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Relevant bibliographies by topics / Tert-butylphenol

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Academic literature on the topic 'Tert-butylphenol'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Tert-butylphenol"

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Toyama, Tadashi, Naonori Momotani, Yuka Ogata, et al. "Isolation and Characterization of 4-tert-Butylphenol-Utilizing Sphingobium fuliginis Strains from Phragmites australis Rhizosphere Sediment." Applied and Environmental Microbiology 76, no. 20 (2010): 6733–40. http://dx.doi.org/10.1128/aem.00258-10.

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ABSTRACT We isolated three Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment that were capable of utilizing 4-tert-butylphenol as a sole carbon and energy source. These strains are the first 4-tert-butylphenol-utilizing bacteria. The strain designated TIK-1 completely degraded 1.0 mM 4-tert-butylphenol in basal salts medium within 12 h, with concomitant cell growth. We identified 4-tert-butylcatechol and 3,3-dimethyl-2-butanone as internal metabolites by gas chromatography-mass spectrometry. When 3-fluorocatechol was used as an inactivator of meta-cleavage enzymes, s

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Lasocha, B., M. Grzywa, and W. Lasocha. "Powder diffraction investigations of 2,2′-Thiobis(4-methyl-6-tert-butylphenol) and 2,2′-Methylenebis(4-methyl-6-tert-butylphenol)." Powder Diffraction 20, no. 1 (2005): 67–70. http://dx.doi.org/10.1154/1.1835961.

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X-ray diffraction investigations of two phenol derivatives - 2,2′-Thiobis(4-methyl-6-tert-butylphenol) and 2,2′-Methylenebis(4-methyl-6-tert-butylphenol) were carried out. Both compounds at room temperature have similar cell volume and the same number of molecules in an unit cell. However, 2,2′-Thiobis(4-methyl-6-tert-butylphenol) crystallizes in the monoclinic system with unit cell parameters refined to a=0.8278(2) nm, b=1.2968(4) nm, c=1.9493(7) nm, β=90.93(2)°, space group P21∕n(14), whereas 2,2′-Methylenebis(4-methyl-6-tert-butylphenol) crystallizes in the orthorhombic system with unit cel

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Gizur, Tibor, György G. Ferenczy, Éva Ágai-Csongor, and György Domány. "Antioxidant Building Blocks I. The Unexpected C-Acetylation of 2,6-Di-tert-butylphenol with Isopropenyl Acetate." Collection of Czechoslovak Chemical Communications 61, no. 8 (1996): 1244–47. http://dx.doi.org/10.1135/cccc19961244.

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While the reaction of some 2-substituted and 2,6-disubstituted phenols with isopropenyl acetate resulted in the corresponding phenol acetates, in the reaction of 2,6-di-tert-butylphenol, a useful starting material of antioxidant building blocks, under the same conditions 4-acetyl-2,6-di- tert-butylphenol was the only product.

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Martic, Sanela. "(Digital Presentation) Electrocatalytic Transformations of Phenolic Compounds." ECS Meeting Abstracts MA2022-01, no. 25 (2022): 1212. http://dx.doi.org/10.1149/ma2022-01251212mtgabs.

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Electrocatalytic transformations giving rise to new C-C bond formation and new products are of value. We have recently discovered that phenolic compounds undergo selective electrochemical oxidation giving rise to reactive radicals which combine to produce product with new C-C bond formed [1]. A series of phenolic compounds, including butylated hydroxytoluene (BHT), 4-tert-butylphenol (4TBP), 2-tert-butylphenol (2TBP), 2,4,6-tri-tert-butylphenol (TTBP), 2,6,-di-tert-butylphenol (DTBP), diphenylphenol (DPP), and trichlosan were systematically evaluated by electrochemical methods.The selective el

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Shanina, E. L., G. E. Zaikov, and N. A. Mukmeneva. "Studies of the inhibition of autooxidation of polypropylene with 4,4′-bis(2,6-di-tert-butylphenol)." Canadian Journal of Chemistry 73, no. 11 (1995): 2011–14. http://dx.doi.org/10.1139/v95-248.

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The kinetics of 4,4′-bis(2,6-di-tert-butylphenol) (BP) consumption in the oxidation of polypropylene (PP) at 130 °C in air has been studied. It is shown that 3,3′,5,5′-tetra-tert-butyl-4,4′-diphenoquinone (DPQ) is the main product of conversion of the starting BP. An effect of synergism has been revealed on studying stabilization of PP with BP–DPQ mixtures. The antioxidative activity of BP was compared with that of some other stabilizers. Keywords: polypropylene oxidation, antioxidative activity, 4,4′-bis(2,6-di-tert-butylphenol), 3,3′,5,5′-tetra-tert-butyl-4,4′-diphenoquinone.

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Milaeva, E. R., S. I. Filimonova, N. N. Meleshonkova, et al. "Antioxidative Activity of Ferrocenes Bearing 2,6-Di-Tert-Butylphenol Moieties." Bioinorganic Chemistry and Applications 2010 (2010): 1–6. http://dx.doi.org/10.1155/2010/165482.

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The antioxidative activity of ferrocenes bearing either 2,6-di-tert-butylphenol or phenyl groups has been compared using DPPH (1,1-diphenyl-2-picrylhydrazyl) test and in the study of the in vitro impact on lipid peroxidation in rat brain homogenate and on some characteristics of rat liver mitochondria. The results of DPPH test at20∘C show that the activity depends strongly upon the presence of phenolic group but is improved by the influence of ferrocenyl fragment. The activity of N-(3,5-di-tert-butyl-4-hydroxyphenyl)iminomethylferrocene (1), for instance, was 88.4%, which was higher than the a

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Volod´kin, Alexander, and Gennady Zaikov. "Potassium and Sodium 2,6-Di-tert-Butyl Phenoxides and their Properties." Chemistry & Chemical Technology 4, no. 3 (2010): 179–84. http://dx.doi.org/10.23939/chcht04.03.179.

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The determining factor of the reaction of 2,6-di-tert-butylphenol with alkaline metal hydroxides is temperature, depending on which two types of potassium or sodium 2,6-di-tert-butyl phenoxides are formed with different catalytic activity in alkylation of 2,6-di-tert-butylphenol with methyl acrylate. More active forms of 2,6-But2C6H3OK or 2,6-But2C6H3ONa are synthesized at temperatures higher than 433 K representing predominantly monomers of 2,6-di-tert-butylphenoxides which produce dimers when cooling. The data of NMR 1Н, electronic, and IR spectra for the corresponding forms of 2,6-But2C6H3O

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Gong, Chen, Xiaomin Sun, and Chenxi Zhang. "The atmospheric chemical reaction of 4-tert-butylphenol initiated by OH radicals." Environmental Chemistry 10, no. 2 (2013): 111. http://dx.doi.org/10.1071/en12182.

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Environmental context 4-tert-Butylphenol, an environmental endocrine disruptor, can be taken in by humans and animals resulting in reproductive and developmental problems. We report a theoretical study on the degradation mechanism of 4-tert-butylphenol in the atmosphere, and calculate the atmospheric lifetime of this chemical. The data will help our understanding of the behaviour of 4-tert-butylphenol in the environment and thereby provide valuable information about its possible effect on human health. Abstract 4-tert-Butylphenol (TBP) is a typical environmental endocrine. In this paper, the O

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Aziz, A., P. Agamuthu, and SH Fauziah. "Removal of bisphenol A and 2,4-Di-tert-butylphenol from landfill leachate using plant- based coagulant." Waste Management & Research: The Journal for a Sustainable Circular Economy 36, no. 10 (2018): 975–84. http://dx.doi.org/10.1177/0734242x18790360.

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Landfill leachate contain persistent organic pollutants (POPs), namely, bisphenol A (BPA) and 2,4-Di-tert-butylphenol, which exceed the permissible limits. Thus, such landfill leachate must be treated before it is released into natural water courses. This article reports on investigations about the removal efficiency of POPs such as BPA and 2,4-Di-tert-butylphenol from leachate using locust bean gum (LBG) in comparison with alum. The vital experimental variables (pH, coagulant dosage and stirring speed) were optimised by applying response surface methodology equipped with the Box–Behnken desig

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Knaudt, Jutta, Stefan Förster, Ulrich Bartsch, Anton Rieker, and Ernst-G. Jäger. "Catalytic Oxidation of a Trialkyl-Substituted Phenol and Aniline with Biomimetic Schiff Base Complexes." Zeitschrift für Naturforschung B 55, no. 1 (2000): 86–93. http://dx.doi.org/10.1515/znb-2000-0114.

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The catalytic oxidation of 2,4.6-tri-tert-butylphenol and 2,4,6-tri-tert-butylaniline with molecular oxygen and tert-butylhydroperoxide was investigated using biomimetic Mn-, Fe- and Co-complexes as catalysts. The catalytic activity and product distribution were determined and compared with those observed in the reactions of the well-known Co(salen) complex

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Dissertations / Theses on the topic "Tert-butylphenol"

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Dätwyler, Urs Robert. "Stereoselektivität bei der katalytischen Hydrierung von 2-tert-Butylphenol /." [S.l.] : [s.n.], 1986. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=8131.

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Lee, Erin, and 李婉萍. "Simultaneous determination of 4-nonylphenol, 4-tert-octylphenol and 2,4-di-tert-butylphenol." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/15697406564051150790.

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碩士<br>國立陽明大學<br>環境衛生研究所<br>91<br>Environmental hormones are synthetic chemicals discharged in our environment with the specific characteristics of hormone mimic effect for organisms disturbing the endocrine system. In the past few years, the disclosed estrogenic characteristics of Alkylated phenolic compounds（AP）has attracted attention in Taiwan because it is the chemical widely used as the plastic plasticizer、anti-oxidants or surfactant. This study was to develop method that can simultaneously detect Nonylphenol（NP）、Octylphenol（OP）and Butylphenol（BP）, the products degradated from Alkylphen

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Jain, Shu-Ting, and 簡淑婷. "Simultaneous Determination of 4-nonylphenol, 4-tert-octylphenol and 2,4-di-tert-butylphenol in human urine." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/06592440163708168427.

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碩士<br>國立陽明大學<br>環境衛生研究所<br>90<br>Alkylphenols ( APs ) are compounds widely used as plastic, rubber additives and antioxidants and for surfactants. Alkylphenols are known estrogenic xenobiotics in fish, birds and mammals. Although some of the alkylphenols present in the environment are known to be released from plastic material, the main origin for this contaminant is from the microbial break-down of alkylphenols polyethoxylates ( APEOn ), a large group of nonionic surfactants. Nonylphenol ( NP ), octylphenol ( OP ) and butylphenol ( BP ) are the most common alkylphenols. Therefore, human usual

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Chou, Jing Shun, and 周敬順. "Extraction of 2-( diethylamino )-N-( 2,6-dimethylphenyl ) acetamide and 2,4-Di-tert-butylphenol in Cycnodes Jumbo Puff by using Supercritical Carbon Dioxide." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/37805117649658939908.

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碩士<br>長庚大學<br>化工與材料工程學系<br>102<br>In this research, we used the supercritical carbon dioxide extraction of Lidocaine and 2,4-Di-tert-butylphenol from Cycnodes(Cycd.)Jumbo Puff. In order to attain the best Lidocaine and 2,4-Di-tert-butylphenol yield, various factors such as different modifiers, extraction pressure and extraction temperature were studied. Moreover, the comparisons between the Lidocaine and 2,4-Di-tert-butylphenol yield of solvent extraction and supercritical fluid extraction have been made. The extracts were analyzed by GC-MS. The results show that when the operating conditions

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薛茂霖. "The reactions of 2,2'-(2-methoxybenzylidene)-bis-(4-methy1-6-tert-butylphenol) with trimethylaluminum::novel efficient catalysts for“living”and “immortal”polymerization of E-caprolactone." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/30603971557830198308.

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Book chapters on the topic "Tert-butylphenol"

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "2,2′-Methylenebis(4-ethyl-6-tert-butylphenol)." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_50.

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "2,2′-Methylenebis(4-methyl-6-tert-butylphenol)." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_51.

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Torii, Sigeru, Tsutomu Inokuchi, Anne-Lise Dhimane, Yositaka Araki, and Takao Maki. "Viable One-Pot Procedures for Electrooxidative Coupling of 2,6-Di-tert-butylphenol to 2,2′6′6-Tetra-tert-butyl-1,1′-biphenol." In Electroorganic Synthesis. Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-27.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear iron complex having (Fe4O6)6+ core with 2,6-bis(hydroxymethyl)-4-tert-butylphenol." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_482.

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"p-tert-Butylphenol." In Gesundheitsschädliche Arbeitsstoffe. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/352760345x.ch4.

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"*** 2,6-DI-TERT-BUTYLPHENOL." In Dangerous Properties of Industrial and Consumer Chemicals. CRC Press, 1994. http://dx.doi.org/10.1201/9781482293500-55.

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"4,4’-Methylene-bis(2,6-di-tert-butylphenol)." In Toxicological Evaluations. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84860-5_8.

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"p-tert-Butylphenol-Formaldehyd-Kondensations-produkte (niedermolekular)." In Gesundheitsschädliche Arbeitsstoffe. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603441.ch7.

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Conference papers on the topic "Tert-butylphenol"

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Shuvaev, Nikolay Olegovich, and Sergey Vasilyevich Popov. "SIMULATION OF THE TECHNOLOGICAL SCHEME OPERATION PRODUCTION OF 2,4-DI-TERT-BUTYLPHENOL." In Themed collection of papers from Foreign international scientific conference «Joint innovation - joint development». by HNRI «National development» in cooperation with PS of UA. May 2025. - Harbin (China). Crossref, 2025. https://doi.org/10.37539/250522.2025.62.63.009.

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The possibility of obtaining 2,4-di-tert-butylphenol as a commercial product is being considered. The study was conducted using the UniSim Design modeling system. A technological scheme of the process is proposed that ensures the production of commercial 2,4-di-tert-butylphenol from alkylate with its content of 99.8% by weight

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Verigina, Anastasiia Alexseevna, Tatiana Sergeevna Stepanova, and Pavel Iosifovich Pinko. "PREPARATION OF ALKYLTHIOMETHYLATED DERIVATIVES OF 2,4-DI-TERT-BUTYLPHENOL AND PRELIMINARY ASSESSMENT OF THEIR ANTIOXIDANT ACTIVITY." In IX Международная научно-практическая конференция "Инновационные аспекты развития науки и техники". KDU, Moscow, 2021. http://dx.doi.org/10.31453/kdu.ru.978-5-7913-1190-0-2021-6-14.

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This article discusses a method for the preparation of alkylthiomethyl derivatives of 2,4-di-tert-butylphenol through the interaction of the obtained Mannich bases with aliphatic thiols of various structures, as well as a preliminary assessment of the antioxidant activity by anodic voltammetry.

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Polovinkina, M. A., A. D. Osipova, V. P. Osipova, et al. "Antioxidant activity of tertiary amines with 2,6-di-tert-butylphenol and pyridine moieties." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069278.

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Haijuan Ma, Guangming Li, Yalei Zhang, Zhigang Zhang, and Ping Fang. "Characteristic and Metabolic pathways of 2,6-Di-tert-butylphenol degradation by Alcaligenes F-3-4." In 2011 Second International Conference on Mechanic Automation and Control Engineering (MACE). IEEE, 2011. http://dx.doi.org/10.1109/mace.2011.5987366.

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