• The Korean Journal of Pesticide Science
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• v.14 no.2
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• pp.170-174
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• 2010

The acaricidal activity of cyenopyrafen on the tea red spider mite, Tetranychus kanzawai was evaluated in laboratory and field studies. In the laboratory, cyenopyrafen was highly effective against egg, larva, protonymph and adult female of T. kanzawai. In surviving adult females of T. kanzawai exposed to cyenopyrafen, we observed significant reduction in reproduction and no egg hatch. Effectiveness of cyenopyrafen against adult female of T. kanzawai on bean leaves was lasted for 15 days at treatments of 125 and 83.3 ppm. In a field study, cyenopyrafen exhibited excellent activity to mixed developmental stages of T. kanzawai. Based on the results, cyenopyrafen could be used for the control of T. kanzawai and treatment of this acaricide at 83.3 ppm was recommended as the field rate.

• Journal of Microbiology and Biotechnology
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• v.17 no.8
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• pp.1394-1398
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• 2007

Acaricidal activity of the active constituent derived from Pyrus ussuriensis fruits against Dermatophagoides farinae and D. pteronyssinus was examined and compared with that of the commercial benzyl benzoate. The $LD_{50}$ value of the ethyl acetate fraction obtained from the aqueous extract of P. ussuriensis fruits was 9.51 and $8.59{\mu}g/cm^3$ against D. farinae and D. pteronyssinus, respectively. The active constituent was identified as quinone by spectroscopic analyses. On the basis of $LD_{50}$ values with quinone and its congeners, the compound most toxic against D. farinae was quinone ($1.19{\mu}g/cm^3$), followed by quinaldine (1.46), benzyl benzoate (9.32), 4-quinolinol (86.55), quinine (89.16), and 2-quinolinol (91.13). Against D. pteronyssinus, these were quinone ($1.02{\mu}g/cm^3$), followed by quinaldine (1.29), benzyl benzoate (8.54), 4-quinolinol (78.63), quinine (82.33), and 2-quinolinol (86.24). These results indicate that the acaricidal activity of the aqueous extracts can be mostly attributed to quinone. Quinone was about 7.8 and 8.4 times more toxic than benzyl benzoate against D. farinae and D. pteronyssinus. Additionally, quinaldine was about 6.4 and 6.6 times more toxic than benzyl benzoate against D. farinae and D. pteronyssinus, respectively. Furthermore, the skin color of the dust mites was changed from colorless-transparent to dark brown-black by the treatment of quinone. These results indicate that quinone can be very useful as potential control agents, lead compounds, or the indicator of house dust mites.

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2001.11a
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• pp.151-151
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• 2001

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2001.11a
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• pp.150-150
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• 2001

• 한국생물공학회:학술대회논문집
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• 2005.10a
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• pp.528-529
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• 2005

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2002.05a
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• pp.110-110
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• 2002

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2003.10a
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• pp.175-175
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• 2003

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2003.10a
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• pp.81-81
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• 2003

• Food Science and Biotechnology
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• v.14 no.1
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• pp.73-76
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• 2005

The acaricidal activities of 12 commercial constituents derived from Eugenia caryophyllata leaf oils against Dermatophagoides farinae, D. pteronyssinus and Tyrophagus putrescentiae adults were examined using an impregnated fabric disk application and compared with that of the commercial benzyl benzoate as synthetic acaricide. On the basis of $LD_{50}$ values, the most toxic compound was methyl eugenol ($4.13\;{\mu}g/cm^2$), followed by methyl isoeugenol ($4.19\;{\mu}g/cm^2$), isoeugenol ($4.29\;{\mu}g/cm^2$), eugenol ($4.94\;{\mu}g/cm^2$), and acetyl eugenol ($13.91\;{\mu}g/cm^2$) against D. farinae. In the case of D. pteronyssinus, isoeugenol ($2.93\;{\mu}g/cm^2$) was the most toxic, followed by methyl isoeugenol ($3.28\;{\mu}g/cm^2$), methyl eugenol ($3.87\;{\mu}g/cm^2$), eugenol ($3.92\;{\mu}g/cm^2$), and acetyl eugenol ($7.21\;{\mu}g/cm^2$). These results suggest that D. pteronyssinus may be controlled more effectively by the application of eugenol congeners than D. farinae. In comparison with synthetic acaricides, the acaricidal activities of eugenol, isoeugenol, methyl eugenol, and methyl isoeugenol were about 1.9-2.2 times more toxic than benzyl benzoate. Furthermore, the most toxic constituent against T. putrescentiae was exhibited on eugenol ($10.11\;{\mu}g/cm^2$), followed by methyl eugenol ($38.67\;{\mu}g/cm^2$) and acetyl eugenol ($70.09\;{\mu}g/cm^2$), but no activity was observed for isoeugenol and methyl isoeugenol. The results suggested that eugenol congeners may be useful as a new source for selective control of house dust mites and stored food mites.

• Applied Biological Chemistry
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• v.31 no.2
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• pp.193-199
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• 1988

This study was conducted to investigate the possibility of emulsifiable concentrate(EC) development and the stability and acaricidal activity of the formulated emulsifiable concentrate. Cyhexatin could be formulated into 9% EC by using phenol as a cosolvent and E-ASC as an emulsifier. Cyhexatin EC was stable in 0.5% moisture content, pH 4.5 and 7, but it was unstable in more than 1% moisture content and the alkaline condition of pH 9.5. The emulsion of cyhexatin EC was unstable in hard water of pH 10. The acaricidal activity of 500 fold of 9% EC was shown to be as good as that of 27% wp of 1500 fold.