Relevant bibliographies by topics / Organophosphorus (Toxicology) Chemistry

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Academic literature on the topic 'Organophosphorus (Toxicology) Chemistry'

Author: Grafiati
Published: 7 September 2023

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Journal articles on the topic "Organophosphorus (Toxicology) Chemistry"

1

Katritzky, Alan R., Julia V. Pervova, Petia A. Shipkova, Steven M. Allin, Michael Siskin, and H. Dupont Durst. "Aqueous high‐temperature chemistry of organophosphorus compounds." Toxicological & Environmental Chemistry 59, no. 1-4 (March 1997): 219–38. http://dx.doi.org/10.1080/02772249709358438.

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2

Sevalkar, Murlidhar T., Vitthal Patil, and Harischandra N. Katkar. "Zinc Chloride-Diphenylamine Reagent for Thin Layer Chromatographic Detection of Some Organophosphorus and Carbamate Insecticides." Journal of AOAC INTERNATIONAL 74, no. 3 (May 1, 1991): 545–46. http://dx.doi.org/10.1093/jaoac/74.3.545.

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Abstract Zinc chlorlde-diphenylamlne reagent, whose use has been reported for the detection of organochlorine insecticides by thin layer chromatography, was further studied for its ability to detect the organophosphorus insecticides phorate, phosphamldon, DDVP, and phosalone and the carbamate Insecticides carbaryl and aldicarb. These Insecticides give Intense blue-green spots with this reagent. The procedure can be applied to the detection of the insecticides in biological materials and thus has a potential use in forensic toxicology
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3

Patil, Vitthal B., and Murlidhar S. Shingare. "Thin-Layer Chromatographic Detection of Organophosphorus Insecticides Containing a Nitrophenyl Group." Journal of AOAC INTERNATIONAL 76, no. 6 (November 1, 1993): 1394–95. http://dx.doi.org/10.1093/jaoac/76.6.1394.

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Abstract A Griess reaction that has been used to detect organic compounds containing an aromatic amino group was used to detect organophosphorus compounds containing a nitrophenyl group, such as ethyl parathion, methyl parathion, and fenitrothion. On reduction with stannous chloride in HCI–water (1 + 1), these compounds give respective amino derivatives, which are further diazotized and coupled with 1-naphthylamine to give intense pink–orange spots. This reagent also gives a bluish to violet spot with p-nitrophenol, a metabolite of fenitrothion. The procedure can be used to detect these insecticides in biological materials in forensic toxicology.
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4

Gupta, Navindu, P. Dureja, and B. K. Sharma. "Photodegradation of the organophosphorus herbicide “anilophos”." Toxicological & Environmental Chemistry 37, no. 3-4 (February 1993): 191–94. http://dx.doi.org/10.1080/02772249309357869.

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Sharma, B. K., and Navindu Gupta. "Photodegradation of the organophosphorus insecticide ‘Phorate’." Toxicological & Environmental Chemistry 41, no. 3-4 (March 1994): 249–54. http://dx.doi.org/10.1080/02772249409357980.

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6

Azlan, Nadiah Syafiqah Mohd, Sze Yee Wee, Nur Afifah Hanun Ismail, Hanisah Mohmad Nasir, and Ahmad Zaharin Aris. "Organophosphorus Pesticide Multiresidues in Commercialized Asian Rice." Environmental Toxicology and Chemistry 39, no. 10 (August 17, 2020): 1908–17. http://dx.doi.org/10.1002/etc.4813.

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7

Tsuzuki, Manabu. "Thermodynamic estimation of vapor pressure for organophosphorus pesticides." Environmental Toxicology and Chemistry 19, no. 7 (July 2000): 1717–26. http://dx.doi.org/10.1002/etc.5620190704.

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8

Sujatha, C. H., and J. Chacko. "Organophosphorus pesticide adsorption variability in diverse estuarine sediments." Toxicological & Environmental Chemistry 36, no. 1-2 (July 1992): 65–73. http://dx.doi.org/10.1080/02772249209357828.

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9

Sengupta, S. K., O. P. Pandey, G. P. Rao, and Priyanka Singh. "Efficacy of Organophosphorus Derivatives Containing Chalcones/Chalcone Semicarbazones Against Fungal Pathogens of Sugarcane." Metal-Based Drugs 8, no. 5 (January 1, 2002): 293–302. http://dx.doi.org/10.1155/mbd.2002.293.

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Ten newly synthesized organophosphorus derivatives containing substituted chalcones and substituted chalcone semicarbazones were tested for their antifungal efficacy against Colletotrichum falcatum, Fusarium oxysporum, Curvularia pallescens (all sugarcane pathogens). The O,O-diethylphosphate derivatives containing 2-chlorochalcone and 2-chlorochalcone semicarbazone exhibited 70-85% mycelial inhibition against all the test fungi at 1000 ppm. The screening results were correlated with structural features of the tested compounds.
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10

Fröbe, Z., V. Drevenkar, B. Štengl, and M. Juračić. "Sorption behaviour of some organophosphorus pesticides in natural sediments∗." Toxicological & Environmental Chemistry 19, no. 1-2 (February 1989): 69–82. http://dx.doi.org/10.1080/02772248909357333.

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Books on the topic "Organophosphorus (Toxicology) Chemistry"

1

Andriyanova, Mariya, Aslanli Aslanli, Nataliya Basova, Viktor Bykov, Sergey Varfolomeev, Konstantin Gorbunov, Valentin Gorelenkov, et al. ORGANOPHOSPHORUS NEUROTOXINS. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/02026-5.

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The collective monograph is devoted to discussing the history of creation, studying the properties, neutralizing and using organophosphorus neurotoxins, which include chemical warfare agents, agricultural crop protection chemical agents (herbicides and insecticides) and medicines. The monograph summarizes the results of current scientific research and new prospects for the development of this field of knowledge in the 21st century, including the use of modern physicochemical methods for experimental study and theoretical analysis of biocatalysis and its mechanisms based on molecular modeling with supercomputer power. The book is intended for specialists who are interested in the current state of research in the field of organophosphorus neurotoxins. The monograph will be useful for students, graduate students, researchers specializing in the field of physical chemistry, physicochemical biology, chemical enzymology, toxicology, biochemistry, molecular biology and genetics, biotechnology, nanotechnology and biomedicine.
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2

E, Chambers Janice, and Levi Patricia E, eds. Organophosphates: Chemistry, fate, and effects. San Diego: Academic Press, 1992.

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3

(Editor), Janice E. Chambers, and Patricia E. Levi (Editor), eds. Organophosphates: Chemistry, Fate, and Effects. Academic Press, 1992.

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4

(Editor), Janice E. Chambers, and Patricia E. Levi (Editor), eds. Organophosphates: Chemistry, Fate, and Effects. Academic Press, 1992.

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5

(Editor), Benjamin L. Turner, Emmanuel Frossard (Editor), and Darren S. Baldwin (Editor), eds. Organic Phosphorus in the Environment (Cabi Publishing). CABI, 2005.

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Book chapters on the topic "Organophosphorus (Toxicology) Chemistry"

1

Balali-Mood, Beeta. "Chemistry and Classification of OP Compounds." In Basic and Clinical Toxicology of Organophosphorus Compounds, 1–23. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-5625-3_1.

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2

Chambers, Howard W., J. Scott Boone, Russell L. Carr, and Janice E. Chambers. "Chemistry of Organophosphorus Insecticides." In Handbook of Pesticide Toxicology, 913–17. Elsevier, 2001. http://dx.doi.org/10.1016/b978-012426260-7.50047-1.

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3

Chambers, Howard W., Edward C. Meek, and Janice E. Chambers. "Chemistry of Organophosphorus Insecticides." In Hayes' Handbook of Pesticide Toxicology, 1395–98. Elsevier, 2010. http://dx.doi.org/10.1016/b978-0-12-374367-1.00064-1.

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You might also be interested in the extended bibliographies on the topic 'Organophosphorus (Toxicology) Chemistry' for particular source types:
Journal articles
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