Academic literature on the topic 'Thiodiglycol'

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Journal articles on the topic "Thiodiglycol"

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Samuilov, A. Ya, E. I. Galeeva, A. V. Kulikov, I. N. Bakirova, and Ya D. Samuilov. "Thiodiglycol-based oligomers." Russian Journal of Applied Chemistry 80, no. 12 (2007): 2093–96. http://dx.doi.org/10.1134/s1070427207120170.

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Brozena, Ann, David E. Tevault, and Katherine Irwin. "Vapor Pressure of Thiodiglycol." Journal of Chemical & Engineering Data 59, no. 2 (2014): 307–11. http://dx.doi.org/10.1021/je400978j.

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Reddy, Gunda, Michael A. Major, and Glenn J. Leach. "Toxicity Assessment of Thiodiglycol." International Journal of Toxicology 24, no. 6 (2005): 435–42. http://dx.doi.org/10.1080/10915810500368878.

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Sulfur mustard (HD) undergoes hydrolysis to form various products such as thiodiglycol (TG) in biological and environmental systems. TG is a precursor in the production of HD and it is also considered as a “Schedule 2” compound (dual-use chemicals with low to moderate commercial use and high-risk precursors). Several toxicological studies on TG were conducted to assess environmental and health effects. The oral LD50 values were >5000 mg/kg in rats. It was a mild skin and moderate ocular irritant and was not a skin sensitizer in animals. It was not mutagenic in Ames Salmonella, Escherichia c
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Morrison, Kelsey A., and Brian H. Clowers. "Non-contact detection of thiodiglycol vapors and associated degradation products using atmospheric flow tube mass spectrometry." Analyst 146, no. 10 (2021): 3263–72. http://dx.doi.org/10.1039/d0an01793k.

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Veriansyah, Bambang, Jae-Duck Kim, and Jong-Chol Lee. "Supercritical Water Oxidation of Thiodiglycol." Industrial & Engineering Chemistry Research 44, no. 24 (2005): 9014–19. http://dx.doi.org/10.1021/ie050482t.

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Lee, K. Patrick, and Herbert E. Allen. "Environmental transformation mechanisms of thiodiglycol." Environmental Toxicology and Chemistry 17, no. 9 (1998): 1720–26. http://dx.doi.org/10.1002/etc.5620170911.

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Houpt, John T., Lee C. B. Crouse, Richard A. Angerhofer, Glenn J. Leach, and Gunda Reddy. "Developmental Toxicity of Thiodiglycol in Sprague-Dawley Rats." International Journal of Toxicology 26, no. 4 (2007): 365–71. http://dx.doi.org/10.1080/10915810701461993.

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Thiodiglycol (TG), a hydrolysis product of sulfur mustard (HD), is a potential contaminant of soil and water at certain military sites. To establish developmental toxicity criteria for TG, an oral developmental toxicity study was conducted in Sprague-Dawley rats. Neat thiodiglycol (99.9 %) was administered orally to mated female rats from gestation days (GDs) 5 through 19. The day of positive mating was considered day 0. A pilot study was conducted with TG at dose levels 250, 500, 1000, 2000, or 5000 mg/kg to select suitable doses for the main study. In the main study, three groups of rats (25
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Popiel, Stanisław, Jakub Nawała, Daniel Dziedzic, Martin Söderström, and Paula Vanninen. "Determination of Mustard Gas Hydrolysis Products Thiodiglycol and Thiodiglycol Sulfoxide by Gas Chromatography-Tandem Mass Spectrometry after Trifluoroacetylation." Analytical Chemistry 86, no. 12 (2014): 5865–72. http://dx.doi.org/10.1021/ac500656g.

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Adão, Maria Helena, Benilde Saramago, and Anabela C. Fernandes. "Estimation of the Surface Tension Components of Thiodiglycol." Langmuir 14, no. 15 (1998): 4198–203. http://dx.doi.org/10.1021/la970878c.

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Singh, Beer, G. K. Prasad, M. V. S. Suryanarayana, and S. Banerjee. "The reaction of thiodiglycol on metal-impregnated carbon." Carbon 39, no. 14 (2001): 2131–42. http://dx.doi.org/10.1016/s0008-6223(01)00031-8.

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Dissertations / Theses on the topic "Thiodiglycol"

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Petetin, Lilian. "Détection d'un composé organosoufre, le thiodiglycol, par des capteurs de gaz à base de dioxyde d'étain." Besançon, 2001. http://www.theses.fr/2001BESA2015.

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Les résultats présentés dans ce mémoire concernent l'étude des mécanismes d'interaction d'un composé organosoufré, le thiodiglycol (TDG), avec la surface d'un capteur de gaz à base de dioxyde d'étain. Une caractéristique de ces dispositifs est leur température de fonctionnement comprise entre 25°C et 600°C. La réponse électrique du capteur est due à la nature mais également à la concentration de l'espèce détectée. C'est la raison pour laquelle l'étude a porté dans un premier temps sur la dégradation thermique des vapeurs de TDG, afin de quantifier les composés légers susceptibles d'être formés
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Hsu, Wen-Fang, and 徐紋芳. "Analysis of Chitooligosaccharides and Determination of Thiodiglycolic Acid and Glycolic Acid in Urine by Capillary electrophoresis with Indirect UV Detection." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/18409498528890363192.

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碩士<br>國立交通大學<br>應用化學系<br>89<br>In this study, analytes that do not absorb in the UV/Vis region can be detected by capillary electrophoresis with indirect UV. The light-absorbing co-ion provides a background signal. The background signal decreases as the analyte’s zone passing through the detector. The separation of analytes by capillary electrophoresis with indirect UV offers several advantages such as high separation performance, good reproducibility, easily manipulation, minute sample consumption, and avoiding complicated derivatization process. Six chitooligosaccharides (DP=1~
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Chen, Jun-Lin, and 陳俊霖. "Association between Urinary Thiodiglycolic Acid and Non-invasive Liver Index in Residents of Dacheng Township north of No.6 naphtha cracking Complex." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/7xe7ak.

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碩士<br>國立臺灣大學<br>職業醫學與工業衛生研究所<br>106<br>Background No.6 Naphtha Cracking Complex, one of the industrial processes, produces vinyl chloride monomer (VCM) and polyvinyl chloride (PVC) by Ethylene dichloride (EDC), which might release trace level of VCM and EDC in the atmosphere. International Agency for Research on Cancer (IARC) classified VCM, EDC as group 1, 2B respectively. Both VCM and EDC can also cause liver damage and lead to liver fibrosis even cirrhosis. Upon exposure, these will be metabolized by the cytochrome P450 enzymes and be excreted through urine as thiodiglycolic acid (TdGA). A
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Books on the topic "Thiodiglycol"

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Reid, Michael T. J. Derivatisation reactions of sulphur mustard thiodiglycol and thiodiglycol sulphoxide. University of Portsmouth, School of Pharmacy and Biomedical Sciences, 2004.

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Verification of dual-use chemicals under the Chemical Weapons Convention: The case of thiodiglycol. Oxford University Press, 1991.

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Lundin, S. J. Verification of Dual-use Chemicals under the Chemical Weapons Convention: The Case of Thiodiglycol (S I P R I Chemical and Biological Warfare Studies). A SIPRI Publication, 1992.

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Book chapters on the topic "Thiodiglycol"

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Bährle-Rapp, Marina. "Thiodiglycol." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10505.

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Lee, Tsu-Shun, William A. Weigand, and William E. Bentley. "Observations of Metabolite Formation and Variable Yield in Thiodiglycol Biodegradation Process." In Biotechnology for Fuels and Chemicals. Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-2312-2_66.

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Pham, Minh-Quan K., Steven P. Harvey, William A. Weigand, and William E. Bentley. "Reactor Comparisons for the Biodegradation of Thiodiglycol, a Product of Mustard Gas Hydrolysis." In Seventeenth Symposium on Biotechnology for Fuels and Chemicals. Humana Press, 1996. http://dx.doi.org/10.1007/978-1-4612-0223-3_72.

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Bährle-Rapp, Marina. "Thiodiglycolic Acid." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10507.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with thiodiglycolic acid and phenanthroline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_35.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand dinickel(II) complex with thiodiglycolic acid and ethylenediamine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_81.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with thiodiglycolic acid and 1,8-diaminonaphthalene." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_36.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with thiodiglycolic acid and 2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_24.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with thiodiglycolic acid and 2-(aminomethyl)-pyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_38.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with thiodiglycolic acid and 5-nitro-1,10-phenanthroline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_37.

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Conference papers on the topic "Thiodiglycol"

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Hunter, Boyd V., Jason M. Cox, Michael A. Miller, Paul Harrison, and William P. Walters. "Differential excitation spectroscopy for detection of chemical threats: DMMP and thiodiglycol." In SPIE Defense + Security, edited by Augustus W. Fountain. SPIE, 2015. http://dx.doi.org/10.1117/12.2177749.

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Reports on the topic "Thiodiglycol"

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Owens, J., and C. Koester. Analysis of Thiodiglycol: Validation of Semi-Volatile Analysis by HPLC-MS/MS by EPA Method MS777. Office of Scientific and Technical Information (OSTI), 2008. http://dx.doi.org/10.2172/945866.

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