Relevant bibliographies by topics / Dinitrosalicylic acid

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Dinitrosalicylic acid'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dinitrosalicylic acid"

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Senthil Kumar, V. S., Srinivasan S. Kuduva, and Gautam R. Desiraju. "Pseudopolymorphs of 3,5-dinitrosalicylic acid." Journal of the Chemical Society, Perkin Transactions 2, no. 6 (1999): 1069–74. http://dx.doi.org/10.1039/a902134e.

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Senthil Kumar, V. S., Srinivasan S. Kuduva, and Gautam R. Desiraju. "3,5-Dinitrosalicylic acid-phenazine (1/1)." Acta Crystallographica Section E Structure Reports Online 58, no. 8 (2002): o865—o866. http://dx.doi.org/10.1107/s1600536802012473.

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Xu, Hui, Yanjun Tian, Kunfu Zhu, et al. "A New Quantitative Determination Method of Acetoin." International Journal of Current Microbiology and Applied Sciences 11, no. 3 (2022): 80–85. http://dx.doi.org/10.20546/ijcmas.2022.1103.010.

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To obtain a new quantitative determination method of Acetoin for reducing the cost of testing and the workload in the process of strain breeding. In an alkaline environment, using 3,5-dinitrosalicylic acid with strong oxidizing properties to azeotrope with Acetoin, 3,5-dinitrosalicylic acid is reduced to 3-amino-5-nitrosalicylic acid and 3-amino-5-nitrosalicylic acid are red-brown substances. The content of Acetoin can be obtained by detecting the absorbance at 540 nm. This new quantitative determination method of Acetoin is a simple, rapid and low-cost method for quantitative determination of
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Wang, Guangyi, Themis J. Michailides, and Richard M. Bostock. "Improved Detection of Polygalacturonase Activity due to Mucor piriformis with a Modified Dinitrosalicylic Acid Reagent." Phytopathology® 87, no. 2 (1997): 161–63. http://dx.doi.org/10.1094/phyto.1997.87.2.161.

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An assay for determination of galacturonic acid with 3,5-dinitrosalicylic acid was developed that substantially extends the linear range of detection compared to a previously published method with this reagent. In the improved assay, galacturonic acid was detected with a reagent containing 44 mM 3,5-dinitrosalicylic acid, 4 mM sodium sulfite, and 375 mM sodium hydroxide. The absorbance of the solution after reaction with galacturonic acid was determined at 575 nm and was linear at concentrations of galacturonic acid up to 50 μmol, with a lower limit of detection at ~400 nmol. The assay with th
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Essawy, A. A. I., and M. S. A. Abdel-Mottaleb. "Photosensitized degradation of dinitrosalicylic acid by uranyl ions." International Journal of Photoenergy 5, no. 4 (2003): 219–21. http://dx.doi.org/10.1155/s1110662x03000357.

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The photodegradation of dinitrosalicylic acid (DNS) by photoexcited uranyl ion was studied in aqueous solutions. The failure of DNS to degrade directly with light highlights the importance of the photoexcited uranyl ion in controlling the photochemical processes. Fluorescence quenching studies showed that an electron-transfer process from the DNS to the excited uranyl ion is involved leading to the formation ofUO2+/DNS•+radical pair complex as an initial step. Illumination of theUO22+/DNS solution in presence of oxygen results in mineralization of DNS. The results are explained on the basis of
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Madaj, Rafał, Halina Kalinowska, Witold Sroczyński, Jakub Szeląg, and Elżbieta Sobiecka. "Biodegradation of 3,5-dinitrosalicylic acid by Phanerochaete chrysosporium." Folia Biologica et Oecologica 14 (December 30, 2018): 14–22. http://dx.doi.org/10.1515/fobio-2017-0005.

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Despite intensive efforts put on prevention of environment pollution by nitroaromatic compounds, these xenobiotics have not been eliminated from the biosphere. The physicochemical properties make nitroaromatics extremely recalcitrant to biodegradation. Therefore, microbial degraders of these pollutants are sought after. This paper reports preliminary results of the study on degradation of 3,5-dinitrosalicylic acid (DNS) by a basidiomycetous fungus Phanerochaete chrysosporium under stationary conditions in a culture medium containing 0.05–0.5% v/v of DNS. The results obtained suggest that the f
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Gonçalves, Cristiana, Rosa Maria Rodriguez-Jasso, Nelma Gomes, José A. Teixeira, and Isabel Belo. "Adaptation of dinitrosalicylic acid method to microtiter plates." Analytical Methods 2, no. 12 (2010): 2046. http://dx.doi.org/10.1039/c0ay00525h.

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Smith, Graham, Urs D. Wermuth, Peter C. Healy, and Jonathan M. White. "Structure-Making with 3,5-Dinitrosalicylic Acid. II. The Proton-Transfer Compounds of 3,5-Dinitrosalicylic Acid with the Monocyclic Heteroaromatic Amines." Australian Journal of Chemistry 56, no. 7 (2003): 707. http://dx.doi.org/10.1071/ch02163.

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The crystal structures of the proton-transfer compounds of 3,5-dinitrosalicylic acid (dnsa) with a series of common monocyclic heteroaromatic amines (pyridine, 4-cyanopyridine, pyridine-4-carboxylic acid, 2,6-diaminopyridine, and 2-aminopyrimidine) have been determined and the hydrogen-bonding associations in each analyzed. The compounds are the adduct [(C5H6N)+(dnsa)–· (dnsa)] (1), the 1 : 1 salts [(C6H5N2)+(dnsa)–] (2), [(C6H6NO2)+(dnsa)–] (3), [(C5H8N3)+(dnsa)–] (4), and the 2 : 2 ethanol hemi-solvate [2(C4H6N3)+·2(dnsa)–· 0.5(EtOH)] (5). With all compounds, protonation of the hetero-nitrog
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Madaj, Rafał, Witold Sroczyński, Michał Sójka, Tomasz P. Olejnik, and Elżbieta Sobiecka. "Batch Mode Reactor for 3,5-Dinitrosalicylic Acid Degradation by Phanerochaete chrysosporium." Processes 9, no. 1 (2021): 105. http://dx.doi.org/10.3390/pr9010105.

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A new batch mode reactor was constructed to conduct continuous biodegradation of 3,5-dinitrosalicylic acid. Various types of matrices with immobilized Phanerochaete chrysosporium were immersed in a solution containing pollutant and mineral nutrients. Three parameters were chosen to optimize the process. The nitrate and nitrite ions concentrations and HPLC analysis were used to prove the biodegradation of 3,5-dinitrosalicylic acid, and the mixed effects model using one-factor ANOVA was used for statistical calculations. The results showed the correlation between the initial pH, a medium composi
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Xia, Meng-lei, Lan Wang, Zhi-xia Yang, and Hong-zhang Chen. "A novel digital color analysis method for rapid glucose detection." Analytical Methods 7, no. 16 (2015): 6654–63. http://dx.doi.org/10.1039/c5ay01233c.

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Dissertations / Theses on the topic "Dinitrosalicylic acid"

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Yee, Melinda Chua Fui. "An investigation of the biology and chemistry of the Chinese medicinal plant, Amorphophallus konjac." Thesis, University of Wolverhampton, 2011. http://hdl.handle.net/2436/237603.

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Konjac glucomannan (KGM), the main biologically active constituent of konjac flour extracted from corms of Amorphophallus konjac (konjac), can be used to prepare functional foods and may also have potential as a pharmaceutical product to combat obesity. The current study employed three experimental approaches to study the biology and chemistry of konjac, namely (1) glasshouse experiments to study the morphogenesis, growth and productivity of konjac plants, (2) a histological and immunocytochemical investigation of the localisation and developmental regulation of the deposition and metabolism o
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Book chapters on the topic "Dinitrosalicylic acid"

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Jain, Aakanchha, Richa Jain, and Sourabh Jain. "Quantitative Analysis of Reducing Sugars by 3, 5-Dinitrosalicylic Acid (DNSA Method)." In Basic Techniques in Biochemistry, Microbiology and Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-4939-9861-6_43.

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Li, He, and Lauren S. McKee. "Measuring Enzyme Kinetics of Glycoside Hydrolases Using the 3,5-Dinitrosalicylic Acid Assay." In Methods in Molecular Biology. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3151-5_2.

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McKee, Lauren S. "Measuring Enzyme Kinetics of Glycoside Hydrolases Using the 3,5-Dinitrosalicylic Acid Assay." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6899-2_3.

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Sarkar, Mrittika, Anshika Sah, Payal Agarwal, Sai Joshi, and Sinchan Hait. "Quantification Tests for Carbohydrate Detection." In Practical Biochemistry. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815165852124010006.

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Quantification of carbohydrates by the anthrone method is a colourimetric assay. In this method, first, the complex carbohydrates are hydrolysed in a highly acidic medium, resulting in monosaccharides. Thereafter, these monosaccharides are dehydrated to form 5-hydroxymethylfurfural (5-HMF) or 2-furfural (2-F), followed by reacting with anthrone reagent. This reaction produces a blue-green complex which is colourimetrically determined. In DNSA method 3,5-dinitrosalicylic acid (DNSA), a yellow colour reagent reacts with reducing sugar’s carbonyl group and forms orangered colour compound 3-Amino-
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Aruna, B., and Aarthi Kunwar Rathore. "ANTIBACTERIAL EFFECT OF TANNASE PRODUCING BACTERIA - ISOLATED FROM GOAT FAECAL SAMPLE." In Futuristic Trends in Agriculture Engineering & Food Sciences Volume 3 Book 16. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bcag16p1ch1.

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The faecal samples of goat were used to isolate tannase producing bacteria.The tannase producing isolates (T1 and T2) were identified as Corynebacterium xerosis and Coryne bacterium kutser. The tannase activity found to be,15.2 U/mL (T1 isolate) and 16.5 U/mL (T2) at 37oC; 16.2 U/mL (T1) and 16.1 U/mL (T2) at pH 8by using tannin as asubstrate.The tannase activity was maximum at 37oC and pH 8. The activity of Tannase of the isolates was confirmed by detection of gallic acidby TLC (Thin layer chromatography) and glucose by DNS (3, 5-Dinitrosalicylic acid) method. The T2 Tannase showed antibacter
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Conference papers on the topic "Dinitrosalicylic acid"

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Afroz, Ziya, Mohammad Jane Alam, Zulkarnain, Mohd Faizan, Afaq Ahmad, and Shabbir Ahmad. "DFT and TD-DFT computation of charge transfer complex between o-phenylenediamine and 3,5-dinitrosalicylic acid." In DAE SOLID STATE PHYSICS SYMPOSIUM 2015. Author(s), 2016. http://dx.doi.org/10.1063/1.4948002.

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Schechner, Pinchas, Eugenia Bubis, and Lea Mor. "Glucose Fueled Alkaline Fuel Cell." In ASME 2005 3rd International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2005. http://dx.doi.org/10.1115/fuelcell2005-74029.

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The electrical behavior of a room temperature membraneless Alkaline Fuel Cell, with incorporated platinum particles in the anode and fueled with glucose, is reported. The Open Circuit Voltage, at different initial glucose concentrations was measured. Changes on the glucose concentration with time were monitored with the dinitrosalicylic acid method. Qualitative Thin Layer Chromatography demonstrates that the electrodes induce polymerization of the glucose. The electrical yield of the system was measured with different external resistors. The Open Circuit Voltage reaches a saturation value of 0
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You might also be interested in the extended bibliographies on the topic 'Dinitrosalicylic acid' for particular source types:
Journal articles
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