Academic literature on the topic '2-Ethylhexanol'
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Journal articles on the topic "2-Ethylhexanol"
Keith, Y., M. C. Cornu, P. M. Canning, J. Foster, J. C. Lhuguenot, and C. R. Elcombe. "Peroxisome proliferation due to di (2-ethylhexyl) adipate, 2-ethylhexanol and 2-ethylhexanoic acid." Archives of Toxicology 66, no. 5 (May 1992): 321–26. http://dx.doi.org/10.1007/bf01973626.
Full textMiura, Motofumi, Masaharu Toriyama, and Shigeyasu Motohashi. "Novel Synthesis of Optically Active 2‐Ethylhexanoic Acid, 2‐Ethylhexanol, and 2‐Ethylhexylamine via the Asymmetric Favorskii Rearrangement." Synthetic Communications 36, no. 3 (January 2006): 259–64. http://dx.doi.org/10.1080/00397910500374740.
Full textRitter, E. J., W. J. Scott, J. L. Randall, and J. M. Ritter. "Teratogenicity of di(2-ethylhexyl) phthalate, 2-ethylhexanol, 2-ethylhexanoic acid, and valproic acid, and potentiation by caffeine." Teratology 35, no. 1 (February 1987): 41–46. http://dx.doi.org/10.1002/tera.1420350107.
Full textBui, Linh M., Marie W. Taubeneck, Joel F. Commisso, Janet Y. Uriu-Hare, Willem D. Faber, and Carl L. Keen. "Altered zinc metabolism contributes to the developmental toxicity of 2-ethylhexanoic acid, 2-ethylhexanol and valproic acid." Toxicology 126, no. 1 (February 1998): 9–21. http://dx.doi.org/10.1016/s0300-483x(97)00171-6.
Full textBhutada, S. R., and V. G. Pangarkar. "Esterification of phthalic anhydride with 2-ethylhexanol." Journal of Chemical Technology & Biotechnology 36, no. 2 (April 24, 2007): 61–66. http://dx.doi.org/10.1002/jctb.280360204.
Full textNalli, Sandro, Owen J. Horn, Adam R. Grochowalski, David G. Cooper, and Jim A. Nicell. "Origin of 2-ethylhexanol as a VOC." Environmental Pollution 140, no. 1 (March 2006): 181–85. http://dx.doi.org/10.1016/j.envpol.2005.06.018.
Full textLiang, Ning, Xiaolong Zhang, Hualiang An, Xinqiang Zhao, and Yanji Wang. "Direct synthesis of 2-ethylhexanol via n-butanal aldol condensation–hydrogenation reaction integration over a Ni/Ce-Al2O3 bifunctional catalyst." Green Chemistry 17, no. 5 (2015): 2959–72. http://dx.doi.org/10.1039/c5gc00223k.
Full textDarracq, G., A. Couvert, C. Couriol, A. Amrane, and P. Le Cloirec. "Absorption and biodegradation of hydrophobic volatile organic compounds: determination of Henry's constants and biodegradation levels." Water Science and Technology 59, no. 7 (April 1, 2009): 1315–22. http://dx.doi.org/10.2166/wst.2009.124.
Full textKeith, Y., P. M. Canning, J. C. Lhuguenot, and C. R. Elcombe. "Peroxisome Proliferation due to di-(2-Ethylhexyl)adipate and 2-Ethylhexanol." Human Toxicology 4, no. 5 (September 1985): 551–52. http://dx.doi.org/10.1177/096032718500400540.
Full textKELLER, B., D. LIANG, and R. THURMAN. "2-Ethylhexanol uncouples oxidative phosphorylation in rat liver mitochondria." Toxicology Letters 57, no. 1 (June 1991): 113–20. http://dx.doi.org/10.1016/0378-4274(91)90125-p.
Full textDissertations / Theses on the topic "2-Ethylhexanol"
Ellis, Shawn Alfred. "2-ethylhexanol, a potential biological indicator of occupational exposure to the plasticizer di(2-ethylhexyl)phthalate." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq28742.pdf.
Full textDewidar, Assem A. "Impact of Biosurfactants on Biodegradation of a Binary Mixture of Hydrophilic and Hydrophobic VOCs in Trickle Bed Air Biofilter." University of Cincinnati / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1563272543717587.
Full textDutescu, Ralf Michael [Verfasser], and H. G. [Akademischer Betreuer] Wahl. "Expressionsanalyse der nukleären Rezeptoren PPAR-α/γ-1/γ-2 [PPAR-alpha, gamma-1, gamma-2] und der Transkriptionsfaktoren T-bet und GATA-3 nach Stimulation von dermalen Endothelzellen mit den Weichmacher, Di(2-ethylhexyl)phthalat-Metaboliten-2-Ethylhexanol und 4-Heptanon / Ralf Michael Dutescu. Betreuer: H. G. Wahl." Marburg : Philipps-Universität Marburg, 2011. http://d-nb.info/1013288459/34.
Full textCosta, Daniela Filipa de Oliveira. "Hepatic differentiation of skin-derived stem cells and their application within in vitro toxicity testing." Master's thesis, 2016. http://hdl.handle.net/10451/34619.
Full textSteatosis is the hepatic accumulation of lipids. Despite being the least severe stage of Non-Alcoholic fatty liver disease, evaluation of steatosis is a mechanistic assay for toxin-induced liver injury, mandatory for the development of new chemical entities. Toxin-induced liver injury represent a major concern to the pharmaceutical industry. The discontinuation of the development of new compounds, in addition with the withdrawal of market drugs, represent an immense economic impact, prompting an immense pressure to develop a predictable human-based in vitro hepatic model. HepG2 and HepaRG cell lines are the most used in vitro models for hepatotoxic evaluation. Nevertheless, this cell models neglect to represent the human hepatic metabolism. Alternatively, stem-cells derived hepatic cells, specifically human skin-derived precursors differentiated into hepatic cells (hSKP-HPC), are emerging as a new potential hepatotoxic in vitro study system. So as to compare the potential of hSKP-HPC, to the other two hepatic cell lines, cells were incubated with three widely known steatogenic compounds, oleic acid, tetracycline and 2-ethylhexanol, and cell viability, lipid accumulation and gene expression analysis was performed. Preliminary results revealed significant difference in sensitivity of the three cell lines to hepatotoxins. Indeed, HepaRG revealed the lowest accumulation of neutral lipids, where hSKP-HPC was shown to be exceptionally sensitive. Moreover, different gene expression profiles between HepaRG and hSKP-HPC revealed distinct steatosis induction mechanisms. While tetracycline decreased efflux of FAs and increased de novo lipogenesis in hSKP-HPC, further contributing for steatosis phenotype, a compensatory mechanisms was found in HepaRG cells. A similar finding was made in HepaRG cells incubated with 2-ethylhexanol, where an increase uptake of FAs was perceived, while the opposite was found in hSKP-HPC cells. Despite these differences, some parallelisms in key pathogenic mechanisms were detected. Ultimately, our preliminary results demonstrated that hSKP-HPC are a possible in vitro model for hepatotoxic evaluation.
A esteatose é definida como a acumulação hepática de lípidos. Apesar de ser a condição mais benigna dentro do espectro do fígado gordo não alcoólico, a esteatose é um mecanismo de lesão hepática induzida por toxinas, de análise obrigatória no desenvolvimento de novas entidades químicas. Lesões hepáticas induzidas por toxinas são uma grande preocupação da indústria farmacêutica. A descontinuação do estudo de novos compostos, assim como a retirada de medicamentos do mercado representam um enorme impacto económico, originando uma enorme pressão para o desenvolvimento de um modelo in vitro hepático humano fiável. As linhas celulares HepG2 e HepaRG são os modelos in vitro para avaliação hepatotóxica mais comuns. No entanto, estes modelos falham em representar fielmente o metabolismo hepático humano. Em alternativa, células hepáticas derivadas de células estaminais, especificamente células hepáticas diferenciadas de precursores derivados da pele humana (hSKP-HPC), estão a surgir como um novo sistema in vitro para o estudo de hepatotóxicos. De forma a comparar a potencialidade deste sistema, as linhas celulares anteriormente referenciadas foram incubadas com três compostos esteatogénicos: ácido oleico, tetraciclina, 2-etilhexanol, e a viabilidade celular, acumulação lipídica e análise de expressão genética foi realizada. Resultados preliminares revelam uma diferença significativa na sensibilidade das três linhas celulares às hepatotoxinas. De facto, as células HepaRG revelaram pouca acumulação de lípidos neutros, enquanto hSKP-HPC demostrou ser um modelo celular particularmente sensível. Adicionalmente, diferentes padrões de expressão genética entre as culturas celulares HepaRG e hSKP-HPC sugerem a ativação de diferentes mecanismos de indução de esteatose. Enquanto a incubação com tetraciclina originou uma diminuição dos níveis de mRNA de proteínas envolvidas com o efluxo de ácidos gordos e um aumento da lipogénese nas células hSKP-HPC, que contribuem para o fenótipo de esteatose, um mecanismo de feedback negativo foi visualizado nas células HepaRG. Uma observação também encontrada aquando o tratamento com 2-etilhexanol, onde um aumento do uptake de ácidos gordos foi considerado um mecanismo de indução de esteatose, enquanto o oposto foi encontrado nas células hSKP-HPC. Apesar destas diferenças, alguns paralelismos em mecanismos chave na indução de esteatose foram detetados. Em última analise, resultados preliminares demostram que hSKP-HPC é um modelo in vitro com potencial para avaliação hepatotóxica.
YE, WUN-DE, and 葉文德. "Isobaric vapor-liquid equilibrium for binary mixtures containing of n-octanol、2-Ethyl-1-hexanol、Octanoic acid、2-Ethylhexanoic acid and 2-Ethyl-2-hexenal." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/59560869594737355402.
Full textBooks on the topic "2-Ethylhexanol"
Environment, Alberta Alberta. Assessment report on 2-ethylhexanol for developing ambient air quality objectives. [Edmonton]: Alberta Environment, 2004.
Find full text2-ethylhexanol: A potential biological indicator of occupational exposure to the plasticizer di(2-ethylhexyl)phthalate. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1999.
Find full textBook chapters on the topic "2-Ethylhexanol"
van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "2-Ethylhexanoic acid." In Spectra for the Identification of Additives in Food Packaging, 185–89. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_36.
Full textHong, Chua, Gek Sim Yap Miranda, and Jem Ng Wun. "A Mathematical Model for the Anaerobic Degradation of 2-Ethylhexanoic Acid." In Biochemical Engineering for 2001, 800–803. Tokyo: Springer Japan, 1992. http://dx.doi.org/10.1007/978-4-431-68180-9_213.
Full text"2-Ethylhexanol." In Toxicological Evaluations, 181–205. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84195-8_11.
Full text"2-Ethylhexanol." In Toxicological Evaluations, 103–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59835-7_7.
Full textGrzesik, M., and T. Gumula. "Kinetics models for esterification of levulinic acid with 2-ethylhexanol using different catalysts." In Reaction Kinetics and the Development and Operation of Catalytic Processes, Proceedings of the 3rd International Symposium, 547–51. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)82010-3.
Full text"Table IV: Volatile compounds identified in the dust of swine confinement units Hydrocarbons Ketones Hexane 1) Acetone 4) «t-Pinen 1) Butanone 4) Limonen 1) Pentanone 4) 3,7,7-Trimethyl -Octanone 4) bicyclo (3,1,1)-l-0ctene-3-one 4) 2-Hepten 1) Benzene 1) Acids Toluene 1) Acetic 4)5)6) Alcohols Propionic 4)5)6) i-Butyric 1)5)6) 1-Pentanol 1) Butyric 4)5)6) 1-Heptanol 1) 1-Valeric 5)6) 4-Methylcyclo-Valeric 4)5)6) hexanol 1) Hexanoic 4)5) 2-Ethylhexanol 1) Heptanoic 4) Octanoic 4) Phenols Nonanoic 4) Decanoic 4) Phenol 1)3)6) Undecanoic 4) p-Cresol 3)4)6) Dodecanoic 4) o-Cresol 1) Laurie 3) p-Ethylphenol 3)6) Tridecanoic 4) o-Ethylphenol 4) Tetradecanoic 4) m-Ethylphenol 4) Benzoic 4) Phenyl acetic 3)4) Indoles 3-Phenyl propionic 3) Hydrocinnamic 4) Indole 2)6) Skatole 2)3)6) Miscellaneous Compounds Aldehydes 2-Pentylfuran 3) Vanillin 3) Butanal 4) 2-Butenal 4) Pentanal 4) 2-Pentenal 4) Hexanal 1)3)4) 1) = WEURMAN (13) 2-Hexenal 4) 2) = TRAVIS and ELLIOTT (31) Heptanal 1)3) 2-Heptenal 4) 3) = HAMMOND et al. (30) 2.4-Heptadienal 3)4) 4) = HAMMOND et al. (40) Nonanal 3) 2-Nonenal 3) 5) = AENGST (33) 2.4-Nonadienal 3)4) 6) = HARTUNG (34) Decanal 4) 2.4-Decadienal 3)4) Benzaldehyde 1)4)." In Odour Prevention and Control of Organic Sludge and Livestock Farming, 344. CRC Press, 1986. http://dx.doi.org/10.1201/9781482286311-138.
Full textConference papers on the topic "2-Ethylhexanol"
Purdham, J., A. Sass-Kortsak, P. Bozek, and S. Ellis. "186. Feasibility Study on the Use of 2-Ethylhexanol as a Biological Indicator of Di-(2-Ethylhexyl)Phthalate Exposure." In AIHce 1999. AIHA, 1999. http://dx.doi.org/10.3320/1.2763023.
Full textLiu, Mingyan, Kwanghoon Baek, Fransico Argüelles Vivas, Gayan Aruna Abeykoon, and Ryosuke Okuno. "Effects of Surfactant Partitioning Coefficient and Interfacial Tension on the Oil Displacement in Low-Tension Polymer Flooding." In SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206220-ms.
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