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Journal articles on the topic 'Tert-butylphenol'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Shakira, Raied M., Muhammad Kumayl Abd Wahab, Nurdiana Nordin, and Azhar Ariffin. "Antioxidant properties of butylated phenol with oxadiazole and hydrazone moiety at ortho position supported by DFT study." RSC Advances 12, no. 27 (2022): 17085–95. http://dx.doi.org/10.1039/d2ra02140d.

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12

Shpakovsky, D. B., C. N. Banti, E. M. Mukhatova, et al. "Synthesis, antiradical activity and in vitro cytotoxicity of novel organotin complexes based on 2,6-di-tert-butyl-4-mercaptophenol." Dalton Trans. 43, no. 18 (2014): 6880–90. http://dx.doi.org/10.1039/c3dt53469c.

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13

Lao, Zhixiong, Mingmin Zhong, Yin Liang, et al. "SERS Substrate Based on Ag Nanoparticles@Layered Double Hydroxide@graphene Oxide and Au@Ag Core–Shell Nanoparticles for Detection of Two Taste and Odor Compounds." Chemosensors 12, no. 7 (2024): 137. http://dx.doi.org/10.3390/chemosensors12070137.

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Sulfide organics and phenols are ubiquitous in freshwater lakes all over the world. As two taste and odor (T and O) compounds, they are harmful to the environment and human body. The existing detection methods for T and O compounds mainly include sensory analysis and gas-phase mass spectrometry, which are cumbersome and time-consuming. Herein, a method for the simultaneous and rapid detection of two T and O compounds (methyl sulfide and 2,4-di-tert-butylphenol) based on surface-enhanced Raman spectroscopy (SERS) is firstly developed. The SERS substrate was prepared by coating Ag nanoparticles

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14

Belostotskaya, I. S., N. L. Komissarova, O. V. Shubina, E. A. Grishina, and V. V. Ershov. "Hydroxymethylation of 2,4-di-tert-butylphenol." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 39, no. 9 (1990): 1980–81. http://dx.doi.org/10.1007/bf00958283.

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15

Toyama, T., Y. Kainuma, S. Kikuchi, and K. Mori. "Biodegradation of bisphenol A and 4-alkylphenols by Novosphingobium sp. strain TYA-1 and its potential for treatment of polluted water." Water Science and Technology 66, no. 10 (2012): 2202–8. http://dx.doi.org/10.2166/wst.2012.453.

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We investigated the use of Novosphingobium sp. strain TYA-1 for the simultaneous removal of bisphenol A (BPA) and 4-alkylphenols (4-APs) from complex polluted waters. Strain TYA-1 degraded BPA and utilized it as a sole carbon and energy source via oxidative skeletal rearrangement involving the cytochrome p450 monooxygenase system. Strain TYA-1 also degraded 4-APs with branched side alkyl chains (4-tert-butylphenol [4-tert-BP], 4-sec-butylphenol, 4-tert-pentylphenol, 4-tert-octylphenol [4-tert-OP], and branched nonylphenol mixture) via 4-alkylcatechols but could not degrade 4-APs with linear si

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16

Graziano, Brendan J., Bradley M. Wile та Matthias Zeller. "Palladium(II) complexes of a bridging amine bis(phenolate) ligand featuring κ2 and κ3 coordination modes". Acta Crystallographica Section E Crystallographic Communications 75, № 8 (2019): 1265–69. http://dx.doi.org/10.1107/s2056989019010454.

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Bidentate and tridentate coordination of a 2,4-di-tert-butyl-substituted bridging amine bis(phenolate) ligand to a palladium(II) center are observed within the same crystal structure, namely dichlorido({6,6′-[(ethane-1,2-diylbis(methylazanediyl)]bis(methylene)}bis(2,4-di-tert-butylphenol))palladium(II) chlorido(2,4-di-tert-butyl-6-{[(2-{[(3,5-di-tert-butyl-2-hydroxyphenyl)methyl](methyl)amino}ethyl)(methyl)amino]methyl}phenolato)palladium(II) methanol 1.685-solvate 0.315-hydrate, [PdCl2(C34H56N2O2)][PdCl(C34H55N2O2)]·1.685CH3OH·0.315H2O. Both complexes exhibit a square-planar geometry, with un

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17

Zaikov, Gennady, and Alexander Volod’kin. "Alkylation of 2,6-di-tert-Butylphenol with Methyl Acrylate Catalyzed by Potassium 2,6-di-tert-Butylphenoxide." Chemistry and Chemical Technology 4, no. 2 (2010): 101–5. http://dx.doi.org/10.23939/chcht04.02.101.

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The kinetics of catalytic alkylation of 2,6-di-tert-butylphenol (ArOH) with methyl acrylate (MA) in the presence of potassium 2,6-di-tert-butylphenoxide (ArOK) depends on the method for the preparation of ArOK. The reaction of ArOH with KOH at temperatures > 453 K affords monomeric ArOK, which properties differ from those in the case of potassium 2,6-di-tert-butylphenoxide synthesized by the earlier methods. The regularities of ArOH alkylation depend on the ArOK concentration, the ArOH:MA ratio, and the effect of microadditives of polar solvents.

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18

Nizheharodava, Darya B., Galina A. Ksendzova, Aliaksei G. Sysa, et al. "Effects of 2-amino-4,6-di-tert-butylphenol derivatives on the viability and functional state of human peripheral blood lymphocytes." Journal of the Belarusian State University. Biology, no. 3 (December 31, 2020): 19–28. http://dx.doi.org/10.33581/2521-1722-2020-3-19-28.

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Derivatives of 2-amino-4,6-di-tert-butylphenol exhibit antiviral properties and radical regulatory activity against various types of organic radicals which determines the actuality of their further investigation. But the question of aminophenol derivatives immunomodulatory activity remains open. In this regard, the aim of the study was to assess the effects of 2-amino-4,6-di-tert-butylphenol derivatives on the viability and functional potential of human peripheral blood lymphocytes. As a result of the studies, it was shown that aminophenol compounds at concentrations of 10–5–10–7 mol did not e

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19

Kumar, K. Dinesh, J. Vigneshwari J. Vigneshwari, A. Gnanasekaran A. Gnanasekaran, V. Selvamani V. Selvamani, and P. K. Senthilkumar. "Multipotential Secondary Metabolites from Nocardiopsis dassonovillei of Marine Actinomycetes and their In Silico studies." Biosciences Biotechnology Research Asia 20, no. 1 (2023): 173–87. http://dx.doi.org/10.13005/bbra/3079.

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ABSTRACT: Actinomycetes are one of the important secondary metabolite producers. Researchers focused on the exclusive marine areas for isolation and identification of marine actinomycetes. The present study focused on the isolation and identification of Nocardiopsis dassonovillei (ON627850) from TS Pettai region. The potential strainTSP1 showed effective antibacterial activity against Haemophilus influenza. TSP1 isolates showed IC50 value of 75.22 μg/ml effective antioxidant activity determined by DPPH assay. Cytotoxicity assay results were noted for the ethyl acetate extract of TSP1 screened

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20

Nesměrák, Karel, Ivan Němec, Martin Štícha, Jiří Gabriel, and Valentin Mirceski. "Electrochemical Oxidation of Probucol in Anhydrous Acetonitrile." Collection of Czechoslovak Chemical Communications 64, no. 7 (1999): 1100–1110. http://dx.doi.org/10.1135/cccc19991100.

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Electrochemical oxidation of probucol in anhydrous acetonitrile was studied as a model of the metabolic oxidation of the substance. The study was performed by DC voltammetry, potentiostatic coulometry, cyclic voltammetry and preparative electrolysis. Probucol gives a single anodic wave E1/2 = 0.92 V. Cyclic voltammetry showes that its electrooxidation proceeds by formation of probucol radical. 2,6-Di-tert-butyl-4-(isopropylsulfanyl)phenol, 2,6-di-tert-butyl-4-sulfanylphenol, 2,6-di-tert-butyl-4-methylphenol and 2,6-di-tert-butylphenol were isolated as products of electrochemical oxidation.

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21

Medić, Ana, Ksenija Stojanović, Lidija Izrael-Živković, et al. "A comprehensive study of conditions of the biodegradation of a plastic additive 2,6-di-tert-butylphenol and proteomic changes in the degrader Pseudomonas aeruginosa san ai." RSC Advances 9, no. 41 (2019): 23696–710. http://dx.doi.org/10.1039/c9ra04298a.

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22

Li, Xinxin, Xiuhong Wang, Xiangyuan Shi, et al. "Antifungal Effect of Volatile Organic Compounds from Bacillus velezensis CT32 against Verticillium dahliae and Fusarium oxysporum." Processes 8, no. 12 (2020): 1674. http://dx.doi.org/10.3390/pr8121674.

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The present study focuses on the inhibitory effect of volatile metabolites released by Bacillus velezensis CT32 on Verticillium dahliae and Fusarium oxysporum, the causal agents of strawberry vascular wilt. The CT32 strain was isolated from maize straw compost tea and identified as B. velezensis based on 16S rRNA gene sequence analysis. Bioassays conducted in sealed plates revealed that the volatile organic compounds (VOCs) produced by the strain CT32 possessed broad-spectrum antifungal activity against eight phytopathogenic fungi. The volatile profile of strain CT32 was obtained by headspace

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23

Behrle, Andrew C., Jessica R. Levin, Jee Eon Kim, et al. "Stabilization of MIV = Ti, Zr, Hf, Ce, and Th using a selenium bis(phenolate) ligand." Dalton Transactions 44, no. 6 (2015): 2693–702. http://dx.doi.org/10.1039/c4dt01798f.

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24

Shakun, V. A., T. N. Nesterova, and P. V. Naumkin. "Thermal Stability Study of 4-tert-Butylphenol." Petroleum Chemistry 59, no. 1 (2019): 120–27. http://dx.doi.org/10.1134/s0965544119010134.

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25

Takao, Yuko, Toshinobu Ohno, Kazuyuki Moriwaki, Fukashi Matsumoto та Jun-ichiro Setsune. "Photooxidation of phenol derivatives using μ-(dihydroxo)dipalladium(II) bisporphyrin complex". Journal of Porphyrins and Phthalocyanines 14, № 01 (2010): 64–68. http://dx.doi.org/10.1142/s108842461000174x.

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μ-(dihydroxo)dipalladium(II) complex with N21, N22-etheno bridged tetraphenylporphyrin ligand was employed in the catalytic photooxidation of phenol derivative in aerated homogeneous solution with visible light irradiation. The Pd complex promoted the degradation of p-tert-butylphenol as well as Cu phthalocyanine under basic conditions and it worked as a photosensitizer even in neutral conditions in contrast with Cu phthalocyanine. Some phenol derivatives afforded corresponding quinones selectively in this photooxidation. The present Pd complex coordinated by the bidentate porphyrin ligand sho

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26

Rokhsana, Mohammed Ismail, Qasem Almaqtri Wael, and Hassan Mohammed. "Kaolin and bentonite catalysts efficiencies for the debutylation of 2-tert-butylphenol." Chemistry International 7, no. 1 (2021): 21–29. https://doi.org/10.5281/zenodo.4018036.

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Yemeni clays (bentonite and kaolin) were used as catalysts and catalysts supported metals ions Ce, Pt, Pt-Ce, Pd, Pd-Ce, for the debutylation reaction of 2-tert-butylphenol. The two clays were characterized using atomic absorption spectroscopy, particle size analyzer and N<sub>2</sub>-BET adsorption method. The activity of debutylation reaction was found to depend on the type of the catalyst.  Kaolin based catalysts were more active than those bentonite based. The Selectivity of the catalysts was found to depend on the type of treatment that each catalyst was subjected to. The catalysts t

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27

Zahara, Kulsoom, Yamin Bibi, Saadia Masood, et al. "Isolation and Identification of Bioactive Compounds from Bidens spp. Using HPLC-DAD and GC-MS Analysis and Their Biological Activity as Anticancer Molecules." Molecules 27, no. 6 (2022): 1927. http://dx.doi.org/10.3390/molecules27061927.

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The genus Bidens a member of family Compositae, is widely documented as an ethno-medicinally important genus of plants. In the present study, anticancer potential of three ethno-medicinally important species i.e., B. bipinnata, B. biternata and B. pilosa were tested. For in-vitro evaluation, an MTT (Thiazolyl blue tetrazolium bromide) assay was performed against cervical cancer cells (HeLa), hepatocellular carcinoma (HepG), and adenocarcinoma human alveolar basal epithelial cells (A549). For in vivo evaluation, Artemia salina, Danio rerio, and Caenorhabditis elegans were used. Among all the te

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28

Hassanein, Mahmoud T., Shady S. Gerges, Mohamed A. Abdo, and Sahar H. El-Khalafy. "Studies on the oxidation of 2,6-di-tert-butylphenol by molecular oxygen catalyzed by cobalt(II) tetraarylporphyrins bound to cationic latex." Journal of Porphyrins and Phthalocyanines 09, no. 09 (2005): 621–25. http://dx.doi.org/10.1142/s1088424605000721.

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A cationic latex has been prepared by emulsion copolymerization of styrene and divinylbenzene with 2 mol.% of quaternary ammonium ion surfactant monomer. The catalytic activity of cobalt(II) sulfonated tetraarylporphrins 1-5 supported on the cationic latex 6 was investigated in the autoxidation of 2,6-di-tert-butylphenol in water. All colloidal catalysts showed good catalytic activity in the autoxidation of 2,6-di-tert-butylphenol. Reaction products were identified as 2,6-di-tert-butyl-1,4-benzoquinone and the oxidative coupling product as 3,3',5,5'-tetra-tert-butyl-4,4'-diphenoquinone. The ra

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29

Nassiri, Mahmoud. "Synthesis of 4- or 6-(3-Benzyl-2,3-Dihydrobenzo[d]Thiazol-2-yl)Phenol Derivatives by a Novel Three-Component Reaction." Journal of Chemical Research 41, no. 12 (2017): 715–17. http://dx.doi.org/10.3184/174751917x15105690662890.

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A series of 4- or 6-(3-benzyl-2,3-dihydrobenzo[ d]thiazol-2-yl)phenol derivatives was synthesised by reaction of benzothiazole or 2,6-dimethylbenzothiazole with benzyl bromide in the presence of 2,6-dimethylphenol, 2,6-di- tert-butylphenol or 2- tert-butyl-4-methylphenol. The reactions proceeded in the presence of Et3N as a base and acetonitrile as solvent under reflux for 5 h in good yields.

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30

Li, Xiang, Zhi-Gang Wang, Hou-He Chen, and Sheng-Gao Liu. "The antioxidant methyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate." Acta Crystallographica Section C Structural Chemistry 70, no. 11 (2014): 1050–53. http://dx.doi.org/10.1107/s2053229614021445.

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The title compound, C18H28O3, was prepared by the reaction of 2,6-di-tert-butylphenol with methyl acrylate under basic conditions using dimethyl sulfoxide as the promoter. The structure of this antioxidant indicates significant strain between theortho tert-butyl substituents and the phenolic OH group. In spite of the steric crowding of the OH group, it participates in intermolecular hydrogen bonding with the ester carbonyl O atom.

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Santana-Mayor, Álvaro, Giovanni D’Orazio, Miguel Ángel Rodríguez-Delgado, and Bárbara Socas-Rodríguez. "Natural Eutectic Solvent-Based Temperature-Controlled Liquid–Liquid Microextraction and Nano-Liquid Chromatography for the Analysis of Herbal Aqueous Samples." Foods 14, no. 1 (2024): 28. https://doi.org/10.3390/foods14010028.

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In this work, two novel (-)-menthol-based hydrophobic natural eutectic solvents with vanillin and cinnamic acid were prepared and applied as extraction solvents. In this regard, 12 endocrine disruptors, including phenol, 2,4-dimethylphenol, 2,3,6-trimethylphenol, 4-tert-butylphenol, 4-sec-butylphenol, 4-tert-amylphenol, 4-n-hexylphenol, 4-tert-octylphenol, 4-n-heptylphenol, 4-n-octylphenol, and 4-n-nonylphenol and bisphenol A, were studied in a green tea drink. A temperature-controlled liquid–liquid microextraction was used as the extraction method, and nano-liquid chromatography–ultraviolet d

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32

Hirata-Koizumi, Mutsuko, Masao Hamamura, Hiromi Furukawa, et al. "Elevated susceptibility of newborn as compared with young rats to 2-tert-butylphenol and 2,4-di-tert-butylphenol toxicity." Congenital Anomalies 45, no. 4 (2005): 146–53. http://dx.doi.org/10.1111/j.1741-4520.2005.00084.x.

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33

Lin, Tsung-Han, Chia-Han Chen, Chi-Shuang Chang, Ming-Chang Liu, Shing-Jong Huang, and Soofin Cheng. "Cubic Pm3n mesoporous aluminosilicates assembled from zeolite seeds as strong acidic catalysts." Catalysis Science & Technology 5, no. 6 (2015): 3182–93. http://dx.doi.org/10.1039/c5cy00184f.

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Cubic Pm3n mesoporous aluminosilicates with 3D interconnected pore structures, assembled from Al-incorporating ZSM-5 seeds at pH 9 using CTEABr as a pore-directing agent, are efficient catalysts for the alkylation of 2,4-di-tert-butylphenol with cinnamyl alcohol to form flavan.

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34

Lutz, Martin, and Anthony L. Spek. "2,6-Di-tert-butylphenol revisited at 110 K." Acta Crystallographica Section C Crystal Structure Communications 61, no. 11 (2005): o639—o641. http://dx.doi.org/10.1107/s0108270105030325.

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Církva, Vladimír, Jana Kurfürstová, Jindřich Karban, and Milan Hájek. "Microwave photochemistry III: Photochemistry of 4-tert-butylphenol." Journal of Photochemistry and Photobiology A: Chemistry 174, no. 1 (2005): 38–44. http://dx.doi.org/10.1016/j.jphotochem.2005.03.004.

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Komissarova, N. L., I. S. Belostotskaya, O. V. Shubina, V. V. Ershov, V. N. Voznesenskii, and I. I. Chervin. "Anomalous Duff reaction with 2,4-di-tert-butylphenol." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 9 (1988): 1966. http://dx.doi.org/10.1007/bf00962532.

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Silberova, B., and L. Cerveny. "Hydrogenation of 2-tert-butylphenol over Ni catalyst." Reaction Kinetics and Catalysis Letters 67, no. 1 (1999): 29–33. http://dx.doi.org/10.1007/bf02475823.

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BELOSTOTSKAYA, I. S., N. L. KOMISSAROVA, O. V. SHUBINA, E. A. GRISHINA, and V. V. ERSHOV. "ChemInform Abstract: Hydroxymethylation of 2,4-Di-tert-butylphenol." ChemInform 22, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199136166.

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Konuspaev, Sapar R., Khairulla N. Zhanbekov, Natalya V. Kul'Kova, and Dmitry Yu Murzin. "Kinetics of 4-tert-butylphenol hydrogenation over rhodium." Chemical Engineering & Technology 20, no. 2 (1997): 144–48. http://dx.doi.org/10.1002/ceat.270200212.

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Hasegawa, Ryuichi, Mutsuko Hirata-Koizumi, Masao Hamamura, et al. "Higher susceptibility of newborn rats to 2-tert-butylphenol and 2,4-di-tert-butylphenol toxicity as compared with young rats." Toxicology Letters 172 (October 2007): S210—S211. http://dx.doi.org/10.1016/j.toxlet.2007.05.530.

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Zimerson, Erik, Magnus Bruze, and An Goossens. "Simultaneous p-tert-Butylphenol-Formaldehyde Resin and p-tert-Butylcatechol Contact Allergies in Man and Sensitizing Capacities of p-tert-Butylphenol and p-tert-Butylcatechol in Guinea Pigs." Journal of Occupational & Environmental Medicine 41, no. 1 (1999): 23–28. http://dx.doi.org/10.1097/00043764-199901000-00005.

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42

Mergenbayeva, Saule, Alisher Kumarov, Timur Sh Atabaev, et al. "Degradation of 4-Tert-Butylphenol in Water Using Mono-Doped (M1: Mo, W) and Co-Doped (M2-M1: Cu, Co, Zn) Titania Catalysts." Nanomaterials 12, no. 14 (2022): 2326. http://dx.doi.org/10.3390/nano12142326.

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Mono-doped (Mo-TiO2 and W-TiO2) and co-doped TiO2 (Co-Mo-TiO2, Co-W-TiO2, Cu-Mo-TiO2, Cu-W-TiO2, Zn-Mo-TiO2, and Zn-W-TiO2) catalysts were synthesized by simple impregnation methods and tested for the photocatalytic degradation of 4-tert-butylphenol in water under UV (365 nm) light irradiation. The catalysts were characterized with various analytical methods. X-ray diffraction (XRD), Raman, Diffuse reflectance (DR) spectroscopies, Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and Energy dispersive spectroscopy (EDS) were applied to investigate the structure, optic

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43

Li, Xia, Hai-Jing Hu, Jing-Yu Li, Cong Wang, Shuang-Lin Chen, and Shu-Zhen Yan. "Effects of the Endophytic Bacteria Bacillus cereus BCM2 on Tomato Root Exudates and Meloidogyne incognita Infection." Plant Disease 103, no. 7 (2019): 1551–58. http://dx.doi.org/10.1094/pdis-11-18-2016-re.

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Root-knot nematodes (Meloidogyne spp.) cause serious crop losses worldwide. The colonization of tomato roots by endophytic bacteria Bacillus cereus BCM2 can greatly reduce Meloidogyne incognita damage, and tomato roots carrying BCM2 were repellent to M. incognita second-stage juveniles (J2). Here, the effects of BCM2 colonization on the composition of tomato root exudates was evaluated and potential mechanisms for BCM2-mediated M. incognita control explored using a linked twin-pot assay and GC-MS. On water agar plates, J2 preferentially avoided filter paper treated with tomato root exudates (o

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44

Sponza, Deli̇a Teresa, and Ruki̇ye Özteki̇n. "Zeolitic Imidazolate/Fe3O4 Nanocomposite for Removal of Polystyrene and 4-tert-butylphenol via Adsorption." WSEAS TRANSACTIONS ON ENVIRONMENT AND DEVELOPMENT 19 (October 17, 2023): 1071–82. http://dx.doi.org/10.37394/232015.2023.19.101.

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Simultaneous removal of microplastics and endocrine disruptors was performed with high yields using Zeolitic imidazolate/Fe3O4 nanocomposite. Polystyrene and 4-tert-butylphenol were used to indicate the microplastic and endocrine disruptors. Under optimal conditions for maximum yields, the matrix was as follows: 1.5 mg/l Zeolitic imidazolate/Fe3O4 nanocomposite, 30 min adsorption time at a Zeolitic imidazolate to Fe3O4 ratio of 1/1, and 6 mg/l individual polystyrene 4-tert-butylphenol concentrations. Under these conditions, 99% and 98% removals were detected for polystyrene and 4-tert-butylphe

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Kut, Oemer M., Urs R. Daetwyler, and Guenther Gut. "Stereoselective hydrogenation of 2-tert-butylphenol to cis-2-tert-butylcyclohexanol. 1. Equilibrium composition of the system 2-tert-butylphenol/2-tert-butylcyclohexanone/cis- or trans-2-tert-butylcyclohexanol and hydrogen." Industrial & Engineering Chemistry Research 27, no. 2 (1988): 215–18. http://dx.doi.org/10.1021/ie00074a001.

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Volod´kin, Alexander, and Gennady Zaikov. "Mechanism of Catalytic Alkylation of 2,6-di-tert-Butylphenol by Methyl Acrylate." Chemistry & Chemical Technology 6, no. 1 (2012): 31–34. http://dx.doi.org/10.23939/chcht06.01.031.

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Kamalakar, Gunda, Kenichi Komura, and Yoshihiro Sugi. "tert-Butylation of Phenol over Ordered Solid Acid Catalysts in Supercritical Carbon Dioxide: Efficient Synthesis of 2,4-Di-tert-butylphenol and 2,4,6-Tri-tert-butylphenol." Industrial & Engineering Chemistry Research 45, no. 18 (2006): 6118–26. http://dx.doi.org/10.1021/ie060440k.

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48

Sang, Mee Kyung, Jeong Do Kim, Beom Seok Kim, and Ki Deok Kim. "Root Treatment with Rhizobacteria Antagonistic to Phytophthora Blight Affects Anthracnose Occurrence, Ripening, and Yield of Pepper Fruit in the Plastic House and Field." Phytopathology® 101, no. 6 (2011): 666–78. http://dx.doi.org/10.1094/phyto-08-10-0224.

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We previously selected rhizobacterial strains CCR04, CCR80, GSE09, ISE13, and ISE14, which were antagonistic to Phytophthora blight of pepper. In this study, we investigated the effects of root treatment of rhizobacteria on anthracnose occurrence, ripening, and yield of pepper fruit in the plastic house and field in 2008 and 2009. We also examined the effects of volatiles produced by the strains on fruit ripening and on mycelial growth and spore development of Colletotrichum acutatum and Phytophthora capsici in the laboratory, identifying the volatile compounds by gas chromatography–mass spect

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Knizek, Jörg, and Heinrich Nöth. "Unusual Formation of Two New Titanium(IV) Tetraphenolates." Zeitschrift für Naturforschung B 66, no. 1 (2011): 58–64. http://dx.doi.org/10.1515/znb-2011-0110.

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When the product of the reaction of 2,6-di-tert.-butylphenol with TiCl4 in a 3:1 ratio is treated with Na[HBEt3], the isolated product is not (2,6-tert.-Bu2C6H3O)3Ti(HBEt3) but the isomerized ester (2,4-tert.-Bu2C6H3O)4Ti with molecular S4 symmetry. This rearrangement of the R substituents does not occur upon reacting 2,6-diisopropylphenol with TiCl4 and Na[HBEt3]. An unexpected result is also observed for the product of the reaction of tris(2,6-diisopropylphenolato)titanium(IV) chloride with lithium bis(pentafluorophenolato)dihydridoborate. The isolated product proved to be dimeric tris(penta

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Adão, Pedro, João Reboleira, Marco Teles, et al. "Enhancement of the Antioxidant and Antimicrobial Activities of Porphyran through Chemical Modification with Tyrosine Derivatives." Molecules 26, no. 10 (2021): 2916. http://dx.doi.org/10.3390/molecules26102916.

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The chemical modification of porphyran hydrocolloid is attempted, with the objective of enhancing its antioxidant and antimicrobial activities. Sulfated galactan porphyran is obtained from commercial samples of the red algae Porphyra dioica using Soxhlet extraction with water at 100 °C and precipitation with isopropyl alcohol. The extracted porphyran is then treated with modified L-tyrosines in aqueous medium in the presence of NaOH, at ca. 70 °C. The modified tyrosines L1 and L2 are prepared through a Mannich reaction with either thymol or 2,4-di-tert-butylphenol, respectively. While the reac

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