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Relevant bibliographies by topics / Dimethylaniline

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Academic literature on the topic 'Dimethylaniline'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Dimethylaniline"

1

Liu, Bin, Bo Peng, Yan Jin, et al. "Developmental Toxicity and Cardiotoxicity of N, N-Dimethylaniline in Zebrafish Embryos." Toxics 13, no. 2 (2025): 125. https://doi.org/10.3390/toxics13020125.

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N, N-Dimethylaniline is an important chemical intermediate and an important metabolite of the pesticide Fenaminosulf. It is widely used in chemical production, but there is an extreme paucity of environmental risk assessments for N, N-dimethylaniline.: In this study, the cardiotoxicity of continuous exposure to N, N-dimethylaniline (20, 40, and 80 μg/mL) for 72 h was evaluated using zebrafish embryos.: The study found that N, N-dimethylaniline not only exhibits developmental toxicity to zebrafish embryos, leading to abnormalities such as pericardial edema, yolk sac edema, and spinal curvature,

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2

Zhu, Guang Ai, Yan Mao Dong, and Jia Xuan Li. "Preparation and Nonlinear Optical Properties of Poly(2,3-Dimethylaniline) Grafted Reduced Graphene Oxide." Materials Science Forum 852 (April 2016): 754–59. http://dx.doi.org/10.4028/www.scientific.net/msf.852.754.

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Poly (2,3-dimethylaniline) synthesized by a novel polymerization technique, is covalently grafted to reduced graphene oxide layers. Amide linkages formed between Poly (2,3-dimethylaniline) and reduced graphene oxide is confirmed with FTIR and Raman spectroscopy. Morphology was studied by scaning electron microscopy. The hybrid showed improved nonlinear optical properties compared to the graphene oxide precursor and the pristine poly (2, 3-dimethylaniline).

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3

Huang, Wei Chih, Yuen Chia Lin, and Wen Bih Tzeng. "Mass-analyzed threshold ionization spectroscopy of 2,6-dimethylaniline, 2,6-dimethylaniline-NHD, and 2,6-dimethylaniline-ND2." Chemical Physics Letters 551 (November 2012): 50–53. http://dx.doi.org/10.1016/j.cplett.2012.09.027.

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4

Biswas, M. K., M. K. Amin, P. K. Das, et al. "Single beam Z-scan for the calculation of nonlinear refractive index (n2) for poly(2,5-dimethylaniline)." Journal of Nonlinear Optical Physics & Materials 24, no. 03 (2015): 1550039. http://dx.doi.org/10.1142/s0218863515500393.

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An experimental work has been done to measure the nonlinear refractive index of poly(2,5-dimethylaniline) (PDMA). In this work, a continuous wave (cw) Ar-ion laser has been used to calculate n2 for a novel polymer; poly(2,5-dimethylaniline): synthesized from 2,5 dimethylaniline. The single beam Z-scan technique was used with laser beams of 514 and 488 nm wavelengths, taking PDMA in methanol solvent at different concentrations. The order of n2 was found to be of the order of ~ 10-14 esu.

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5

Khazalpour, Sadegh, and Davood Nematollahi. "Electrochemical and chemical synthesis of different types of sulfonamide derivatives of N,N-dimethyl-1,4-benzenediamine using 4-nitroso-N,N-dimethylaniline." Green Chemistry 17, no. 6 (2015): 3508–14. http://dx.doi.org/10.1039/c5gc00438a.

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Syntheses of disulfonamides and sulfonamides were carried out via the electrooxidation of 4-nitroso-N,N-dimethylaniline in the presence of arylsulfinic acids and direct reaction of 4-nitroso-N,N-dimethylaniline with arylsulfinic acids, respectively.

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6

Kovář, J., and J. Plocek. "Investigation of the arylnitroso reductase activity of pig liver aldehyde reductase." Biochemical Journal 235, no. 2 (1986): 537–43. http://dx.doi.org/10.1042/bj2350537.

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The reduction of p-nitroso-N-dimethylaniline, p-nitroso-N-diethylaniline, p-nitrosophenol and p-nitroso-N-phenylaniline with NADPH in the presence of aldehyde reductases 1 and 2 is described. The reactivity of these nitroso substrates is increased by hydrophobic substituents and those promoting OH- elimination from the molecule of the reduced substrate. NN-Dimethylbenzoquinonedi-iminium cation was proved to be the reaction product formed from p-nitroso-N-dimethylaniline. The kinetics of the reduction of p-nitroso-N-dimethylaniline catalysed with aldehyde reductase 1 are rather complex at pH 7,

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7

Penner, Samuel C., Maryam Kalvandi, and Jamie S. Ritch. "A structural study of 2,4-dimethylaniline derivatives." Acta Crystallographica Section E Crystallographic Communications 74, no. 9 (2018): 1276–80. http://dx.doi.org/10.1107/s2056989018011404.

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Crystallographic studies of nitrogen-containing small molecules aid in the elucidation of their structure–activity relationships and modes of aggregation. In this study, two previously synthesized molecules are crystallographically characterized for the first time. Reaction of 2,4-dimethylaniline with N-bromosuccinimide affords the ortho-brominated derivative 2-bromo-4,6-dimethylaniline (1; C8H10BrN), which sublimates in vacuo to afford crystals featuring hydrogen-bonded chains as well as Type I halogen–halogen interactions. Conversely, alkylation of two equivalents of 2,4-dimethylaniline with

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8

Hong, Bo, and Mary A. Fox. "Arene-functionalized polyisocyanides: photophysics of well-defined homopolymers and block copolymers for efficient light harvesting." Canadian Journal of Chemistry 73, no. 11 (1995): 2101. http://dx.doi.org/10.1139/v95-259.

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Steady-state and time-resolved fluorescence spectroscopy of the homopolymers and di- and triblock copolymers of 2-naphthylethylisocyanide (7), 9-anthrylethylisocyanide (10), and 2-phenanthrylethylisocyanide (11) exhibit emission from the isolated chromophores, i.e., naphthyl, anthryl, or phenanthryl, upon excitation at 284 or 354 nm. The absence of excimer emission in the fluorescence spectra of all these homopolymers is indicative of a rigid polymeric backbone. Fluorescence quenching in diblock copolymers containing a dimethylaniline donor block and a naphthalene or anthracene acceptor block

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9

Tzeng, W. B., J. L. Lin, and K. Narayanan. "Vibronic features of 2,6-dimethylaniline, 2,6-dimethylaniline–NHD, and 2,6-dimethylaniline–ND2 by resonant two-photon ionization mass spectrometry." Journal of the Chemical Society, Faraday Transactions 94, no. 19 (1998): 2913–17. http://dx.doi.org/10.1039/a804321c.

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10

Kovaleva, E. L., K. S. Arhipova, and I. M. Aldamova. "Current approaches to the control of process-related impurities in antibiotics." Regulatory Research and Medicine Evaluation 14, no. 6 (2024): 645–54. https://doi.org/10.30895/1991-2919-2024-14-6-645-654.

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INTRODUCTION. Antibiotic active substances have a distinct class of organic impurities other than related substances or organic solvents, namely, process-related impurities, such as N,N-dimethylaniline and 2-ethylhexanoic acid and its derivatives. These compounds are used as reagents in the production process, and national and international pharmacopoeias require that their residual levels should be controlled.AIM. This study aimed to justify the requirements for the control of process-related impurities in antibiotic active substances.MATERIALS AND METHODS. The study analysed general chapters

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Dissertations / Theses on the topic "Dimethylaniline"

1

Schmidt, Christian. "Isolation and growth physiology of N,N-dimethylaniline and 2,4-dimethylaniline degrading Sphingomonas species /." [S.l.] : [s.n.], 1994. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=10710.

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2

Puente, Neil. "Lidocaine and 2,6-dimethylaniline in bovine and human milk." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ58369.pdf.

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Sathiosatham, Muhunthan. "The synthesis and noncovalent electron-transfer studies of anthracene and dimethylaniline substituted nucleic acid bases and G-quartet formation in the absence of templating metal ions." Digital version:, 2000. http://wwwlib.umi.com/cr/utexas/fullcit?p9992906.

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Saleh, Nail Asad. "Dynamical solvent effect in 1-(9-anthryl)-3-(4-dimethylaniline) propane charge transfer reactions /." free to MU campus, to others for purchase, 2002. http://wwwlib.umi.com/cr/mo/fullcit?p3060138.

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5

Roberts, Kenneth M. "Mechanistic evaluation of N-dealkylation by cytochrome P450 using N,N-dimethylaniline N-oxides and kinetic isotope effects." Pullman, Wash. : Washington State University, 2009. http://www.dissertations.wsu.edu/Dissertations/Fall2009/k_roberts_113009.pdf.

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Ricardez, Esperanza Alicia Esteva. "Kinetics of the reaction between Cu(II) and pyridine-2-azo-p-dimethylaniline in aqueous and sodium dodecyl sulfate micellar solution." Scholarly Commons, 1994. https://scholarlycommons.pacific.edu/uop_etds/2743.

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Kinetic studies, as well as the thermodynamics of the formation of the Cu(II)-Pyridine-2-azo-p-dimethylaniline complex ion in aqueous solutions, and in the presence of sodium dodecyl sulfate (SDS) are reported. The kinetic determinations of the formation of complex were performed using the temperature jump technique. The rate constants in the forward (k$\rm \sb{f}$) and backward (k$\rm\sb{b}$) directions had values of (2.10 $\pm$ 0.97) $\times\ 10\sp7$ scM$\rm \sp{-1}s\sp{-1}$ and (10.0 $\pm$ 0.35) $\rm \times\ 10\sp{2}\ \sb{s}\sp{-1}$ respectively in aqueous solution at 25$\sp\circ$C. The num

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7

Khajehpour, Mazdak. "Solvent effects upon the charge-transfer reaction of the ADMA molecule in the excited state /." free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3025621.

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8

Hancock, Amber N. "A Radical Approach to Syntheses and Mechanisms." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/77139.

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The critically important nature of radical and radical ion mechanisms in biology and chemistry continues to be recognized as our understanding of these unique transient species grows. The work presented herein demonstrates the versatility of kinetic studies for understanding the elementary chemical reactions of radicals and radical ions. Chapter 2 discusses the use of direct ultrafast kinetics techniques for investigation of crucially important enzymatic systems; while Chapter 3 demonstrates the value of indirect competition kinetics techniques for development of synthetic methodologies for co

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9

Chao, Min-Chieh, and 趙敏傑. "Treatment of 2,6-Dimethylaniline by Electro-Fenton Process." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/58858890237662232136.

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碩士<br>嘉南藥理科技大學<br>環境工程與科學系碩士班<br>96<br>Electro-Fenton process is one of advanced oxidation processes. This method applies H2O2 and ferrous ions to produce hydroxyl radical for oxidizing the contaminants.In this study,I choose electro-Fenton and Fenton-like processes to treat 2,6-dimethylaniline. The objectives of this study included：(1) to identify the ability of direct electrolysis in oxidizing pollutant; (2) to compare the oxidation efficiency of the electro-Fenton and Fenton-like processes; (3) to determine the influences of initial pH,ferric ion,current and hydrogen peroxide concentration

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10

RickyPriambodo and 柯繼勇. "Treatment of 2,6-Dimethylaniline and Pyridine by Photo-electro-Fenton Process." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/10849827834572657096.

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碩士<br>國立成功大學<br>化學工程學系碩博士班<br>99<br>Hydroxyl radical is very reactive, underlying the chemistry of advanced oxidation processes (AOPs) for degrading organic compounds in water. Among various AOPs, Fenton’s reagent has been known to be an effective and simple oxidant. It is found that the Fenton reaction can be an efficiency enhanced in photo-electro-Fenton process since ferric may complex with certain target compounds or byproducts, especially those acting as ligands, produced by UVA light and current. The new design of our system came from the concept of promoting the ferric reduction rate, w

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Books on the topic "Dimethylaniline"

1

Canada, Canada Environment Canada, and Canada. Health and Welfare Canada., eds. 3,5-Dimethylaniline. Environment Canada, 1993.

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2

Gesellschaft Deutscher Chemiker. Beratergremium für Umweltrelevante Altstoffe., ed. N,N-Dimethylanilin. VCH, 1993.

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3

Abdo, K. NTP technical report on the toxicology and carcinogenesis studies of n,n-dimethylaniline (CAS no. 121-69-7) in F344/N rats and B6C3F1 mice (gavage studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1989.

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4

Kornreich, Mary. NTP technical report on the toxicology and carcinogenesis studies of 2,6-xylidine (2,6-dimethylaniline) (CAS no. 87-62-7) in Charles River CD rats (feed studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1990.

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5

Schwager, Beate. Duale Fluoreszenz: Auch bei Derivaten des 4-(9-Anthryl)-N,N-Dimethylanilins [Anthryl-N-N-Dimethylanilins]? [s.n.], 1986.

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6

Zürich, Eidgenössische Technische Hochschule, ed. Isolation and growth physiology of N, N-dimethylaniline and 2,4-dimethylaniline degrading Sphingomonas species. 1994.

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Book chapters on the topic "Dimethylaniline"

1

Gooch, Jan W. "Dimethylaniline." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3710.

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2

Schomburg, Dietmar, and Margit Salzmann. "Dimethylaniline-N-oxide aldolase." In Enzyme Handbook 1. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-86605-0_83.

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3

Schomburg, Dietmar, and Dörte Stephan. "Dimethylaniline monooxygenase (N-oxide-forming)." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_90.

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4

Wohlfarth, Ch. "Viscosity of N,N-dimethylaniline." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_290.

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5

Wohlfarth, Christian. "Viscosity of N,N-dimethylaniline." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_290.

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6

Gheorghiu, Mircea D., Mee-Kyung Chung, and Jeffrey M. Stryker. "N-tert-Butyl-3,5-Dimethylaniline." In Inorganic Syntheses: Volume 36. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118744994.ch45.

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7

Wohlfarth, Christian. "Refractive index of N,N-dimethylaniline." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_311.

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8

Wohlfarth, Ch. "Dielectric constant of the mixture (1) tetrachloromethane; (2) N,N-dimethylaniline." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_396.

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9

Wohlfarth, Ch. "Dielectric constant of the mixture (1) benzene; (2) N,N-dimethylaniline." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_943.

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10

Wohlfarth, Ch. "Dielectric constant of the mixture (1) 1,4-dimethylbenzene; (2) N,N-dimethylaniline." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_1027.

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Conference papers on the topic "Dimethylaniline"

1

Castro-Leyva, Lilia, Arturo Olivares-Perez, I. Soto-Lopez, Israel Fuentes-Tapia, and Mario Perez-Cortes. "Dimethylaniline doped as conductor polymer." In Integrated Optoelectronic Devices 2004, edited by James G. Grote and Toshikuni Kaino. SPIE, 2004. http://dx.doi.org/10.1117/12.527159.

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2

Zinth, W., S. Engleitner, and M. Seel. "Wavepacket Motion observed in an Ultrafast Electron Transfer System." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.tue.25.

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Recently it had been shown that ultrafast electron transfer (ET) reactions can occur even faster than relevant reorganisation and relaxation processes /1-3/. These experiments raised a number of new questions such as: How can those ultrafast reactions proceed, what reaction mechanism applies and what is the role of specific vibrational modes or wavepacket motions? In this paper we present new experimental results taken over a wide range of probing wavelengths with highest time resolution on a fast ET-system. We will focus on the system oxazine 1 in two solvents: The first combination is oxazin

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3

Živković, Nikola, Emila Živković, and Mirjana Kijevčanin. "Densities and viscosities of binary systems with N,N-Dimethylaniline and Tetra Ethylene Glycol Dimethyl Ether or N-Methyl-2-Pyrrolidone, as potential solvents for flue gas desulphurization processes." In 37th International Congress on Process Industry. SMEITS, 2024. http://dx.doi.org/10.24094/ptk.024.167.

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Sulfur oxides are emitted as one of the products in the process of combusting solid fossil fuels in thermal power plants, especially the Kolubara and Kostolac lignites in the Republic of Serbia. In order to reduce the emission level of the indirect Greenhouse gases (GHG) from sta-tionary sources, it is inevitable to implement flue gas desulfurization (FGD) technology. In addi-tion to the classic limestone process, technological procedures based on the physical or chemical absorption of sulfur oxides in the solvent and its thermal regeneration are becoming increasingly common. In order to prope

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4

Nagasawa, Yutaka, Arkadiy P. Yartsev, Keisuke Tominaga, and Keitaro Yoshihara. "Chemical Substitution and Deuterium Isotope Effects on Ultrafast Intermolecular Electron Transfer: Possible Role of Molecular Vibrations." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.fa.3.

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We have observed ultrafast non-exponential fluorescence quenching of 7-aminocoumarin dyes in electron donating solvents by means of femtosecond fluorescence up-conversion technique [1]. We regarded this fluorescence quenching as an ultrafast intermolecular electron transfer (ET) from the solvent to the excited dye. When the carbon chain on the amino group becomes longer, the rate of ET becomes slower, and when the amino group is fixed by hexagonal carbon ring, it becomes the slowest. Some of the fast reactions occur much faster than the diffusive solvent relaxation process. The fastest reactio

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5

Sahraoui, Bouchta, Malgorzata Makowska-Janusik, Ivan V. Kityk, Xuan Nguyen Phu, M. Salle, and A. Gorgues. "Theoretical and experimental studies of third-order nonlinear optical susceptibilities of new p-N,N'-dimethylaniline tetrathiafulvalene derivatives." In 2000 International Topical Meeting on Optics in Computing (OC2000), edited by Roger A. Lessard and Tigran V. Galstian. SPIE, 2000. http://dx.doi.org/10.1117/12.386780.

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Wynne, Klaas, C. Galli, and R. M. Hochstrasser. "Vibrational Coherence in Charge Transfer." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.tud3.

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The role of vibrational coherence in highly efficient, ultrafast electron transfer (ET) systems has recently come under investigation [1]. In the conventional theories for ET the vibrational coordinate plays an essential role: in the Sumi-Marcus theory [2] this mode facilitates ET from the excited state whereas in the Jortner-Bixon theory [3] it provides for additional decay channels in the inverted regime. In these theories it is a priori assumed that these vibrational motions are thermally equilibrated and motion along the reaction coordinate is limited by the longitudinal relaxation time of

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Kitani, A., K. Satoguchi, H. Q. Tang, and K. Sasaki. "Soluble polyanilines prepared by oxidative polymerization of dimethylanilines." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835292.

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Reports on the topic "Dimethylaniline"

1

Miller, B. Catalysis and co-catalysis of bond cleavages in coal and coal analogs. [N,N-Dimethylaniline]. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5603118.

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