0.1% (w/w) n-butanol/hexane solution onto highly oriented pyrolytic g

168 urine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol identified 27 of the 28 nonsmokers by history ei

169 urine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol identified considerably more active smokers than

170 bene reaction with alcohols (ethanol or tert-butanol) identified by an absorption band at 1694 cm(-1)

171 ng 100 mM sodium dodecyl sulfate (SDS) and 1-butanol in 10 mM sodium-phosphate (pH 7.2) at a flow rat

172 ha H16, to produce isobutanol and 3-methyl-1-butanol in an electro-bioreactor using CO(2) as the sole

173 nsation of two different nitrochalcones in n-butanol in the presence of CH(3)COONH(4) at reflux follo

174 om readily available aldehydes and 4-nitro-1-butanol in three steps.

175 Since 4-nitro-1-butanol in turn is prepared in two steps via Michael add

176 1-Butanol increased Cch-stimulated protein secretion and d

177 actosidase activity, was used to show that 1-butanol induced the BMO promoter in the presence or abse

178 Moreover, S6 also reduces butanol-induced lipopolysaccharide release from the oute

179 ve the strong O-H bonds of methanol and tert-butanol instead of their weaker C-H bonds, representing

180 rface can promote the partial oxidation of 2-butanol into 2-butanone with near 100% selectivity at lo

181 The addition of water-containing butanol introduced a lower content of aromatic compounds

182 Bio-based production of n-butanol is becoming increasingly important for sustainab

183 t, the liquid-crystal phase in supercooled n-butanol is found to inhibit transformation to the crysta

184 t the putative liquid-liquid transition in n-butanol is in fact caused by geometric frustration assoc

185 ets made of cetyltrimethylammonium bromide/1-butanol/isooctane.

186 rate and ethyl 2-methylbutyrate), 3-methyl-1-butanol, isopropyl acetate, and finally the two sulfides

187 s with 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol levels consistent with active smoking and was ro

188 s with 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol levels in the active smoking range were younger

189 Urine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol levels were consistent with active smoking in 36

190 ctable 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol levels.

191 catalyst system toward chemically similar 1-butanol makes it possible to synthesize the competent Gu

192 emplified in this work for n-butane/methane, butanol/methanol, and butanol/water pair systems.

193 under micellar conditions using 1-2% (v/v) 1-butanol mobile phase to remove plasma proteins and conce

194 Sixteen model VOCs (tetrahydrofuran, butanol, n-propanol, iso-propano, acetone, methanol, eth

195 nol oligomers and promote dimeric H-bonded 2-butanol networks.

196 L) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) (0.2 ng/L) along with the reduction of NI

197 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and its glucuronides (sum of which is den

198 K) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) as the targets, we first developed a soli

199 bolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) in urine is frequently used as a biomarke

200 e, and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), a metabolite of the powerful lung carcin

201 ), and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), NNAL-N-beta-glucuronide, and NNAL-O-beta

202 rinary 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL).

203 arker [4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL)], an established biomarker (cotinine), an

204 bolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol [NNAL]) and VOCs (including metabolites of the t

205 conditions were: a ratio of crude extract/t-butanol of 0.87 (v/v), saturation in ammonium sulphate o

206 ibit the formation of extended liquid-like 2-butanol oligomers and promote dimeric H-bonded 2-butanol

207 bond cleavage in the partial oxidation of 2-butanol on oxygen precovered Au(111) is provided using t

208 orption coefficients of different isomers of butanol on poly(methyl methacrylate) sheets, zinc oxide

209 ns with or without a OH radical scavenger (2-butanol) on the SOA mass and thermal characteristics usi

210 roducts due to the strong chemisorption of 1-butanol onto the Bronsted acid sites.

211 Two solvent media containing 100% butanol or a mixture of chloroform/methanol (2:1, v/v) c

212 ) oxides for Pd-NZVI reacted with TCE in the butanol organic phase compared to Fe(II) oxides in the a

213 3e(-) per mole of Fe(0)) from Pd-NZVI in the butanol organic phase compared to the same reaction with

214 r degradation rate (kobs of 0.413 day(-1) in butanol organic phase versus 0.099 day(-1) in aqueous ph

215 VI (RL-Pd-NZVI) when reacted with TCE in a 1-butanol organic phase with limited amounts of water resu

216 calculations show that energy barriers for n-butanol oxidation increase in the order of alpha < O < Y

217 rong evidence for the C-O bond cleavage in 2-butanol partial oxidation to 2-butanone.

218 n of 1-hexanol production by extending the 1-butanol pathway provides the possibility to produce othe

219 free volumes in polymer chains to facilitate butanol permeation.

220 Facile deprotection in hot butanol permits the rapid, multicomponent construction o

221 igate the network-wide effect of butanol and butanol precursor production pathways differing in energ

222 has led to the development of an ethanol-to-butanol process operated at a lower temperature.

223 hol emissions of 1.38 mg/mile ethanol, while butanols produced much lower unburned alcohol emissions

224 w partial re-assimilation of CO2 and H2 by n-butanol-producer C. beijerinckii.

225 ent alcohol dehydrogenase (YqhD) increased 1-butanol production by 4-fold.

226 lar biologists who are enhancing ethanol and butanol production by genetic manipulation.

227 at relatively low productivity (e.g. maximum butanol production is around 20 g/L).

228 A, NFS1, ADH7 and ARO10(*), we achieved an n-butanol production of 835 mg/L in the final engineered s

229 enes identified previously; meanwhile, the n-butanol production was also improved by overexpression o

230 Correspondingly, butanol production was up to 1.2-fold greater in furfura

231 nd syringaldehyde with improved capacity for butanol production.

232 sents a promising alternative platform for n-butanol production.

233 Not only did the self-provided oxygen of butanol promote complete oxidation but also the water co

234 f practically unreactive compounds (acetone, butanol, propionic, and butyric acids).

235 yst for the Guerbet reaction of ethanol to 1-butanol, providing turnover numbers up to 725 000 Ru(-1)

236 ion of Maillard reaction products 3-methyl-1-butanol, pyrazine, 2-ethylpyrazine, 2-ethyl-3-methylpyra

237 ng iso-butyl chloroformate in an aqueous iso-butanol/pyridine environment.

238 Three reactive species (tert-butanol, quinone, and ammonium oxala) were identified in

239 was fabricated to evaluate its potential for butanol recovery from acetone-butanol-ethanol (ABE) ferm

240 brane were beneficial for the improvement of butanol recovery in butanol flux and separation factor.

241 The maximum total flux and butanol separation factor reached up to 244.3 g/m(2).h a

242 0.4M perchloric acid and purification with 1-butanol significantly shortened sample preparation (30mi

243 drogenation reaction of cyclohexanone in a 2-butanol solvent 10x faster than their hydrophilic analog

244 e to a greater extent than the liquid-like 2-butanol solvent present in hydrophilic Sn-Beta, giving r

245 These different intraporous 2-butanol solvent structures manifest as differences in th

246 conversion was achieved in acetone and tert-butanol solvent systems, respectively.

247 resence of 0.05% 1-butanol, but not tertiary-butanol, stimulated PLD as evidenced by accumulation of

248 y extending the coenzyme A (CoA)-dependent 1-butanol synthesis reaction sequence catalyzed by exogeno

249 sed to 60.74% and 65.73% in acetone and tert-butanol system, respectively.

250 ester production increased to 62.9% in tert-butanol system, unlike acetone system.

251 nts (ethanol (EtOH), isopropanol (IPA), tert-butanol (TBA) and tetrahydrofuran (THF)) and a combinati

252 solution containing H2O2 (1 mM) and tertiary butanol (tBuOH, 0.5 mM) in excess over the trace compoun

253 st time that their rapid phase transfer to a butanol/TCE organic phase can be achieved by adding NaCl

254 ehydration of alkanols (2-propanol, 1- and 2-butanol, tert-butanol) and cleavage of sec-butyl-methyl

255 ic acid, isopropanol, sodium azide, and tert-butanol) that are commonly employed to study photodegrad

256 n with 3 variables (ratio of crude extract/t-butanol, the ammonium sulphate saturation and pH) were u

257 ends of B2 with 10% and 20% water-containing butanol, the POP emission factors were decreased by amou

258 (0.17 mg/mile n-butanol, and 0.30 mg/mile i-butanol); these reductions were offset by higher emissio

259 -1-ol, 3-methyl-2-buten-1-ol, and 3-methyl-1-butanol, three C5 alcohols that serve as potential biofu

260 ing of Saccharomyces cerevisiae to produce n-butanol through a synergistic pathway: the endogenous th

261 r the conversion of ethanol (up to 37%) to n-butanol, through the Guerbet process, has been developed

262 A similar increase was also observed when butanol titer in solution increased from 10 g/L to 25 g/

263 Ala-33, increased the alcohol cutoff from 1-butanol to 1-decanol.

264 Addition of 2 equiv of tert-butanol to [Li(DME)(3)][U(CH(2)SiMe(3))(5)] generates th

265 study was conducted for the isoelectronic n-butanol to highlight the consequences of replacing the Y

266 ammonium sulphate concentration, ratio of t-butanol to slurry, solid loading and pH.

267 tection limits (3sigma) ranged from 22 ng (n-butanol) to 174 ng (2-pentanone) depending on the volati

268 ntroducing this mutation recapitulated the n-butanol tolerance phenotype.

269 th adaptation in a chemostat, we increased n-butanol tolerance to 15 g/L.

270 ed with S6 exhibits a twofold improvement in butanol tolerance, a relevant feature to achieve within

271 of the studied VOCs (2-propanol, acetone, n-butanol, toluene, 1,2,4-trimethylbenzene) at relative hu

272 s growth, a morphological stress response to butanol toxicity in E. coli, is observed in untreated ce

273 lytical methodologies were applied to both 1-butanol-treated and control cells to draw correlations w

274 y-defective constructs (PLD2-K758R) and by n-butanol treatment of cells.

275 bility and linear response (up to 14.6 mM of butanol) under very low applied potentials (from -0.02 t

276 3-butanediol, N-acetylneuraminic acid, and n-butanol using S. marcescens.

277 n untreated cells after incubation with 0.9% butanol (v/v), but is mitigated by S6 treatment.

278 -propanol, 3-methyl-1-butanol and 2-methyl-1-butanol was determined by means of head space solid phas

279 ory or 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol was not associated with acute respiratory distre

280 urine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol was significantly associated with acute respirat

281 3-Methyl-1-butanol was the major compound identified in the ferment

282 comprising of water, ammonium sulphate and t-butanol, was explored for extraction of oleoresin and gi

283 sport through the membranes was tested using butanol/water and ethanol/water mixtures due to their im

284 for n-butane/methane, butanol/methanol, and butanol/water pair systems.

285 % CNTs was used to separate butanol from the butanol/water solution at 80 degrees C.

286 The solvent system was n-butanol:water:acetic acid (84:14:7).

287 noate, whereas phenyl ethanol and 3-methyl-1-butanol were dominating alcohols.

288 e TSNA 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol were identified and quantified in authentic drin

289 one, 2-pentanone, 2-heptanone and 3-methyl-1-butanol were identified as relevant VOCs for Lactobacill

290 one, 2-pentanone, 2-heptanone and 3-methyl-1-butanol were identified as relevant VOCs for Lactobacill

291 2-Butanone and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lac

292 2-Butanone and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lac

293 Incubating embryos with 1-butanol, which diverts production of phosphatidic acid t

294 of PA is inhibited by the primary alcohol 1-butanol, which has thus been widely employed to identify

295 was a Mitsunobu reaction with perfluoro-tert-butanol, which incorporated a perfluoro-tert-butyl group

296 sistant membrane fractions is inhibited by 1-butanol, which subverts production of phosphatidic acid

297 tained from the combination of biodiesel and butanol, while there was no penalty in regulated gaseous

298 synthesize the competent Guerbet substrate 1-butanol with >99% selectivity.

299 s were observed with methanol, propanol, and butanol, with ethanol being the most potent.

300 n from flour defatted with water-saturated 1-butanol (WSB; extracted at 20 degrees C) and 2-propanol

301 h adenoviruses overnight or the inhibitors 1-butanol, Y-27632, or C3 exotoxin before stimulation with