Relevant bibliographies by topics / Ethanolamines

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Ethanolamines'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Ethanolamines"

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Cheng, Hua Nong, Qing Shan Liu, Bing Qiang Wang, and Shi Qing Zheng. "Reaction Kinetics of Ethanolamines with Water Catalysis." Advanced Materials Research 233-235 (May 2011): 95–100. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.95.

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An experiment of the preparation of mono-ethanolamine, die-ethanolamine, and tri-ethanolamine from aqueous ammonia and ethylene oxide is studied. In the reaction system, water carries out the catalysis. The activation energy of mono-ethanolamine is determined, 61.52kJ.mol-1. The frequency factor is a quadratic function of water concentration. Under different reaction temperature, three final ethanolamine product contents are constant, which indicate the activation energies of three ethanolamins are equal. Using nonlinear least square regression, reaction rate ratios of die-ethanolamine or tri-ethanolamine to mono-ethanolamine are calculated. The two ratios are both linear relation with water concentration, dropping with water concentration increase.
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Filburn, T., J. J. Helble, and R. A. Weiss. "Development of Supported Ethanolamines and Modified Ethanolamines for CO2Capture." Industrial & Engineering Chemistry Research 44, no. 5 (March 2005): 1542–46. http://dx.doi.org/10.1021/ie0495527.

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Labban, Abdulkarim S., and Yizhak Marcus. "Solvatochromic parameters of ethanolamines." Journal of the Chemical Society, Faraday Transactions 93, no. 1 (1997): 77–79. http://dx.doi.org/10.1039/a605521d.

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Bakalova, S., V. Mincheva, A. Doycheva, V. Groudeva, and R. Dimkov. "Microbial Toxicity of Ethanolamines." Biotechnology & Biotechnological Equipment 22, no. 2 (January 2008): 716–20. http://dx.doi.org/10.1080/13102818.2008.10817540.

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Park, Donguk, Shinbum Kim, and Kwonchul Ha. "Relationships among Fluid Ethanolamine Formulation, Airborne Ethanolamines, and Aerosol Levels in Machining Operations." Aerosol and Air Quality Research 12, no. 4 (2012): 553–60. http://dx.doi.org/10.4209/aaqr.2012.01.0002.

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Brussee, J., F. Dofferhoff, C. G. Kruse, and A. Van Der Gen. "Synthesis of optically active ethanolamines." Tetrahedron 46, no. 5 (January 1990): 1653–58. http://dx.doi.org/10.1016/s0040-4020(01)81972-4.

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Savonius, B., H. Keskinen, M. Tuppurainen, and L. Kanerva. "Occupational asthma caused by ethanolamines." Allergy 49, no. 10 (December 1994): 877–81. http://dx.doi.org/10.1111/j.1398-9995.1994.tb00791.x.

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Wichmann, M., and M. Stockhausen. "Dielectric Relaxation of Three Ethanolamines." Zeitschrift für Naturforschung A 56, no. 8 (August 1, 2001): 603–4. http://dx.doi.org/10.1515/zna-2001-0811.

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Abstract Relaxation spectra have been measured at 20°C for mono-, di-and triethanolamine in the pure liquid state and in a 0.6 mole fraction mixture with 1,4-dioxane. The general resemblance to the dielectric behaviour of alcohols and aminoalcohols shows that relaxation is governed by association effects. In this regard, several features point to significantly differing behaviour of the mono compound in comparison with both di-and triethanol­ amine.
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DiGuilio, Ralph M., William L. McGregor, and Amyn S. Teja. "Thermal conductivities of the ethanolamines." Journal of Chemical & Engineering Data 37, no. 2 (April 1992): 242–45. http://dx.doi.org/10.1021/je00006a029.

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T. Vashi, R., H. M. Bhajiwala, and S. A. Desai. "Ethanolamines as Corrosion Inhibitors for Zinc in (HNO3+H2SO4) Binary Acid Mixture." E-Journal of Chemistry 7, no. 2 (2010): 665–68. http://dx.doi.org/10.1155/2010/518543.

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This work deals with the study of corrosion behaviour for zinc in (HNO3+ H2SO4) binary acid mixture containing ethanolamines. Corrosion rate increases with concentration of acid and temperature. At constant acid concentration, the inhibition efficiency of ethanolamines increases with the inhibitor concentration. Value of ΔGa increases and inhibition decreases with temperature. The mode of inhibition action appears to be chemisorption.
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Dissertations / Theses on the topic "Ethanolamines"

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Ridgway, Neale David. "Rat hepatic phosphatidylethanolamine N-methyltransferase : enzyme purification and characterization." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/29377.

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Phosphatidylethanolamine (PE) N-methyltransferase catalyzes the stepwise transfer of methyl groups from S-adenosyl-L-methionine (AdoMet) to the amino headgroup of PE. Successive methylation results in the formation of the two intermediates, phosphatidyl-N-monomethylethanolamine (PMME) and phosphatidyl-N, N-dimethylethanolamine (PDME), and the final product phosphatidylcholine (PC). PE N-methyltransferase is an integral membrane protein localized primarily in the endoplasmic reticulum (microsomal fraction) of liver. PE-, PMME- and PDME-dependent PE N-methyltransferase activities were purified from Triton X-100 solubilized microsomes 429-, 1542- and 832-fold, respectively. The purified enzyme was composed of a single 18.3 kDal protein as determined by SDS-PAGE. Molecular mass analysis of purified PE N-methyltransferase (in Triton X-100 micelles) by gel filtration on Sephacryl S-300 indicated the enzyme existed as a 24.7 kDal monomer. PE N-methyltransferase catalyzed the complete conversion of PE to PC and had a pH optimum of 10 for all three steps. A Triton X-100 mixed micelle assay was developed to assay PE-, PMME- and PDME-dependent activities of both pure and microsomal PE N-methyltransferase. The AT-terminal amino acid sequence of rat liver PE N-methyltransferase and the recently cloned 23.1 kDal S. cerevisiae PEM 2 were found to be 35% homologous. Double reciprocal plots for PE N-methyltransferase at fixed Triton X-100 concentrations and increasing PE, PMME or PDME were highly cooperative. Similar cooperative effects were noted when phospholipid was fixed and Triton X-100 increased. The cooperativity could be partially abolished if a fixed mol% of nonsubstrate phospholipid such as PC was included in the assay. This would indicate that PE N-methyltransferase has specific binding requirements for a site(s) in contact with the micellar substrate. The occupation of this boundary layer by phospholipid is essential for full expression of enzyme activity. Kinetic analysis revealed that PMME and PDME methylation followed an ordered Bi-Bi mechanism. The overall mechanism involves initial binding of PE to a common site and successive methylation steps involving the binding and release of AdoMet and S-adenosyl-L-homocysteine, respectively. Cysteine residue(s) (which are rapidly oxidized in the absence of reduced thiols) are involved in the catalytic mechanism. Reverse-phase HPLC was used to fractionate the phospholipid products of PE N-methyltransferase into individual molecular species. Substrate specificity experiments on PE N-methyltransferase in vitro and in vivo revealed no selectivity for any molecular species of diacyl PE, PMME or PDME. The PE-derived PC, which is rich in 16:0-22:6, is rapidly remodeled to conform to the molecular species compositon of total hepatocyte PC in vivo . The 18.3 kDal PE N-methyltransferase was found to be a substrate for cAMP-dependent protein kinase in vitro. However, only 0.25 mol phosphorus/mol of PE Af-methyltransferase was incorporated, with no observed effect on activity. Studies on PE N-methyltransferase regulation in choline-deficient rat liver indicated that activity changes were due to elevated levels of cellular PE. Immunoblotting of choline-deficient liver microsomes or hepatocyte membranes with a anti-PE N-methyltransferase antibody revealed no alteration in enzyme mass. While more work is needed, initial indications are that hepatic PE N-methyltransferase is a constitutive enzyme regulated primarily by substrate and product levels.
Medicine, Faculty of
Biochemistry and Molecular Biology, Department of
Graduate
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Merelli, Bérangère. "Proinsecticides chiraux d'acides carboxyliques et de β-ethanolamines : effet de la chiralité sur la métabolisation et les activités biologiques chez l'insecte." Versailles-St Quentin en Yvelines, 2004. http://www.theses.fr/2004VERS0005.

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Les D2-thiazolines et les N-acylaziridines sont étudiées comme structures de proinsecticides d'acides carboxyliques fluorés ou non. Les D2-thiazolines ont été obtenues sous forme de racémiques et d'énantiomères purs par une méthode de thionation/cyclisation en utilisant le réactif de Lawesson. Les N-acylaziridines ont été synthétisées en condensant un acide carboxylique sur une aziridine obtenue sous forme racémique et énantiomériquement pure à partir d'oxiranes. Des méthodes d'analyse chirale de RMN et HPLC ont été mises au point sur les différents substrats synthétisés pour contrôler la pureté énantiomérique et pour évaluer la composition d'extraits de milieux biologiques d'insectes incubés par des racémiques de N-acylaziridines suite à une hydrolyse enzymatique incomplète. Les propriétés biologiques des D2-thiazolines et des N-acylaziridines ont été évaluées au cours de tests effectués sur Drosophile, Puceron ou Acarien. La métabolisation des molécules les plus intéressantes a été étudiée en présence de milieu biologique d'insecte (tissus de criquet ou de chenille ou a-chymotrypsine), sans prétraitement de l'échantillon, par RMN 19F ou par HPLC avec injection directe sur des colonnes large pore et des colonnes monolithiques. En présence de ces milieux biologiques, les N-acylaziridines étudiées se comportent effectivement comme des proinsecticides d'acides carboxyliques puisqu'elles le démasquent efficacement. Les D2-thiazolines se révèlent plus stables puisqu'elles nécessitent l'utilisation de milieux biologiques concentrés pour libérer une faible quantité d'acide carboxylique
The nitrogen heterocylces D2-thiazoline and N-acylaziridine were studied as potential proinsecticides masking the active principles : fluorinated or not carboxylic acids. The synthesis of D2-thiazolines, either as racemates or as pure enantiomers, were performed by thionation/cyclisation using Lawesson reagent. The synthesis of N-acylaziridines were performed by condensation of carboxylic acid with amine obtained as racemate and as pure enantiomer using oxiranes. We developped analytical chiral methods of NMR and HPLC to verify optical purity of different substrates. Then, these methods were applied to extracts of incubated insect tissues by N-acylaziridines racemates after a partial unmasking for the determination of the enantiomeric composition. The biological properties of these potentials proinsecticides were evaluated by several testings performed with various pests : Drosophila melanogaster, Aphis gossypii, Myzus persicae, Tetranychus urticae. The metabolization of the most interesting molecules was studied in insect biological media (tissues of locusts or caterpillars or with a-chymotrypsin), without any pretreatment, using analytical methods such as 19F[1H]NMR or HPLC allowing the direct injection on particular packing material such as wide pore particles or monolithic column. In these biological media, N-acylaziridines beleave effectively as proinsecticides of the carboxylic acid, since the unmasking is very efficient. D2-thiazolines are more stable since it's necessary to use concentred biological media for unmasking a little of active principle
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Vadapalli, Vatsala. "Role of N-Acylethanolamines in Plant Defense Responses: Modulation by Pathogens and Commercial Antimicrobial Stressors." Thesis, University of North Texas, 2010. https://digital.library.unt.edu/ark:/67531/metadc30521/.

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N-acyl ethanolamines (NAEs) are a class of lipids recently recognized as signaling molecules which are controlled, in part, by their degradation by fatty acid amide hydrolase (FAAH). On the basis of previous studies indicating increased NAE levels in a tobacco cell suspension-xylanase elicitor exposure system and the availability of FAAH mutants, overexpressor and knockout (OE and KO) genotypes in Arabidopsis thaliana, further roles of NAEs in A. thaliana plant defense was investigated. The commonly occurring urban antimicrobial contaminant triclosan (TCS) has been shown to suppress lipid signaling associated with plant defense responses. Thus, a second objective of this study was to determine if TCS exposure specifically interferes with NAE levels. No changes in steady state NAE profiles in A. thaliana-Pseudomonas syringae pv. syringae and A. thaliana-flagellin (bacterial peptide, flg22) challenge systems were seen despite evidence that defense responses were activated in these systems. There was a significant drop in enoyl-ACP reductase (ENR) enzyme activity, which catalyzes the last step in the fatty acid biosynthesis pathway in plants, on exposure of the seedlings to TCS at 10 ppm for 24 h and decreased reactive oxygen species (ROS) production due to flg22 in long term exposure of 0.1 ppm and short term exposure of 5 ppm. However, these responses were not accompanied by significant changes in steady state NAE profiles.
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Lewis, C. J. "Ethanolamine metabolism in yeasts." Thesis, University of Liverpool, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384437.

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Ashagbley, Anthony J. "Ethanolamine requirement and cell proliferation." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq23203.pdf.

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Kilaru, Aruna. "Role of Fatty Acid Ethanolamides in Plants." Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etsu-works/4767.

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Gibellini, Federica. "The ethanolamine branch of the Kennedy pathway in Trypanosoma brucei." Thesis, University of Dundee, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.510655.

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Sibomana, Isaie. "Evidence That Myo-Inositol Plus Ethanolamine Elevates Plasmalogen Levels And Lends Protection Against Oxidative Stress In Neuro-2A Cells." Wright State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=wright1484661880801698.

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Kilaru, Aruna. "Fatty Acid Ethanolamide Metabolism Influences Growth and Stress Responses." Digital Commons @ East Tennessee State University, 2014. https://dc.etsu.edu/etsu-works/4773.

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Sriparameswaran, Anuja. "Subcellular Localization of N-acylphosphatidyl-ethanolamine Synthase in Cotyledons of Cotton Seedlings." Thesis, University of North Texas, 1995. https://digital.library.unt.edu/ark:/67531/metadc278717/.

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N-acylation of phosphatidylethanolamine (PE) with free fatty acids catalyzed by N-acyl phosphatidylethanolamine (NAPE) synthase was reported in cotyledons of 24-h-old cotton seedlings. Here I report subcellular localization of this enzyme. Differential centrifugation, sucrose density gradient fractionation,aqueous two-phase partitioning and electron microscopy techniques were utilized to elucidate subcellular site(s) of NAPE synthase. Marker enzymes were used to locate organelles in subcellular fractions. Differential centrifugation indicated that NAPE synthase is present in more than one organelle and it is a membrane bound enzyme. Sucrose density gradient fractionations indicated that NAPE synthase is present in membranes derived from endoplasmic reticulum (ER),Golgi and possibly plasma membrane (PM) but not mitochondria, glyoxysomes or plastids. Aqueous two-phase partitioning experiments with cotton and spinach tissues supported these results but Goigi appeared to be the major site of NAPE synthesis. Electron microscopy of subcellular fractions was used to examine isolated fractions to provide visual confirmation of our biochemical results. Collectively, these results indicate that NAPE is synthesized in plant ER, Golgi and possibly PM.
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Books on the topic "Ethanolamines"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 2-aminoetanōru: 2-aminoethanol. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Zech, Ronald. Entgiftung von Organophosphaten durch Phosphorylphosphatasen und Ethanolamin. Bonn: Bundesverwaltungsamt, Zentralstelle für Zivilschutz, 2001.

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Arpe, Edited by: H. J. Ethanolamines and Propanolamines to Fiber, 4, Synthetic Organic, Volume A10, Ullmann's Encyclopedia of Industrial Chemistry. 5th ed. Wiley-VCH, 1987.

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Ullmann's Encyclopedia of Industrial Chemistry, Vol A1O: Ethanolamines to Fibers, 4, Synthetic Organic (Ullmann's Encyclopedia of Industrial Chemistry 5th ed Vol a). 5th ed. Vch Pub, 1988.

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1943-, Sybrecht Gerhard, and World Congress of Asthmology (12th : 1987 : Barcelona, Spain), eds. Formoterol, a new long-acting bronchodilator: An international symposium held during the XIIth World Congress of Asthmology, Barcelona, 1987. Toronto: Hans Huber Publishers, 1988.

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J, Davies Robert, and European Society of Pneumology. Congress, eds. Formoterol: Clinical profile of a new long-acting inhaled [beta]2-agonist : an international symposium held during the VIIth Congress of the European Society of Pneumology (SEP), Budapest, 1988. Toronto: Hogrefe & Huber, 1990.

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Davies, R. J. Formoterol - Clinical Profile of a New Long -. Hogrefe & Huber Publishers, 1991.

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Blokdijk, G. J. Ethanolamine Oleate; The Ultimate Step-By-Step Guide. CreateSpace Independent Publishing Platform, 2018.

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COM (93) 535 Final, Brussels, 8 November 1993: Proposal for a Council Regulation (EEC) Extending the Provisional Anti-dumping Duty on Imports of Ethanolamines ... (93) 535 Final, Brussels, 8 November 1993). European Communities / Union (EUR-OP/OOPEC/OPOCE), 1993.

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1946-, Barnes Peter J., Matthys Heinrich, and European Society of Pneumology. Congress, eds. Formoterol--a new-generation [beta] 2-agonist: An international symposium held during the 8th Congress of the European Society of Pneumology, Freiburg, Federal Republic of Germany, September 1989. Toronto: Hogrefe & Huber, 1991.

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Book chapters on the topic "Ethanolamines"

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Reiter, L. G., V. A. Potaskalov, A. A. Andriiko, V. S. Kublanovsky, M. A. Chmilenko, Yu K. Pirskiy, V. I. Lisin, and S. M. Chmilenko. "ELECTROCHEMICAL ACTIVITY OF CARBONS MODIFIED BY d-METAL COMPLEXES WITH ETHANOLAMINES." In New Carbon Based Materials for Electrochemical Energy Storage Systems: Batteries, Supercapacitors and Fuel Cells, 333–44. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4812-2_26.

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Gooch, Jan W. "Ethanolamine." In Encyclopedic Dictionary of Polymers, 275. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4528.

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Bährle-Rapp, Marina. "Ethanolamine." In Springer Lexikon Kosmetik und Körperpflege, 191. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3688.

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Bährle-Rapp, Marina. "Ethanolamine Dithiodiglycolate." In Springer Lexikon Kosmetik und Körperpflege, 191. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3689.

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Bährle-Rapp, Marina. "Ethanolamine Glycerophosphate." In Springer Lexikon Kosmetik und Körperpflege, 191. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3690.

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Bährle-Rapp, Marina. "Ethanolamine HCL." In Springer Lexikon Kosmetik und Körperpflege, 191. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3691.

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Bährle-Rapp, Marina. "Ethanolamine Thioglycolate." In Springer Lexikon Kosmetik und Körperpflege, 191. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3692.

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Schomburg, Dietmar, and Dörte Stephan. "Ethanolamine kinase." In Enzyme Handbook 13, 1009–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59176-1_191.

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Bährle-Rapp, Marina. "Stearamidoethyl Ethanolamine." In Springer Lexikon Kosmetik und Körperpflege, 528. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9991.

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Schomburg, Dietmar, Margit Salzmann, and Dörte Stephan. "Ethanolamine oxidase." In Enzyme Handbook, 849–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-58051-2_173.

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Conference papers on the topic "Ethanolamines"

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Gunji, Takahiro, Daijiroh Mori, Tsuyoshi Sugita, Koji Arimitsu, Yoshimoto Abe, and Kazuhiro Sayama. "Preparation and Characterization of BiVO4 Semiconductor Thin Film by Precursor Method using Ethanolamines." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1114-g08-09.

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Jiang, Wei, and Ziyuan Li. "PREPARATION AND STUDY OF PROPERTIES OF DI(TRIMETHYLOLPROPANE) BIPHOSPHATE ETHANOLAMINE SALT." In International Conference on New Materials and Intelligent Manufacturing. Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.12.15.

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Muresan, Vlad, Mihail Abrudean, Tiberiu Colosi, Zoltan Kovendi, Mihaela-Ligia Unguresan, and Iulia Clitan. "Modeling and Simulation of the Carbone Dioxide Absorption Process in Ethanolamine Solution." In 2015 20th International Conference on Control Systems and Computer Science (CSCS). IEEE, 2015. http://dx.doi.org/10.1109/cscs.2015.121.

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Denisenko, Y., T. Novgorodtseva, E. Ermolenko, A. Prikhodko, J. Perelman, S. Kasynov, and R. Sultanov. "Blood Plasma Molecular Species of Ethanolamine Plasmalogens in Asthma Complicated with Obesity." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a4320.

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Xin, Li, Wang Huan, Liu Li-Ye, Zhang Ji-Bo, and Qiu Jun. "PREPARATION AND CHARACTERIZATION OF CATALYST FOR REDUCTION AMINATION OF ETHANOLAMINE BY DIFFERENT METHOD." In International Conference on New Materials and Intelligent Manufacturing (ICNMIM). Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.239.242.

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Xiao, Min, Dong Liang, Hao Shena, Jian-Yong Liu, and Hai-Yan Li. "Research on the Production Reaction Kinetics and Thermochromism of Salicylaldehyde Ethanolamine Schiff Base." In 2014 7th International Conference on Intelligent Computation Technology and Automation (ICICTA). IEEE, 2014. http://dx.doi.org/10.1109/icicta.2014.148.

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Teramae, Hiroyuki, and Yasuko Y. Maruo. "Theoretical study on the structures of ethanolamine and its water complexes using the Hamiltonian algorithm." In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2015 (ICCMSE 2015). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938849.

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Li, C., X. Pei, F. Zheng, K. Cao, and D. Ren. "Niclosamide Ethanolamine Salt Attenuated Idiopathic Pulmonary Fibrosis by Suppresses TGF-β1 Mediated Epithelial-Mesenchymal Transition." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a4053.

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Southwick, Jeffrey, Mark Brewer, Diederik van Batenburg, Sebastiaan Pieterse, Ron Bouwmeester, Dawood Mahruqi, Abdullah Alkindi, and Rifaat Mjeni. "Ethanolamine as Alkali for Alkali Surfactant Polymer Flooding - Development of a Low-Complexity Field Implementation Concept." In SPE Improved Oil Recovery Conference. Society of Petroleum Engineers, 2020. http://dx.doi.org/10.2118/200432-ms.

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Shah, Tariq, Balaji Krishnamachary, Flonne Wildes, Jannie Wijnen, Kristine Glunde, and Zaver M. Bhujwalla. "Abstract 1195: Ethanolamine kinase-1 and phosphoethanolamine are potential diagnostic markers and therapeutic targets in breast cancer." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1195.

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Reports on the topic "Ethanolamines"

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Owens, J., A. Vu, and C. Koester. Analysis of Ethanolamines: Validation of Semi-Volatile Analysis by HPLC-MS/MS by EPA Method MS888. Office of Scientific and Technical Information (OSTI), October 2008. http://dx.doi.org/10.2172/945589.

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You might also be interested in the extended bibliographies on the topic 'Ethanolamines' for particular source types:
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