ライフサイエンスコーパス: organic solvent

1 are soluble solely in mixtures of water and organic solvent.

2 ed throughout the solution in the absence of organic solvent.

3 oiety with an amine-containing surfactant in organic solvent.

4 cetyltrimethylammonium chloride (CTMA) in an organic solvent.

5 c drug Phenytoin, with no use of any harmful organic solvent.

6 anol mixtures with the high (90%) content of organic solvent.

7 in water and UV-initiated polymerisation in organic solvent.

8 lly perform label-free monitoring of various organic solvents.

9 ical and thermal stability and solubility in organic solvents.

10 ic nanostructures that are highly dynamic in organic solvents.

11 nm, while retaining their high permeances to organic solvents.

12 fluence the response of soil microbes to the organic solvents.

13 cal manipulations employing large volumes of organic solvents.

14 side of the molecules, even in highly polar organic solvents.

15 at promise as enzyme mimics that function in organic solvents.

16 her yields than in pure water or many common organic solvents.

17 borate syntheses, tedious purifications, and organic solvents.

18 dienophiles requiring mixtures of water and organic solvents.

19 phobic species from water without the use of organic solvents.

20 mising for discrimination of closely related organic solvents.

21 ry is usually carried out in either water or organic solvents.

22 fficiency have typically been synthesized in organic solvents.

23 but still play a major role in fluorous and organic solvents.

24 lubility of the 25 260 Da compound in common organic solvents.

25 ed phenols towards the chemical treatment by organic solvents.

26 e nanoparticles dispersed in a wide range of organic solvents.

27 bicity increases with decreasing polarity of organic solvents.

28 t fractionation processes, which make use of organic solvents.

29 furon was carried out in 16min without using organic solvents.

30 psules, which in contrast can be employed in organic solvents.

31 with other polymers, able to withstand most organic solvents.

32 of functionalized SWNTs that are soluble in organic solvents.

33 own, and is compatible with both aqueous and organic solvents.

34 een used to detect trace amounts of water in organic solvents.

35 s (HBAs) and neutral H-bond donors (HBDs) in organic solvents.

36 onic hydrogel insoluble in either aqueous or organic solvents.

37 nation polymer nanotubes upon treatment with organic solvents.

38 eaction catalysis in the presence of various organic solvents.

39 h volatility and low surface tension of most organic solvents.

40 es are comparable to those observed in polar organic solvents.

41 .5Te3 or n-type Bi2Te2.7Se0.3), binders, and organic solvents.

42 omplex in high yield in several common polar organic solvents.

43 formational differences of MK-2 in different organic solvents.

44 talyst reusability, and precludes the use of organic solvents.

45 non-chlorinated solvent and small amounts of organic solvents.

46 e are the high efficiency and the absence of organic solvents.

47 conditions, without the need for voltage or organic solvents.

48 nown about their supramolecular chemistry in organic solvents.

49 poly(N-isopropylacrylamide) (poly(NIPAM)) in organic solvents.

50 or high reactivity while limiting the use of organic solvents.

51 of ferromagnetic nanoparticles in aqueous or organic solvents.

52 e is generally carried out using chlorinated organic solvents.

53 is similar to that of analogous compounds in organic solvents.

54 le to corrosive aqueous solutions and common organic solvents.

55 e-variable-at-a-time methodology as follows: organic solvent: 1-octanol+2.5% (V/V) di-(2-ethylhexyl)

56 The organic solvent (50% (v/v) ACN) assisted the immobilized

57 itectures was achieved without the use of an organic solvent, a secondary emulsifier, or high-energy

58 s because GO membranes appear impermeable to organic solvents, a phenomenon not yet fully understood.

59 torical use as an industrial producer of the organic solvents acetone, butanol, and ethanol.

60 species that ferments sugar to a mixture of organic solvents (acetone, butanol and ethanol).

61 methods consisting of three extractions with organic solvents (acetonitrile, methanol, and methanol/e

62 from a single biological extract, using 80% organic solvent (ACN:MeOH:H2O 2:2:1).

63 ge of pKa values, we suggest that an aprotic organic solvent affects the reaction kinetics by changin

64 Nanoharvesting eliminates the use of organic solvents, allows spectral identification of the

65 NaCl solution of large volume to extract the organic solvent and harden the embryonic microspheres.

66 igher-order structures were obtained in both organic solvent and in water.

67 s efficiently under mild basic conditions in organic solvent and may therefore also enjoy synthetic u

68 Samples are extracted with a small amount of organic solvent and most of lipids in the extract were r

69 t distribution was different from that in an organic solvent and was also dependent on the length of

70 Different combinations of organic solvents and acids were screened for their abili

71 ines at elevated temperature in a mixture of organic solvents and aqueous CH3CO2H, which catalyzes im

72 compounds are effective gelators for several organic solvents and aqueous solutions.

73 d fluorescence properties were determined in organic solvents and aqueous surfactants.

74 It is soluble in common organic solvents and can be easily sublimed as a crystal

75 itions were optimized by comparing different organic solvents and enzymes.

76 Effect of water, organic solvents and five different aqueous surfactant f

77 the pigments are rendered highly soluble in organic solvents and in polymers and show pH-dependent a

78 ] (1) in the presence of water in a range of organic solvents and is also slowly converted in the sol

79 Gamma-oryzanol was extracted with organic solvents and its extracts were characterized by

80 evated temperature, ion strength, buffer pH, organic solvents and keeping time.

81 rate detection and identification of similar organic solvents and mixtures of such solvents.

82 d phase separation in mixtures of water with organic solvents and potentially water purification.

83 dified proteins that can be transferred into organic solvents and represent the structural material o

84 rsion reaction has been performed in several organic solvents and room-temperature ionic liquids (RTI

85 P is tested to be soluble in a wide range of organic solvents and shown to possess reactive Fp end gr

86 pproximately 1000 times higher than those in organic solvents and strongly enthalpically favored at 2

87 (-1) in aqueous solutions without the use of organic solvents and time-consuming multiple centrifugat

88 tion included the addition of trace water to organic solvents and trace organic liquids to water.

89 The formulation protocol did not involve organic solvents and was rapid and efficient as confirme

90 As anticipated, this peptide forms gels in organic solvents and water via hydrogen-bonded beta-shee

91 ed" clays, in as-received and "contaminated" organic solvents and water, at 60 degrees C and atmosphe

92 This compound is chemically stable in organic solvents and water.

93 e the reactions in brine, without the use of organic solvent, and by employing an almost stoichiometr

94 tionary phase, mobile phase pH, temperature, organic solvent, and gradient slope) and different isoto

95 device reproducibility, toxic and hazardous organic solvent, and incompatibility with scalable fabri

96 Experiments were carried out in dry organic solvent, and the results showed that, although a

97 uding coating with photoresist, washing with organic solvent, and thermal annealing.

98 lize Pickering emulsions formed by water and organic solvents, and also, gas-filled g-C3N4 frameworks

99 fects of the use of surfactants and volatile organic solvents, and deepens our understanding of inter

100 ar (methanol) and nonpolar (dichloromethane) organic solvents, and is hypothesized to arise from redo

101 tization is a one-step reaction, requires no organic solvents, and is safe, as the derivatizing agent

102 olvatochromism of each dye was studied in 28 organic solvents, and it was found that all compounds ex

103 mpatibility, excellent resistance to various organic solvents, and its ability to withstand relativel

104 CdS nanocrystals requires Cu(I) precursors, organic solvents, and neutral atmosphere, but these cond

105 elevated temperature and in the presence of organic solvents, and provides a simple platform for int

106 aphene oxide (S-rGO) membranes are stable in organic solvents, and strong acidic, alkaline, or oxidat

107 drogen-containing molecules persist in polar organic solvents, and the spectral evolution of the DF p

108 The macrocycles are freely soluble in common organic solvents, and their identities were confirmed by

109 skite films are soluble in most of the polar organic solvents, and thus until now, they were not cons

110 lly available MS-compatible surfactants, two organic solvents, and two chaotropes on the enzymatic di

111 Our approach enables the facile synthesis of organic solvent- and water-soluble nearly monodisperse n

112 LTCC technology, such as high-temperature or organic solvents applications, while using a simple fabr

113 Instead, we find that molecules soluble in organic solvents are dependent upon MHC class II and rec

114 t for Fischer glycosidations in low-polarity organic solvents are described.

115 ult indicates that halide-pi interactions in organic solvents are mainly driven by enthalpy.

116 arge carrier mobility and high solubility in organic solvents are overviewed.

117 Organic solvents are ubiquitous in occupational settings

118 -), Br(-), I(-), NO3(-) and quinuclidine, in organic solvent) are described.

119 ly, a rearrangement product not formed in an organic solvent arising from the triplet radical pair ge

120 In the absence of an organic solvent as the reaction medium, organic waste an

121 ns of CDs was similar to that obtained using organic solvents as ethanol.

122 However, there is limited information on organic solvents as human breast carcinogens.

123 ased cycloaddition endo-effects (relative to organic solvents) as do in-water reactions.

124 hemical oxidation of the Ir(IV,V) complex in organic solvents at 1.9 V vs NHE.

125 -H6](2-) (1), reacts with carbon monoxide in organic solvents at 40 degrees C to cleanly form an enca

126 Effects of various binary organic solvents at different temperatures on the remova

127 The progressive replacement of organic solvent-based coatings by waterborne latex polym

128 n the POT film was in direct contact with an organic solvent-based electrolyte.

129 ow for great printability of both water- and organic solvent-based inks thus facilitating the full-in

130 emonstrate high efficiencies in deoxygenated organic solvents but do not function in air-saturated aq

131 ions that are difficult to be carried out in organic solvents but have shown a beneficial effect when

132 gments to be strong enough for folding in an organic solvent, but weak enough to prevent aggregation

133 s were first stabilized for dispersion in an organic solvent by coating with 1, 2-dioleoyl-sn-glycero

134 s were successfully generated in a number of organic solvents by the reaction between shelf-stable re

135 man, tabun, VX and their mimics, in water or organic solvent, by qualitative fluorescence patterns an

136 actors are one measure of waste created, and organic solvents, by far, are the main contributors to t

137 t endo:exo ratios, when compared to those in organic solvents, can be used to distinguish between the

138 lyst system, previously described for use in organic solvents, can hydrogenate CO2 to formate in wate

139 (i.e., in the absence of structure-inducing organic solvents) CGRP preferentially populates conforma

140 ies, a dramatic enhancement of solubility in organic solvents (CH2Cl2, CHCl3) is observed for n >/= 8

141 nd switching properties of the polymer in an organic solvent (CHCl(3)).

142 e performed under inert atmospheres in toxic organic solvents, chemoselective addition of organolithi

143 The alkoxy-terminated SiQDs are soluble in organic solvents, colloidally stable, and show bright an

144 ormed in the chemical industry take place in organic solvents, compounds that are generally derived f

145 nsitivity decreased by a factor of 2 at high organic solvent concentrations.

146 t phenolics are usually associated with high organic solvent consumption and long extraction times.

147 ification, our method reduced the per sample organic solvent consumption from 450 to 30mL per sample

148 h a reduced chromatographic run (<7 min) and organic solvent consumption, and requires only standard

149 Due to the low organic solvent consumption, FPSE meets all green analyt

150 UHPLC method allowed reduction of the organic solvents consumption (8 times lower) and decreas

151 nge of 2-13, ionic strength of 10-100 mM and organic solvent content from 0% to 40%.

152 e in ionic liquids (ILs), three conventional organic solvents (COS), and water is studied by (31)P NM

153 Preserving DNA hybridization in organic solvents could someday serve to significantly ex

154 Fullerene C60, co-introduced via an organic solvent, did not influence the response of soil

155 corporation of a chelating agent in a common organic solvent, dimethyl sulfoxide (DMSO).

156 hosphorene flakes are thinner than anhydrous organic solvent dispersions, thus allowing the observati

157 or the model compound fluorescein, where the organic solvent DMSO is exchanged against an aqueous buf

158 ipid bicontinuous cubic single crystals: (i) organic solvent drying speed, (ii) membrane charge densi

159 d by mixing lipids and lipidated peptides in organic solvent (e.g., chloroform).

160 ldosterone from the cell culture medium into organic solvent enabled the development of 96- and 384-w

161 exfoliated MoS2 sheets in high boiling point organic solvents enabled by surface functionalization an

162 process, such as the influence and amount of organic solvent, enzyme amount, pH and extraction temper

163 ovalbumin >90% reduction of OVA present) and organic solvent (ethanol >95% reduction) in less than 4

164 ration) and consuming only 0.85mL of a green organic solvent (ethanol).

165 s of ripe pistachios were extracted with two organic solvents (ethanol and methanol) and characterize

166 e and active in both water and the renewable organic solvent ethyl lactate.

167 ing devices as a mediator, e.g. fullerene in organic solvents exhibits five stages of reversible oxid

168 ive couplings-processes that usually require organic solvents, expensive and often dangerous coupling

169 phosphonoglycans were purified by sequential organic solvent extractions, methanol precipitation, and

170 Antioxidant behaviour of aqueous/organic solvent extracts and essential oil as well as th

171 se exhibited by the dilute RuPZn cofactor in organic solvent: femtosecond, nanosecond, and microsecon

172 ated to dryness under nitrogen, dissolved in organic solvent followed by reaction with TFAI.

173 OHE) system that uses draw solutions with an organic solvent for enhanced thermal separation efficien

174 Cells were rapidly transferred into ice-cold organic solvent for instantaneous extraction of the cell

175 se of dimethyl sulfoxide (DMSO) acting as an organic solvent for simultaneous sample analyte solubili

176 stable in a nitrogen atmosphere or in select organic solvents for at least one month.

177 rformed under solvent-free conditions and in organic solvents for comparison.

178 ls, such as rapeseed oil, as alternatives to organic solvents for dispersion of CNTs.

179 such as time of saponification, the type of organic solvents for fat extraction, the stationary phas

180 cessible using established methods), unusual organic solvents for metabolite isolation and microbial

181 -IL-DLLME using low-density ionic liquid and organic solvents for preconcentration of Sb and Sn.

182 ne), PDMS) against the 36 most commonly used organic solvents for small-molecule crystallization stud

183 new procedure is simple, convenient, almost organic solvent free, and causes far less damage to the

184 A biomimetic approach to organic solvent-free microencapsulation of proteins base

185 An organic solvent-free microextraction was proposed as a s

186 SOM compounds by a combination of different organic solvents from soils with a wide range of C conte

187 set comprised retention data of combined pH/organic solvent-gradients, where the organic content was

188 rs intrinsic to the cell wall partition into organic solvents; however, these responses are not expla

189 ging with dosing restrictions and the use of organic solvents impacting on both the bioactivity and t

190 sequences of tube radial distribution of the organic solvent in an aqueous-organic system within the

191 hese techniques have thus far used anhydrous organic solvents in an effort to minimize exposure to kn

192 Emerging evidence has also implicated organic solvents in the development of this difficult-to

193 e dispersed and exfoliated both in water and organic solvents in the presence of two different PDI de

194 An alternative to organic solvents in which cross-couplings are run can be

195 l order in >/=90% (vol/vol) of several polar organic solvents including tetrahydrofuran (THF) and iso

196 was found to: a) obviate micronization- and organic solvent-induced TT degradation, b) improve antig

197 th nanoparticles prior to ultrafiltration or organic-solvent-induced protein precipitation for optima

198 been proposed, including ultrafiltration and organic-solvent-induced protein precipitation, there is

199 more susceptible to denaturation by a water-organic solvent interface than its glycoconjugates, impo

200 pull out the upconversion nanoparticles from organic solvent into an aqueous phase.

201 processing industry involves large losses of organic solvent into the atmosphere and long extraction

202 The protocol is such that no organic solvent is involved at any stage; from the react

203 reservation without the need for any (toxic) organic solvents is reported.

204 with beta-cyclodextrins, without the use of organic solvents, is described.

205 more, water, rather than traditional aprotic organic solvents, is used to dissolve the precursors.

206 crobial activity of WGO and PGO delivered in organic solvent (isopropanol) showed dose-dependent anti

207 nd their photophysical properties in various organic solvents, laser performances, and photostabiliti

208 ous sample donor phase through an immiscible organic solvent layer acting as a filter phase into a li

209 r and prevent DNIC 1 from dimerization in an organic solvent (MeCN).

210 tive compounds and the effectiveness of four organic solvents (methanol, ethanol, acetone and diethyl

211 ectively in PCR screening as DNA purified by organic solvent methods, are stable for up to 1 year at

212 y of synthesis procedure, low consumption of organic solvent, mild working temperature during the syn

213 New immunosensors working in organic solvent mixtures (OPIEs) for the analysis of tra

214 ry out in the presence of solids or volatile organic solvents, most of the synthetic "toolkit" cannot

215 mer conjugates in good yields (up to 40%) in organic solvents (N,N-dimethylformamide, N,N-dimethylace

216 We found that the common organic solvent, N,N-dimethylacetamide (DMA), prevents e

217 The potential of ultrathin GO laminates for organic solvent nanofiltration is demonstrated by showin

218 Membrane performance in organic solvent nanofiltration was evaluated on the basi

219 lene glycol (PEG) continuous phase (using an organic solvent not penetrating into dextran matrix).

220 e of NaClO2/TEMPO/NaClO in either aqueous or organic solvent, not only allows the Calpha-H oxidation

221 Rate accelerations (k(rel)) in organic solvents of up to 2.4 x 10(8) are observed.

222 between the surface energies of aqueous and organic solvents on a Teflon substrate, a fully automate

223 aggregates of different particle size or via organic solvents on soils with different organic matter

224 ied to quantify the effects of polar aprotic organic solvents on the acid-catalyzed conversion of xyl

225 The effect of pH and organic solvents on the extraction efficiency was invest

226 of surfactant type, concentration and common organic solvents on the extraction of TPC and AA (%) was

227 be amorphous or crystalline, and soluble in organic solvents or aqueous media.

228 pure water as a spray solvent instead of the organic solvents or aqueous mixtures normally used.

229 nd produce quantitative yield of ligation in organic solvents or aqueous solutions.

230 1) template DNA without requiring the use of organic solvents or centrifugation steps.

231 Addition of polar organic solvents or common anions to the ensembles leads

232 required final purification step, the use of organic solvents or concentrated hydrochloric acid (HCl)

233 nic surfactants, thereby avoiding the use of organic solvents or harsh chemical procedures.

234 th no need for centrifugation or filtration, organic solvents or high temperature enables its full im

235 No cyanine aggregation was observed in organic solvents or in phosphate buffer solution.

236 is issue since they rely on extractions with organic solvents or on in vitro digestion without a subs

237 e background electrolyte, in the presence of organic solvents or surfactants.

238 We attribute organic solvent permeation and sieving properties to ran

239 With increasing membrane thickness, organic solvent permeation rates decay exponentially but

240 10 nm, which translates into fast water and organic solvent permeation.

241 elop high-performance sensors for monitoring organic solvents, primarily due to the environmental imp

242 gainst extreme external stressors, including organic solvents, proteases, and ethylene oxide gas ster

243 city of C-Cl bond cleavage was reduced in an organic solvent (reaction with arene radical anions in g

244 This simple, economical, fast, and green (no organic solvent required) sample preparation scheme was

245 Omitting the extraction of oil with organic solvents resulted in a protein isolate that cont

246 used on the evaluation of quantitation using organic solvents revealed a surprisingly poor performanc

247 action, in terms of simplicity, reduction of organic solvents, sample throughput and effectiveness fo

248 pin peptides by a reactive tagging scheme in organic solvents selects for catalysts that reproduce th

249 In an organic solvent, since the cage lifetime is shorter than

250 e quantum dots were prepared in a variety of organic solvents stabilized with a quaternary ammonium h

251 itions such as heat resistance, contact with organic solvents, sterilization, storage and immobilizat

252 tection of trace amounts of water in various organic solvents such as CH3OH, THF, CH3CN, and acetone

253 ervation is the addition of large amounts of organic solvents such as glycerol or dimethyl sulfoxide,

254 emonstrated that by tuning the ratio between organic solvents such as N-methyl-2-pyrrolidinone or ort

255 Exfoliation of the hybrid material in organic solvents such as THF and chloroform yields sheet

256 At high concentrations, the presence of organic solvents, such as those present in AFFF formulat

257 Unlike organic solvent swelling effects, this chemical process

258 eveloped in our group, where a mixed aqueous-organic solvent system containing N,N-dimethylacetamide

259 a selectively insulated gold electrode in an organic solvent system showcased the response of Hg/Pt U

260 reported thus far are largely restricted to organic solvent systems, and it is likely that the move

261 standard potential of O2 reduction to H2O in organic solvents, taking into account the presence of an

262 f these cellular bodies behaves more like an organic solvent than like water.

263 l friendly because it eliminates the need of organic solvents that are typically used in separation t

264 e tether, exhibits an affinity toward C60 in organic solvents that is dramatically higher than the or

265 technique, in which the bilayers contain an organic solvent, the Montal-Mueller or solvent-free tech

266 ion of 5,6-dihydropyrimidin-5-yl radicals in organic solvent through the synthesis of new lipophilic

267 icles by weight) in aqueous solution without organic solvents through electrostatic interactions by s

268 er, adhesive droplets are prepared by adding organic solvent to an aqueous polymer solution at elevat

269 trogenase cofactors can be extracted into an organic solvent to catalyze the reduction of cyanide (CN

270 f extracted compounds via the use of limited organic solvent to desorb analytes and perform electrosp

271 11 s, and it reduces the required amount of organic solvent to do the sample preparation.

272 weight fractions of </=0.25; and varying the organic solvent to water ratio used in their preparation

273 iscipline that remains highly dependent upon organic solvents to one that will be sustainable, based

274 trasonicated in a micellar solution, free of organic solvent, to extract the analytes, and the supern

275 such as differing antibiotic resistances or organic solvent tolerances, are of keen interest both fr

276 be used to clean up different types of oil, organic solvents, toxic and corrosive contaminants.

277 n the COF membranes is incompatible with the organic solvents used for the COF IP process.

278 The amount of organic solvents used, molar efficiency, and duration of

279 60 degrees C (P<0.05), regardless of binary organic solvents used.

280 Imprinted polymers produced in organic solvent using acrylamide as a functional monomer

281 quantum dots (GOQDs) by simply changing the organic solvents utilized in the PLE processing.

282 Briefly, BAs are extracted into an organic solvent via the use of an ion pairing agent, fol

283 e size-dependence of aromatic stacking in an organic solvent was examined.

284 a triazabutadiene that is soluble in aprotic organic solvents, we noted a similar light-induced chang

285 tions of the constituents in the BGE and the organic solvent were simplified to a 1-dimensional probl

286 ly from Bene hull by a number of aqueous and organic solvents were investigated.

287 rsors) partially soluble in both aqueous and organic solvents were produced employing a relatively fa

288 Different aqueous/organic solvents were tested to isolate proteins, an ace

289 d redox potentials of MK-2 differed in three organic solvents, where MK-2 was most easily reduced in

290 -temperature reaction in aqueous mixtures of organic solvents, where the only inputs are dihydroartem

291 i(hydroperoxy)propane adducts are soluble in organic solvents which enables oxidation reactions in on

292 stered to patients, without determination of organic solvents, which reduces the overall synthesis-to

293 , hydrophilic molecules to solubilize DNA in organic solvents, which reduces the shielding around the

294 these porphyrins well-soluble in a range of organic solvents, while 5,15-meso-aryl substitution caus

295 also be carried out at high temperatures in organic solvent with high selectivity using stoichiometr

296 ursor of mixed metal-oleate complexes in hot organic solvents with dissolved sulfur sources.

297 When host 1 is dissolved in organic solvents with large solvent internal pressures (

298 ed under biphasic conditions using different organic solvents with phosphate buffer.

299 uctor nanocrystals/colloidal quantum dots in organic solvents with special emphasis on earth-abundant

300 s show outstanding separation performance in organic solvents, with up to two orders of magnitude hig