ライフサイエンスコーパス: trinitrotoluene

1 4,6-trinitrophenylmethylnitramine), and TNT (trinitrotoluene).

2 tranitro-1,3,5,7-Tetrazocine)) or TNT (2,4,6-trinitrotoluene).

3 l enterotoxin B) and a small molecule (2,4,6-trinitrotoluene).

4 ed in a plant species to sense environmental trinitrotoluene.

5 Aromatic explosives such as 2,4,6-trinitrotoluene (2,4,6-TNT) are more effective quenchers

6 ses each of the munitions constituents 2,4,6-trinitrotoluene, 2,4-dinitrotoluene, 2,6-dinitrotoluene,

7 trazine and azoxystrobin, and the explosives trinitrotoluene and dinitroglycerin in under 20 s.

8 velocity of 7.20 0.27 km s(-1) comparable to trinitrotoluene and hexanitrostilbene.

9 an MICP material for the detection of 2,4,6-trinitrotoluene and related nitroaromatic compounds.

10 cation of enzymes capable of degrading 2,4,6-trinitrotoluene and this still remains elusive, although

11 dynamic voltammograms of nitrobenzene, 2,4,6-trinitrotoluene, and hexahydro-1,3,5-trinitro-1,3,5-tria

12 -nitrotoluene, 2,4-dinitrotoluene, and 2,4,6-trinitrotoluene, as well as the peroxide-based explosive

13 of 1 mM glycerol trinitrate (GTN) or 0.05 mM trinitrotoluene, at concentrations that inhibited germin

14 dual nitroaromatic explosives (such as 2,4,6-trinitrotoluene) can be easily detected in amounts as lo

15 haracterizing, plant genes involved in 2,4,6-trinitrotoluene detoxification and the biochemical pathw

16 Results for trinitrotoluene, dinitrotoluenes, and nitrotoluenes are

17 sed to construct soluble receptors that bind trinitrotoluene, l-lactate or serotonin with high select

18 gene expression in response to extracellular trinitrotoluene or l-lactate.

19 efinition of the polymorphic nature of 2,4,6-trinitrotoluene precipitated from solution.

20 unition compounds (MC), including TNT: 2,4,6-trinitrotoluene, RDX: 1,3,5-trinitro-1,3,5-triazinane, a

21 n and tissue residue of two chemicals, 2,4,6-trinitrotoluene (TNT) and 1,3,5-trinitro-1,3,5-triazacyc

22 The trinitroaromatic explosives, 2,4,6-trinitrotoluene (TNT) and 1,3,5-trinitrobenzene (TNB), a

23 this study, the alkaline hydrolysis of 2,4,6-trinitrotoluene (TNT) and 2,4-dinitroanisole (DNAN) was

24 Trace vapours of the explosives 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (DNT) intro

25 security concerns, including the explosives trinitrotoluene (TNT) and ammonium nitrate.

26 Utilizing phage display techniques against trinitrotoluene (TNT) and dinitrotoluene (DNT) targets,

27 The principle is exemplified via trinitrotoluene (TNT) and dinitrotoluene (DNT) with inhe

28 miluminescence enzyme immunoassays for 2,4,6-trinitrotoluene (TNT) and pentaerythritol tetranitrate (

29 ne coated with antibodies specific for 2,4,6-trinitrotoluene (TNT) and the other specific for hexahyd

30 s) and characterized biodegradation of 2,4,6-trinitrotoluene (TNT) and two dinitrotoluene isomers (2,

31 em to characterize PC reactivity using 2,4,6-trinitrotoluene (TNT) as a model contaminant and several

32 hase marker compounds of the explosive 2,4,6-trinitrotoluene (TNT) at sub-parts-per-billion (<ppb) co

33 nd characterization of an amperometric 2,4,6-trinitrotoluene (TNT) biosensor based on the surface imm

34 e report high-sensitivity detection of 2,4,6-trinitrotoluene (TNT) by using laser photoacoustic spect

35 ree detection of explosive molecules such as trinitrotoluene (TNT) down to 10(-10)M in concentration

36 is roots and assess their responses to 2,4,6-trinitrotoluene (TNT) exposure.

37 for rapid preconcentration and extraction of trinitrotoluene (TNT) for electrochemical analysis and d

38 ,3,5-trinitro-1,3,5-triazine (RDX) and 2,4,6-trinitrotoluene (TNT) from poly(tetrafluoroethylene) (PT

39 erned array of antibodies specific for 2,4,6-trinitrotoluene (TNT) immobilized onto the surface of a

40 e spectroscopy (EIS) is used to detect 2,4,6-trinitrotoluene (TNT) in a novel sandwiched structure wh

41 he specific detection of the explosive 2,4,6-trinitrotoluene (TNT) in aqueous environments.

42 or detection of the explosive compound 2,4,6-trinitrotoluene (TNT) in aqueous solution was developed

43 ct and quantify the explosive compound 2,4,6-trinitrotoluene (TNT) in aqueous solutions is demonstrat

44 t of 2 x 10(-12) mol (i.e., 2 pmol) of 2,4,6-trinitrotoluene (TNT) in connection with 47 nL of inject

45 asing use of DNAN as a replacement for 2,4,6-trinitrotoluene (TNT) in insensitive explosive formulati

46 re, our results indicated that it can detect trinitrotoluene (TNT) in liquid at a concentration as lo

47 or for the detection of the explosive, 2,4,6-trinitrotoluene (TNT) in seawater using a reversed-displ

48 X), pentaerythritol tetranitrate (PETN), and trinitrotoluene (TNT) in their crystalline forms and alu

49 acticality of this device by detecting 2,4,6-trinitrotoluene (TNT) in water at sub-mg/L detection lim

50 The explosive 2,4,6-trinitrotoluene (TNT) is a highly toxic and persistent e

51 The explosive 2,4,6-trinitrotoluene (TNT) is a major worldwide military poll

52 The explosive 2,4,6-trinitrotoluene (TNT) is a significant, global environme

53 Trinitrotoluene (TNT) is a widely used explosive in land

54 e, selective and portable detection of 2,4,6-trinitrotoluene (TNT) is in high demand for public safet

55 2,4,6-Trinitrotoluene (TNT) is one of the most recalcitrant an

56 The toxic pollutant 2,4,6-trinitrotoluene (TNT) is recalcitrant to degradation in

57 ndence in the detection sensitivity of 2,4,6 trinitrotoluene (TNT) on the reduced electric field (E/N

58 Higher trinitrotoluene (TNT) quantity and closer explosion caus

59 explosive detection is reported using 2,4,6-trinitrotoluene (TNT) specific aptamer and antibodies ta

60 the selective detection of trace amounts of trinitrotoluene (TNT) still remains a big challenge for

61 e) and 1,3,5-trimethylbenzene (TMB) (a 2,4,6-trinitrotoluene (TNT) surrogate) in a mixture of N(2) an

62 The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated using films of va

63 tra from 1000 single particles each of 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitro-1,3,5-triazinane (

64 including 2,4,6-trinitrophenol (TNP), 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitrobenzene (TNB), and

65 against three widely used explosives, 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitroperhydro-1,3,5-tria

66 It was used to identify the explosives 2,4,6-trinitrotoluene (TNT), 2,4,6-trinitrophenyl-N-methylnitr

67 ogates including nitroaromatics [NACs; 2,4,6-trinitrotoluene (TNT), 2,4-dinitroanisole (DNAN), 2-amin

68 on of nitroaromatic compounds, such as 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), 2,6

69 using newly measured kinetic data for 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), and

70 ysis of three nitroaromatic compounds: 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), and 2,4

71 l detection of nitroaromatic compounds 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), and fen

72 rinitroper-hydro-1,3,5-triazine (RDX), 2,4,6-trinitrotoluene (TNT), 2-amino-4,6-dinitrotoluene (ADNT)

73 s for multiple plant natural products, 2,4,6-trinitrotoluene (TNT), and "forever" per- and polyfluoro

74 (AOC), 2 mm metolachlor (MOC), 0.6 mm 2,4,6-trinitrotoluene (TNT), and 0.3 mm hexahydro-1,3,5-trinit

75 .4-dichlorophenoxyacetic acid (2,4-D), 2,4,6-trinitrotoluene (TNT), and 1,3,5-trinitroperhydro-1,3,5-

76 esulting in the detection of 0.6 ng of 2,4,6-trinitrotoluene (TNT), and low explosives (several smoke

77 enzene (NB), 2,4-dinitrotoluene (DNT), 2,4,6-trinitrotoluene (TNT), and picric acid (PA), has been ex

78 ecause RDX is 10(3) less volatile than 1,3,5-trinitrotoluene (TNT), corresponding to a parts-per-tril

79 micals [pentaerythritol tetranitrate (PETN), trinitrotoluene (TNT), cyclo-1,3,5-trimethylenetrinitram

80 The generation of trace 2,4,6-trinitrotoluene (TNT), cyclotrimethylenetrinitramine (RD

81 ntrations of 1 ppm of trinitrobenzene (TNB), trinitrotoluene (TNT), dinitrobenzene (DNB), tetryl, and

82 ) at 100-fold ratios nor nitro-explosives of trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-tr

83 lective technique for the detection of 2,4,6-trinitrotoluene (TNT), hexanitrostillbene (HNS), and 2,4

84 on of a model nitroaromatic explosive, 2,4,6-trinitrotoluene (TNT), is presented as a prime example.

85 ,4-DNT), 2,6-dinitrotoluene (2,6-DNT), 2,4,6-trinitrotoluene (TNT), nitroglycerin (NG), 1,3,5-trinitr

86 -tetranitro-1,3,5,7-tetrazocine (HMX), 2,4,6-trinitrotoluene (TNT), Pentaerythritol tetranitrate (PET

87 different analytes, including the explosives trinitrotoluene (TNT), tetryl, and RDX, various explosiv

88 ermore, sensors composed of phage displaying trinitrotoluene (TNT)-binding peptide motifs identified

89 sensitivity of detecting the explosive 2,4,6-trinitrotoluene (TNT).

90 NACs), displaying superior detection toward trinitrotoluene (TNT).

91 ate (PETN) and significantly exceeds that of trinitrotoluene (TNT).

92 c response of Daphnia magna to the energetic trinitrotoluene (TNT).

93 tiate NAD(P)H-dependent denitration of 2,4,6-trinitrotoluene (TNT).

94 One such compound is the explosive 2,4,6-trinitrotoluene (TNT).

95 hexen-1-one but did not readily reduce 2,4,6-trinitrotoluene (TNT).

96 active catalysts for the reduction of 2,4,6-trinitrotoluene to 2,4,6-triaminotoluene and subsequent

97 a series of dinitrotoluenes, dinitrobenzene, trinitrotoluene, trinitrobenzene, two aminodinitrotoluen

98 build new sensors for the detection of 2,4,6-trinitrotoluene via nitroaromatic markers is shown.

99 or 60 repetitive measurements of 5 ppm 2,4,6-trinitrotoluene (vs RSD of 10.8% at the thick-film carbo