ライフサイエンスコーパス: n-hexane

1 her than in their counterparts prepared with n-hexane.

2 Acetone may potentiate the neurotoxicity of n-hexane.

3 ion of a prototypical atmospheric pollutant, n-hexane.

4 he target analytes were eluted with 20 mL of n-hexane.

5 the monobranched isomers and finally linear n-hexane.

6 n the solvents tetrahydrofuran, methanol, or n-hexane.

7 is found to be 22 times larger than in sole n-hexane.

8 lar organic liquids, such as cyclohexane and n-hexane.

9 using acetone as a modifier in CH2Cl2 or in n-hexane.

10 ht product of the metathesis of two moles of n-hexane.

11 ensemble of 1-hexanol aggregates solvated in n-hexane.

12 also higher than in the oils extracted with n-hexane.

13 30 degrees C and solvent mixture of acetone/n-hexane 1:3 (v/v) provided optimal conditions for extra

14 A mixture of acetone/n-hexane (1:1, v/v) was selected for accelerated solvent

15 PA in the gas phase and in various solvents (n-hexane, 1-chlorohexane, acetone, and water) were estab

16 face reactions of various C(6) hydrocarbons (n-hexane, 2-methylpentane, 3-methylpentane, and 1-hexene

17 A single n-hexane/2-propanol extract containing both types of com

18 ), time (1-60 min), percentage of acetone in n-hexane (25-75%, v/v) and solvent volume (10-30 ml) was

19 catalytic activity for hydroisomerization of n-hexane, a reaction requiring hydrogenation/dehydrogena

20 compounds were extracted simultaneously with n-hexane/acetone/ethanol (50/25/25, v/v/v).

21 AHs in the processed meats were extracted in n-hexane after hydrolysis with methanolic KOH.

22 nto the stationary phase is very small, both n-hexane and 1-pentanol partition strongly into and ther

23 96 K and in the presence of excess hydrogen, n-hexane and 3-methylpentane adsorbed molecularly on Pt(

24 excess hydrogen enhanced dehydrogenation of n-hexane and 3-methylpentane to form pi-allyl c-C(6)H(9)

25 ial nonpolar S3(FC) to long-lived (1.3 ns in n-hexane and 3.4 ns in acetonitrile) polar S1.

26 products of n-hexane isomerization (140 Torr n-hexane and 620 Torr H2 at 360 degrees C).

27 (Malvaceae) was extracted successively with n-hexane and chloroform.

28 The dehydrogenation of n-hexane and cycloalkanes giving n-hexene and cycloalken

29 ty in the wild type and Mar mutants (to both n-hexane and cyclohexane).

30 mutant resulted in loss of tolerance to both n-hexane and cyclohexane.

31 The solvents n-hexane and methyl n-butyl ketone are metabolized to th

32 that lower surface tension solvents, such as n-hexane and perfluoropentane, are applied.

33 a coli K-12 strains are normally tolerant to n-hexane and susceptible to cyclohexane.

34 butter sample was diluted and homogenised by n-hexane and Triton X-100, respectively.

35 st step, msLLE was conducted with 1.75 mL of n-hexane, and all of the extract was vaporized through a

36 t cavities in computer simulations of water, n-hexane, and n-dodecane under benchtop conditions shows

37 ficients for the alkane solutes for both the n-hexane- and 1-pentanol-swollen stationary phases, the

38 anol and trifluoroacetic acid (TFA)-modified n-hexane as the mobile phase.

39 tive concentration of PAHs while eliminating n-hexane by the FEDHS process.

40 Whereas saturation by n-hexane causes a decrease of the alcohol partition cont

41 owed the best performance using a mixture of n-hexane, chloroform, and dichloromethane (70 mL) for ex

42 were tested to isolate proteins, an acetone:n-hexane combination being the best protein precipitant.

43 and 30 bar in hybrid sorbents consisting of n-hexane confined in MIL-101 is found to be 22 times lar

44 D frequency shifts of solubilized deuterated n-hexane confirm that it resides in a dry, oil-like envi

45 In particular, significant n-hexane contamination ( approximately 0.4 ng/mL) occurr

46 rections for tunneling in both gas-phase and n-hexane environments.

47 as performed on silica gel with a mixture of n-hexane, ethyl acetate and ammonia.

48 d different solvents (CS2, toluene, acetone, n-hexane, ethyl acetate) are extensively studied as well

49 Analysis of the n-hexane extract by GC-MS led to the identification of t

50 ctane diterpenes 6-8, were isolated from the n-hexane extract of the marine sponge Svenzea flava coll

51 The soxhlet n-hexane extraction of these achenes produced a total oi

52 However, with n-hexane extracts with higher purity (mg ergosterol/g ex

53 amples and an additional defatting step with n-hexane for cheese, the matrix with the highest fat con

54 indicate an adsorption selectivity order of n-hexane > 2-methylpentane > 3-methylpentane > 2,3-dimet

55 Occupational exposure to solvents, including n-hexane, has been associated with acquired color vision

56 PH3)2L (W'-L, where L = H2, N2, C2H4, CO, or n-hexane) in an effort to confirm the infrared spectrosc

57 - or 3-methylpentane, as desired products of n-hexane isomerization (140 Torr n-hexane and 620 Torr H

58 n-Hexane isomerization rates were limited by isomerizati

59 d support-dependent catalytic selectivity in n-hexane isomerization.

60 n-Hexane levels above the method detection limit were, h

61 Samples were extracted using acetone/n-hexane mixtures at different ratios (1:3, 2:2 and 3:1,

62 es of atomic size in six molecular solvents: n-hexane, n-dodecane, n-undecyl alcohol, chloroform, car

63 terial, and the analytes included n-pentane, n-hexane, n-heptane, 1 -butanol, and 1-pentanol.

64 nterfacial adsorption effects for n-pentane, n-hexane, n-heptane, 1-butanol, and benzene solutes at i

65 e a new method for the analysis of alkanes ( n-hexane, n-heptane, n-octane, n-nonane, n-decane, n-und

66 e dissolution solvents used (tetrahydrofuran/n-hexane, n-hexane, or methanol) during photolysis.

67 ion solvents used (tetrahydrofuran/n-hexane, n-hexane, or methanol) during photolysis.

68 thylpentane, 3-methylpentane, n-pentane, and n-hexane produce methane in situ.

69 extraction efficiency of only 28% for BA in n-hexane, recirculative TSLLE resulted in a BA recovery

70 pite similar 1D-gel profiles, defatting with n-hexane resulted in significantly higher yields of crud

71 In contrast, in an isotropic n-hexane solution, there was little difference among the

72 components in plant seed oils extracted with n-hexane (Soxhlet method) and chloroform/methanol (Folch

73 actions from ABE and ABEa, ABEa-Ea-B (80% Ea/n-hexane sub-fraction from ABE-Ea) had the most potent i

74 The resulting quantification limits for n-hexane through n-decane ranged from 0.069 to 0.132 ng/

75 e to form a crystalline tBu(+) salt and with n-hexane to form an isolable hexyl carbocation salt.

76 for the catalytic conversion (reforming) of n-hexane to isomers.

77 For small hydrocarbons such as n-pentane or n-hexane, two guests enter the host, and they move freel

78 min, a solvent composition of 25% acetone in n-hexane (v/v) and solvent volume 40 ml.

79 hase composition: (i) a helium vapor, (ii) a n-hexane vapor, and (iii) a 1-pentanol-saturated helium

80 A polymer and PAHs, only the latter, and not n-hexane, was adsorbed by the sorbent.

81 action steps; 1-5) and two clean-up methods (n-hexane washing vs. low temperature fat precipitation)

82 on-sonicated counterpart (LLE-agitation) and n-hexane washing.

83 was used for rinsing, while acetonitrile and n-hexane were used as elution solvents.

84 lar (methanol, acetone, dichloromethane, and n-hexane) were selected to maximize the number of compou

85 ytic isomerization and dehydrocyclization of n-hexane, which are the important "reforming" reactions