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1 s (methanol, acetone, dimethylformamide, and n-hexane).
2  also higher than in the oils extracted with n-hexane.
3 her than in their counterparts prepared with n-hexane.
4  Acetone may potentiate the neurotoxicity of n-hexane.
5 he target analytes were eluted with 20 mL of n-hexane.
6  the monobranched isomers and finally linear n-hexane.
7 n the solvents tetrahydrofuran, methanol, or n-hexane.
8  is found to be 22 times larger than in sole n-hexane.
9 lar organic liquids, such as cyclohexane and n-hexane.
10  using acetone as a modifier in CH2Cl2 or in n-hexane.
11 ht product of the metathesis of two moles of n-hexane.
12 ensemble of 1-hexanol aggregates solvated in n-hexane.
13 ion of a prototypical atmospheric pollutant, n-hexane.
14 ter, A(S) = 19 ps(-1), E(b) = 1520 cm(-1) in n-hexane.
15 m temperature range from n-heptane (0.55 M), n-hexane (0.60 M), toluene (0.65 M), MTBE (1.7 M), Et(3)
16  30 degrees C and solvent mixture of acetone/n-hexane 1:3 (v/v) provided optimal conditions for extra
17  prior to UAE using a mixture of isopropanol/n-hexane (1:1) as solvent.
18                         A mixture of acetone/n-hexane (1:1, v/v) was selected for accelerated solvent
19 od was based on sample dilution with ethanol:n-hexane (1:3, v/v), homogenization, vacuum filtration o
20 PA in the gas phase and in various solvents (n-hexane, 1-chlorohexane, acetone, and water) were estab
21 face reactions of various C(6) hydrocarbons (n-hexane, 2-methylpentane, 3-methylpentane, and 1-hexene
22                                     A single n-hexane/2-propanol extract containing both types of com
23 ), time (1-60 min), percentage of acetone in n-hexane (25-75%, v/v) and solvent volume (10-30 ml) was
24 catalytic activity for hydroisomerization of n-hexane, a reaction requiring hydrogenation/dehydrogena
25 compounds were extracted simultaneously with n-hexane/acetone/ethanol (50/25/25, v/v/v).
26 AHs in the processed meats were extracted in n-hexane after hydrolysis with methanolic KOH.
27 nto the stationary phase is very small, both n-hexane and 1-pentanol partition strongly into and ther
28 ures, we studied the adsorption behaviors of n-hexane and 2-chloroethyl ethyl sulfide to explore the
29 96 K and in the presence of excess hydrogen, n-hexane and 3-methylpentane adsorbed molecularly on Pt(
30  excess hydrogen enhanced dehydrogenation of n-hexane and 3-methylpentane to form pi-allyl c-C(6)H(9)
31 ial nonpolar S3(FC) to long-lived (1.3 ns in n-hexane and 3.4 ns in acetonitrile) polar S1.
32 products of n-hexane isomerization (140 Torr n-hexane and 620 Torr H2 at 360 degrees C).
33  (Malvaceae) was extracted successively with n-hexane and chloroform.
34                       The dehydrogenation of n-hexane and cycloalkanes giving n-hexene and cycloalken
35 ty in the wild type and Mar mutants (to both n-hexane and cyclohexane).
36 mutant resulted in loss of tolerance to both n-hexane and cyclohexane.
37 reparation involves dissolving the sample in n-hexane and extracting it with ACN.
38 f cow's milk was achieved using ethyl ether, n-hexane and isopropyl alcohol (3:3:4) mixture via solub
39                                 The solvents n-hexane and methyl n-butyl ketone are metabolized to th
40 that lower surface tension solvents, such as n-hexane and perfluoropentane, are applied.
41 s of two extraction techniques (conventional n-hexane and supercritical CO(2)) on the oil extraction
42 a coli K-12 strains are normally tolerant to n-hexane and susceptible to cyclohexane.
43 butter sample was diluted and homogenised by n-hexane and Triton X-100, respectively.
44 st step, msLLE was conducted with 1.75 mL of n-hexane, and all of the extract was vaporized through a
45 t cavities in computer simulations of water, n-hexane, and n-dodecane under benchtop conditions shows
46 ficients for the alkane solutes for both the n-hexane- and 1-pentanol-swollen stationary phases, the
47 ydrocyclization and further aromatization of n-hexane are attributed to the prominent adsorption of r
48 opane (869 cm(-1)), ethane (993 cm(-1)), and n-hexane) are well resolved in the broadband spectra acq
49 anol and trifluoroacetic acid (TFA)-modified n-hexane as the mobile phase.
50  for CH(4) over heavier hydrocarbons such as n-hexane, benzene, toluene, and o-xylene, as well as gas
51 F exhibits chromatographic separation of the n-hexane/benzene/cyclohexane mixture and demonstrates re
52 rent chromatography using the solvent system n-hexane/benzotrifluoride/acetonitrile (20:7:13, v/v/v).
53 tive concentration of PAHs while eliminating n-hexane by the FEDHS process.
54                        Whereas saturation by n-hexane causes a decrease of the alcohol partition cont
55                                     Isolated n-hexane, chloroform and ethyl acetate fractions suppres
56 owed the best performance using a mixture of n-hexane, chloroform, and dichloromethane (70 mL) for ex
57  were tested to isolate proteins, an acetone:n-hexane combination being the best protein precipitant.
58  and 30 bar in hybrid sorbents consisting of n-hexane confined in MIL-101 is found to be 22 times lar
59 D frequency shifts of solubilized deuterated n-hexane confirm that it resides in a dry, oil-like envi
60                   In particular, significant n-hexane contamination ( approximately 0.4 ng/mL) occurr
61 t reactivity in benzene hydride-transfer and n-hexane cracking reactions.
62 .8 - 7.4 nm diameter) and solvents (toluene, n-hexane, cyclohexane).
63 lity (28.5% overall), the stretched state of n-hexane does exist in the bulk solution, allowing the m
64 rections for tunneling in both gas-phase and n-hexane environments.
65  Herein, the type of organic solvents (i.e., n-hexane, ethanol, and isopropanol) and their binary mix
66 as performed on silica gel with a mixture of n-hexane, ethyl acetate and ammonia.
67 d different solvents (CS2, toluene, acetone, n-hexane, ethyl acetate) are extensively studied as well
68                              Analysis of the n-hexane extract by GC-MS led to the identification of t
69 ctane diterpenes 6-8, were isolated from the n-hexane extract of the marine sponge Svenzea flava coll
70                                  The soxhlet n-hexane extraction of these achenes produced a total oi
71                                However, with n-hexane extracts with higher purity (mg ergosterol/g ex
72 amples and an additional defatting step with n-hexane for cheese, the matrix with the highest fat con
73 een solvents offer promising alternatives to n-hexane for sustainable vegetable oil extraction.
74 n der Waals pore size of 0.42 nm to separate n-hexane from cyclohexane-despite the fact that both mol
75  indicate an adsorption selectivity order of n-hexane > 2-methylpentane > 3-methylpentane > 2,3-dimet
76 Occupational exposure to solvents, including n-hexane, has been associated with acquired color vision
77 rmined the valence-bond shift equilibrium in n-hexane (hex), n-octane (oct), and n-dodecane (dod).
78 PH3)2L (W'-L, where L = H2, N2, C2H4, CO, or n-hexane) in an effort to confirm the infrared spectrosc
79 - or 3-methylpentane, as desired products of n-hexane isomerization (140 Torr n-hexane and 620 Torr H
80                                              n-Hexane isomerization rates were limited by isomerizati
81 d support-dependent catalytic selectivity in n-hexane isomerization.
82         The array of alkanes from propane to n-hexane led to the preferential functionalization of th
83                                              n-Hexane levels above the method detection limit were, h
84 lvents, including chloroform, ethyl acetate, n-hexane, methanol, and water.
85         Samples were extracted using acetone/n-hexane mixtures at different ratios (1:3, 2:2 and 3:1,
86 o molecular dynamics simulations reveal that n-hexane molecules stretch by nearly 11.2% inside the na
87 es of atomic size in six molecular solvents: n-hexane, n-dodecane, n-undecyl alcohol, chloroform, car
88 terial, and the analytes included n-pentane, n-hexane, n-heptane, 1 -butanol, and 1-pentanol.
89 nterfacial adsorption effects for n-pentane, n-hexane, n-heptane, 1-butanol, and benzene solutes at i
90 e a new method for the analysis of alkanes ( n-hexane, n-heptane, n-octane, n-nonane, n-decane, n-und
91 e dissolution solvents used (tetrahydrofuran/n-hexane, n-hexane, or methanol) during photolysis.
92 ate that these voids preferentially allocate n-hexane, opening the way to explore further application
93 ion solvents used (tetrahydrofuran/n-hexane, n-hexane, or methanol) during photolysis.
94 m were investigated considering cyclohexane, n-hexane, or n-octane as nonclustering modifiers and iso
95                   Treating 1 with n-pentane, n-hexane, or tetramethylsilane (TMS) gave the first exam
96 thylpentane, 3-methylpentane, n-pentane, and n-hexane produce methane in situ.
97  extraction efficiency of only 28% for BA in n-hexane, recirculative TSLLE resulted in a BA recovery
98 vity of cyclization and aromatization in the n-hexane reforming reaction.
99 pite similar 1D-gel profiles, defatting with n-hexane resulted in significantly higher yields of crud
100 amework with the commensurate adsorption for n-hexane results in exceptional performance in separatin
101 extracted by ethanol/isopropanol and ethanol/n-hexane significantly showed the highest extraction yie
102                 In contrast, in an isotropic n-hexane solution, there was little difference among the
103 components in plant seed oils extracted with n-hexane (Soxhlet method) and chloroform/methanol (Folch
104 actions from ABE and ABEa, ABEa-Ea-B (80% Ea/n-hexane sub-fraction from ABE-Ea) had the most potent i
105 nol mixture would be a promising solvent for n-hexane substitution to extract this oil on an industri
106      The resulting quantification limits for n-hexane through n-decane ranged from 0.069 to 0.132 ng/
107 apacities of 2.2 mmol g(-1) in 1 min with an n-hexane to 2,2-dimethylbutane selectivity over 200 in a
108 e to form a crystalline tBu(+) salt and with n-hexane to form an isolable hexyl carbocation salt.
109  for the catalytic conversion (reforming) of n-hexane to isomers.
110  For small hydrocarbons such as n-pentane or n-hexane, two guests enter the host, and they move freel
111 heir mixed phases for the capture of gaseous n-hexane, used as a structural mimic for the chemical wa
112 min, a solvent composition of 25% acetone in n-hexane (v/v) and solvent volume 40 ml.
113 hase composition: (i) a helium vapor, (ii) a n-hexane vapor, and (iii) a 1-pentanol-saturated helium
114 d as sorbent and an extra cleaning step with n-hexane was added.
115 A polymer and PAHs, only the latter, and not n-hexane, was adsorbed by the sorbent.
116 action steps; 1-5) and two clean-up methods (n-hexane washing vs. low temperature fat precipitation)
117 on-sonicated counterpart (LLE-agitation) and n-hexane washing.
118 was used for rinsing, while acetonitrile and n-hexane were used as elution solvents.
119 lar (methanol, acetone, dichloromethane, and n-hexane) were selected to maximize the number of compou
120 ytic isomerization and dehydrocyclization of n-hexane, which are the important "reforming" reactions
121 and lupeol acetate (1, 2) were isolated from n-hexane while betulin, B-sitosterol, B-amyrin, oleanoli
122 deal temperature (70 degrees C) and solvent (n-hexane) with extraction yield of 97.30% +/- 3.98 was o
123        PCA grouped the green solvents, while n-hexane yielded a distinct profile.

 
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