ライフサイエンスコーパス: chemical warfare agent

1 phorous chemicals including insecticides and chemical warfare agents.

2 rable characteristics for the destruction of chemical warfare agents.

3 xification of toxic industrial chemicals and chemical warfare agents.

4 xification of organophosphate pesticides and chemical warfare agents.

5 by selected organophosphorus pesticides and chemical warfare agents.

6 counterterrorism responses to biological and chemical warfare agents.

7 oxification of agricultural insecticides and chemical warfare agents.

8 on of organophosphate-based insecticides and chemical warfare agents.

9 off from sites that produce the compounds as chemical warfare agents.

10 In addition, these toxins are suspected chemical warfare agents.

11 and used in the catalytic decontamination of chemical warfare agents.

12 drome" among veterans potentially exposed to chemical warfare agents; 2) compare the findings of fact

13 Organophosphorus (OP) insecticides and chemical warfare agents act primarily by inhibiting acet

14 hydrocarbons and the high-speed analysis of chemical warfare agent and explosive markers.

15 The investigated compounds include an intact chemical warfare agent and structurally related molecule

16 luoridates, which are common constituents of chemical warfare agents and agricultural pesticides.

17 screening, identification, and validation of chemical warfare agents and other small-molecule analyte

18 nger countermeasure against organophosphorus chemical warfare agents and pesticides is warranted.

19 A wide range of chemical warfare agents and their simulants are catalyti

20 espread use for the screening of explosives, chemical warfare agents, and illicit drugs.

21 Most of the organophosphate chemical warfare agents are a mixture of two stereoisome

22 for the in-the-field detection of traces of chemical warfare agents as well as to differentiate betw

23 veterans who had witnessed the demolition of chemical warfare agents at the Khamisiyah site in Iraq h

24 f organophosphates, including pesticides and chemical warfare agents, at rates approaching the diffus

25 Chemical warfare agents containing phosphonate ester bon

26 ection limits is observed in the analysis of chemical warfare agent (CWA) degradation products in env

27 ped to determine oxidation products of three chemical warfare agent (CWA) related phenylarsenic compo

28 ht mass spectrometer (IM(tof)MS) to detect a chemical warfare agent (CWA) simulant from aerosol sampl

29 ed identification of single particles of the chemical warfare agent (CWA) simulants at each laser flu

30 ight mass spectrometer (IM(tof)MS) to detect chemical warfare agent (CWA) simulants from both aqueous

31 Aerosolized chemical warfare agent (CWA) simulants trimethyl phospha

32 Detection of chemical warfare agent (CWA) simulants, illicit drugs, a

33 Ion mobility spectra of chemical warfare agent (CWA) stimulant dimethyl methylph

34 f catalytic oxidative decontamination of the chemical warfare agent (CWA) sulfur mustard (HD, bis(2-c

35 vice when using fixed sampling times for the chemical warfare agent (CWA) surrogate compound, diisopr

36 ironment, are examined as decontaminants for chemical warfare agents (CWA).

37 The threat associated with chemical warfare agents (CWAs) motivates the development

38 ions (3-30%) efficiently decomposes adsorbed chemical warfare agents (CWAs) on microporous activated

39 avenues for the mitigation of the effects of chemical warfare agents (CWAs), including sensing, catal

40 ion of a CE-based method for the analysis of chemical warfare agent degradation products in agent neu

41 hods have been developed for the analysis of chemical warfare agent degradation products in reaction

42 ng of pharmaceutical compounds, detection of chemical warfare agents, environmental hygiene technolog

43 ger group of veterans potentially exposed to chemical warfare agents; however, veterans who had witne

44 Recently, a new class of reactivators of chemical warfare agent inhibited acetylcholinesterase (A

45 Lewisite is a potent arsenic-based chemical warfare agent known to induce painful cutaneous

46 by several organophosphorus (OP) pesticides, chemical warfare agents, lubricants, and plasticizers, l

47 derstanding the hydrolysis of the very toxic chemical warfare agent mustard (bis(2-chloroethyl)sulfid

48 widely utilized insecticide paraoxon and the chemical warfare agent sarin.

49 tection for the trace analysis in air of the chemical warfare agent simulant methyl salicylate (1.24

50 mechanism of adsorption and decomposition of chemical warfare agent simulants on Zr-based MOFs open n

51 Using a set of chemical warfare agent simulants with nominally the same

52 diacetylmorphine), organic salts, peptides, chemical warfare agent simulants, and other small organi

53 Data are given for chemical warfare agent simulants, methyl salicylate, and

54 specificity for NPPMP, the analogue for the chemical warfare agent soman.

55 on the capture and catalytic degradation of chemical warfare agents such as sarin and sulfur mustard

56 Incorporation of the chemical warfare agent sulfur mustard (SM) produces a co

57 important precursors of the extremely toxic chemical warfare agent sulfur mustard and classified, re

58 numerous positive and negative ions with VX chemical warfare agent surrogates representing the amine

59 Among the chemical warfare agents, the extremely toxic nerve agent

60 rganophosphates have been adapted for use as chemical warfare agents; the most well-known are GA, GB,

61 ents to organophosphorus (OP) pesticides and chemical warfare agents; therefore, they warrant explora

62 low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives

63 tremely toxic and environmentally persistent chemical warfare agent VX (O-ethyl S-2-(diisopropylamino

64 or demeton S (P-S bond), an analogue for the chemical warfare agent VX.

65 Chemical warfare agents were demolished by US soldiers a

66 omise for monitoring degradation products of chemical warfare agents, with advantages of speed/warnin