Bibliografías temáticas / Organophosphorus (Toxicology) Chemistry

Literatura académica sobre el tema "Organophosphorus (Toxicology) Chemistry"

Autor: Grafiati
Publicado: 7 de septiembre de 2023

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Artículos de revistas sobre el tema "Organophosphorus (Toxicology) Chemistry"

1

Katritzky, Alan R., Julia V. Pervova, Petia A. Shipkova, Steven M. Allin, Michael Siskin y H. Dupont Durst. "Aqueous high‐temperature chemistry of organophosphorus compounds". Toxicological & Environmental Chemistry 59, n.º 1-4 (marzo de 1997): 219–38. http://dx.doi.org/10.1080/02772249709358438.

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Sevalkar, Murlidhar T., Vitthal Patil y Harischandra N. Katkar. "Zinc Chloride-Diphenylamine Reagent for Thin Layer Chromatographic Detection of Some Organophosphorus and Carbamate Insecticides". Journal of AOAC INTERNATIONAL 74, n.º 3 (1 de mayo de 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. y Murlidhar S. Shingare. "Thin-Layer Chromatographic Detection of Organophosphorus Insecticides Containing a Nitrophenyl Group". Journal of AOAC INTERNATIONAL 76, n.º 6 (1 de noviembre de 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 y B. K. Sharma. "Photodegradation of the organophosphorus herbicide “anilophos”". Toxicological & Environmental Chemistry 37, n.º 3-4 (febrero de 1993): 191–94. http://dx.doi.org/10.1080/02772249309357869.

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Sharma, B. K. y Navindu Gupta. "Photodegradation of the organophosphorus insecticide ‘Phorate’". Toxicological & Environmental Chemistry 41, n.º 3-4 (marzo de 1994): 249–54. http://dx.doi.org/10.1080/02772249409357980.

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Azlan, Nadiah Syafiqah Mohd, Sze Yee Wee, Nur Afifah Hanun Ismail, Hanisah Mohmad Nasir y Ahmad Zaharin Aris. "Organophosphorus Pesticide Multiresidues in Commercialized Asian Rice". Environmental Toxicology and Chemistry 39, n.º 10 (17 de agosto de 2020): 1908–17. http://dx.doi.org/10.1002/etc.4813.

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Tsuzuki, Manabu. "Thermodynamic estimation of vapor pressure for organophosphorus pesticides". Environmental Toxicology and Chemistry 19, n.º 7 (julio de 2000): 1717–26. http://dx.doi.org/10.1002/etc.5620190704.

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Sujatha, C. H. y J. Chacko. "Organophosphorus pesticide adsorption variability in diverse estuarine sediments". Toxicological & Environmental Chemistry 36, n.º 1-2 (julio de 1992): 65–73. http://dx.doi.org/10.1080/02772249209357828.

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Sengupta, S. K., O. P. Pandey, G. P. Rao y Priyanka Singh. "Efficacy of Organophosphorus Derivatives Containing Chalcones/Chalcone Semicarbazones Against Fungal Pathogens of Sugarcane". Metal-Based Drugs 8, n.º 5 (1 de enero de 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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Fröbe, Z., V. Drevenkar, B. Štengl y M. Juračić. "Sorption behaviour of some organophosphorus pesticides in natural sediments∗". Toxicological & Environmental Chemistry 19, n.º 1-2 (febrero de 1989): 69–82. http://dx.doi.org/10.1080/02772248909357333.

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Libros sobre el tema "Organophosphorus (Toxicology) Chemistry"

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

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3

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

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4

(Editor), Janice E. Chambers y 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) y Darren S. Baldwin (Editor), eds. Organic Phosphorus in the Environment (Cabi Publishing). CABI, 2005.

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Capítulos de libros sobre el tema "Organophosphorus (Toxicology) Chemistry"

1

Balali-Mood, Beeta. "Chemistry and Classification of OP Compounds". En 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 y Janice E. Chambers. "Chemistry of Organophosphorus Insecticides". En Handbook of Pesticide Toxicology, 913–17. Elsevier, 2001. http://dx.doi.org/10.1016/b978-012426260-7.50047-1.

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Chambers, Howard W., Edward C. Meek y Janice E. Chambers. "Chemistry of Organophosphorus Insecticides". En 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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