ライフサイエンスコーパス: isopropanol

1 d in silica-based extractions (guanidine and isopropanol).

2 formate salts as hydrogen donors in aqueous isopropanol.

3 nsfer hydrogenation of acetophenone in basic isopropanol.

4 cyclohexane molecules, but did reveal bound isopropanol.

5 n, VA cells were cultured in the presence of isopropanol.

6 nation rates were reduced from 3.04% for 70% isopropanol-1% iodine (control antiseptic) to 1.04% for

7 iodine (control antiseptic) to 1.04% for 70% isopropanol-1% iodine-5% DMSO (P < 0.01).

8 improved microscale synthesis of 2-tritiated isopropanol ([2-3H]iPrOH) and R-tritiated reduced beta-n

9 hest lipid removal (87%), followed by hexane/isopropanol (78%).

10 imethylformamide, 80% 5-hexene-1,2-diol, 80% isopropanol, 80% ethanol and 40% trifluoroethanol showed

11 tion under the coupling conditions, although isopropanol, a secondary alcohol, may serve as terminal

12 e., methanol, acetonitrile, isopropanol, and isopropanol-acetonitrile) and four liquid-liquid extract

13 HPLC and a solvent system containing hexane/isopropanol/acetonitrile/acetic acid (800/8/30/1, v/v) u

14 ed pyridine aggregation but had no effect on isopropanol aggregation.

15 reaction conditions, but in the presence of isopropanol, aldehydes 3a-3i are converted to an equival

16 from gut microbiota (formate, methanol, and isopropanol; all elevated).

17 res of 40% benzene or 40% cyclohexane in 50% isopropanol and 10% water showed no bound benzene or cyc

18 ward a broad array of substrates including n-isopropanol and beta-estradiol.

19 RNA is then recovered by precipitation with isopropanol and can be used for several applications.

20 g the molecules in organic solvents, such as isopropanol and dimethylsulfoxide or by enzymatic cleava

21 e reagents used for conventional extraction (isopropanol and guanadinium hydrochloride), which are po

22 SANS data showed that isopropanol and pyridine both form clusters in water res

23 de in water mixtures with methanol, ethanol, isopropanol and t-butyl alcohol.

24 Competition reactions with isopropanol and trimethyl(methallyl)silane are interpret

25 id of PCR inhibitors that are reagent-based (isopropanol) and sample-based (indigo dye), both of whic

26 butanol, acetonitrile, methanol, n-propanol, isopropanol, and isobutanol.

27 ation methods (i.e., methanol, acetonitrile, isopropanol, and isopropanol-acetonitrile) and four liqu

28 sters of methanol, ethanol, ethylene glycol, isopropanol, and propylene glycol are obtained with grea

29 tion, PLA conditioning of the cartridge with isopropanol, and solvent volume introduced into the rese

30 um were recovered by means of formaldehyde-, isopropanol- and ethanol-based extractions and analyzed

31 Additionally, isopropanol appeared to be the most straightforward and

32 e used as substrates; N-benzoyloxyamines and isopropanol are employed as the amine source (oxidant) a

33 EP under identical conditions, but employing isopropanol as a hydrogen donor.

34 latin can be used for such analyses by using isopropanol as precipitating reagent.

35 Employing isopropanol as terminal reductant, exposure of allyl ace

36 transfer hydrogenation conditions employing isopropanol as terminal reductant, isoprene couples to a

37 -2j under the same conditions, but employing isopropanol as the terminal reductant.

38 opha enabled production of the fusel alcohol isopropanol at up to 216 mg/L, the highest bioelectroche

39 point using solid carbon dioxide (CO2) in an isopropanol bath.

40 The metabolism of isopropanol by VA cells resulted in very little reductio

41 Increasing isopropanol concentration above 40% resulted in a decrea

42 enase and trypsin inhibitors, as compared to isopropanol containing solvents (P<0.05).

43 the non-defatted flour and those defatted by isopropanol containing solvents throughout the storage (

44 low dielectric solvents (acetone, methanol, isopropanol, DMF, DMSO, chloroform, and CCl(4)).

45 trolysis studies confirm that the product of isopropanol electrooxidation is acetone, generated with

46 t extraction of soybean seed powder with 40% isopropanol enriches lower abundance proteins and is a s

47 out fluid or in large molecule fluids (e.g., isopropanol, ethanol, or fluorinert), the high-pressure

48 Bioactivity guided isolation of rhizome isopropanol extract led to the identification by HPLC an

49 We investigated whether isopropanol extraction could facilitate resolution of th

50 Results on FA composition using the hexane/isopropanol extraction method were the same in terms of

51 ntaminants were removed by phenol-chloroform-isopropanol extraction prior to DNA precipitation.

52 ction procedure were clearly seen in the 40% isopropanol extracts.

53 lamide gels by pretreating the gels with 50% isopropanol followed by distilled water treatment.

54 The samples grafted in isopropanol gave colors and lambdamax intermediate betwe

55 Suspensions of acetone- and isopropanol-grown R. rhodochrous readily metabolized ace

56 tion producing longer-range structuring than isopropanol in 3 m solutions.

57 ectrometry, we optimized solvent conditions: isopropanol in a triethylamine/hexafluoroisopropanol mix

58 and 2 are active for the electrooxidation of isopropanol in the presence of strong base (potassium t-

59 ies of the GO doped isotropic media, such as isopropanol IPA, were observed to be much lower than the

60 turing (aggregation) of aqueous solutions of isopropanol (IPA) and pyridine and the effect on structu

61 ic materials common in bioparticle analysis: isopropanol (IPA) and sucrose.

62 l, ethylene glycol (EG), ethyl acetate (EA), isopropanol (IPA), propylene glycol (PG), polyethylene g

63 solvents including tetrahydrofuran (THF) and isopropanol (iPrOH).

64 eover, selective tandem double alkylation of isopropanol is achieved by sequential addition of differ

65 ile alcohols, such as methanol, ethanol, and isopropanol lead to a significant reduction in sodium io

66 Identical products are obtained upon isopropanol-mediated transfer hydrogenation of donor-acc

67 ne glycol, dimethylsilanediol, formaldehyde, isopropanol, methanol, methylethyl ketone, methylsulfone

68 rried out upon its immobilization from water-isopropanol mixtures with the high (90%) content of orga

69 chiral SFC (Chiralcel OJ-3 and Chiralpak IB, isopropanol or ethanol with 25 mM isobutylamine/carbon d

70 organometallic catalysts most often rely on isopropanol or formate to generate the reactive hydride

71 thod and liquid-solid extraction with hexane/isopropanol or with hexane/acetone were investigated, as

72 urnover frequencies of 3.2 and 4.8 s(-1) for isopropanol oxidation are achieved with 1 and 2, respect

73 Water substantially promotes isopropanol oxidation in the liquid phase.

74 dox changes, but the metabolic by-product of isopropanol oxidation is acetone.

75 nm and use them as model catalysts to study isopropanol oxidation to acetone in both the liquid and

76 As)--N-ethanol palythine (= asterina-330), N-isopropanol palythine (= aplysiapalythine A), and N-ethy

77 (i) Silica-assisted ethanol/isopropanol precipitation ensures reproducible and effic

78 hat lipid profiling greatly benefits from an isopropanol precipitation in terms of simplicity, protei

79 These results demonstrate that isopropanol precipitation is an excellent sample prepara

80 Isopropanol precipitation is not limited to untargeted p

81 Chaotropic lysis and isopropanol precipitation were used to extract RNA from

82 The oxidation of isopropanol results in similar redox changes, but the me

83 Trapping studies using d8-isopropanol showed deuterium incorporation in 5-chloro-2

84 0%, 20%, 30%, 40%, 50%, 60%, 70% and 80%) of isopropanol showed that greater than 30% isopropanol was

85 of WGO and PGO delivered in organic solvent (isopropanol) showed dose-dependent antimicrobial activit

86 ze, i.e., methanol, ethanol, n-propanol, and isopropanol, showing that fine control over the thermal

87 gated the effects of post-column addition of isopropanol solutions of formaldehyde, 2,2-dimethylpropa

88 The dichloromethane/isopropanol solvent has been identified as an optimal sp

89 -helix forms on addition of small amounts of isopropanol to the aqueous subphase, and appears to be a

90 atalyzed a hydride transfer from C-2-labeled isopropanol to the re face of oxidized nicotinamide aden

91 rystallographic experiments (low pH and 26 % isopropanol), two symmetrically related monomers form a

92 r the transfer hydrogenation of ketones with isopropanol under ambient conditions.

93 In the presence of isopropanol under otherwise identical conditions, aldehy

94 of isopropanol showed that greater than 30% isopropanol was suitable for preferential enrichment of

95 Efficacy in defatting was higher than when isopropanol was used.

96 nging the dielectric environment from air to isopropanol, we observe a 25% reduction in the transport

97 teractions involving the aliphatic groups of isopropanol were unaffected by GdmCl, indicating that th

98 milar extent by propofol, phenylethanol, and isopropanol when added at anesthetic concentrations, but

99 was achieved by treating the microarray with isopropanol, which prevents nucleic acids from dissolvin

100 Isopropanol with 1.0% trichloroacetic acid was found to

101 loromethane, and methyl-tert butyl ether and isopropanol with hexane).