Relevant bibliographies by topics / Triazone

Contents

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

Academic literature on the topic 'Triazone'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Triazone"

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Clapp, J. G. "Foliar Application of Liquid Urea-triazone-based Nitrogen Fertilizers and Crop Safety." HortTechnology 3, no. 4 (1993): 442–44. http://dx.doi.org/10.21273/horttech.3.4.442.

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Urea-triazone-based nitrogen (N) solutions were evaluated for potential leaf injury on agronomic and horticultural crops at 61 commercial grower sites throughout the United States. Poliar spray solutions containing triazone N were used at concentrations ranging from 1.5% to 15.7%. Safe N concentrations for urea-triazone-based N products ranged from 1.5% for crops such as sweet corn, apple, cherry, and pear, and up to 15.7% for nursery root stocks. Urea-triazone-based N solutions were found to be much safer on crop foliage than ammonium-, nitrate-, and/or all urea-based foliar fertilizer produc
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Clapp, John G. "Urea-Triazone N Characteristics and Uses." Scientific World JOURNAL 1 (2001): 103–7. http://dx.doi.org/10.1100/tsw.2001.356.

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Urea-triazone nitrogen (N) is a stable solution resulting from a controlled reaction in aqueous medium of urea, formaldehyde, and ammonia which contains at least 25% total N. This N source contains no more than 40%, nor less than 5%, of total N from unreacted urea and not less that 40% from triazone. All other N shall be derived from water-soluble dissolved reaction products of the above reactants. It is a source of slowly available N. The rate of mineralization of urea-triazone is about 66% that of urea after 8 days when incorporated in a Munjor sandy loam. Ammonia volatilization losses of N
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Tsuchiya, Takumi, Azusa Kikuchi, Nozomi Oguchi-Fujiyama, Kazuyuki Miyazawa, and Mikio Yagi. "Photoexcited triplet states of UV-B absorbers: ethylhexyl triazone and diethylhexylbutamido triazone." Photochemical & Photobiological Sciences 14, no. 4 (2015): 807–14. http://dx.doi.org/10.1039/c4pp00373j.

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The lowest excited triplet state of a UV-B absorber with extremely high molecular extinction, ethylhexyl triazone, can be assigned to a locally excited<sup>3</sup>ππ* state within a chromophore,p-(N-methylamino)benzoic acid.
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Teixeira, Walquíria F., Evandro B. Fagan, Antônio P. M. Machado, Daniel Fortune, and Fernando R. Moreira. "Foliar Application of Nitrogen Affects Metabolism and Productivity of Soybean." Journal of Agricultural Science 13, no. 10 (2021): 31. http://dx.doi.org/10.5539/jas.v13n10p31.

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Soybean is one of the world&amp;rsquo;s most economically important crops and several factors can affect the productivity of this culture. Among these factors is the supply of needed nitrogen, especially in the reproductive stage, as it acts in photosynthetic activity and in grain filling. In view of this, the objective of our work was to evaluate the effect of foliar application of nitrogen in different reproductive stages in soybean culture. Two sources of nitrogen were used: conventional urea and urea-formaldehyde/triazone, both applied in reproductive stages R2, R3, R4, or R5, as well as a
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Thorel, Evane, Fanny Clergeaud, Lucie Jaugeon, et al. "Effect of 10 UV Filters on the Brine Shrimp Artemia salina and the Marine Microalga Tetraselmis sp." Toxics 8, no. 2 (2020): 29. http://dx.doi.org/10.3390/toxics8020029.

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The presence of pharmaceutical and personal care product (PPCP) residues in the aquatic environment is an emerging issue due to their uncontrolled release through gray water, and accumulation in the environment that may affect living organisms, ecosystems and public health. The aim of this study is to assess the toxicity of benzophenone-3 (BP-3), bis-ethylhexyloxyphenol methoxyphenyl triazine (BEMT), butyl methoxydibenzoylmethane (BM), methylene bis-benzotriazolyl tetramethylbutylphenol (MBBT), 2-ethylhexyl salicylate (ES), diethylaminohydroxybenzoyl hexyl benzoate (DHHB), diethylhexyl butamid
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Pathak, Suraj Kumar, Yepeng Xiang, Manli Huang, et al. "Fused tetracyclic tris[1,2,4]triazolo[1,3,5]triazine as a novel rigid electron acceptor for efficient thermally activated delayed fluorescence emitters." RSC Advances 10, no. 26 (2020): 15523–29. http://dx.doi.org/10.1039/d0ra01925a.

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Zeng, Qun, Yanyang Qu, Jinshan Li, and Hui Huang. "Theoretical studies on the derivatives of tris([1,2,4]triazolo)[4,3-a:4′,3′-c:4′′,3′′-e][1,3,5]triazine as high energetic compounds." RSC Advances 6, no. 7 (2016): 5419–27. http://dx.doi.org/10.1039/c5ra22524h.

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Cassim, Bruno Maia Abdo Rahmen, Antonio Pedro Martins Machado, Daniel Fortune, Fernando Rodrigues Moreira, Éder Júnior De Oliveira Zampar, and Marcelo Augusto Batista. "Effects of Foliar Application of Urea and Urea-Formaldehyde/Triazone on Soybean and Corn Crops." Agronomy 10, no. 10 (2020): 1549. http://dx.doi.org/10.3390/agronomy10101549.

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The objective of the study was to evaluate the effect of foliar application of urea and urea-formaldehyde, triazone-based fertilizers on soybean and corn crops. Four experiments were carried out, two on soybeans, one on first season corn, and the other on second season corn. The experiments were conducted using a randomized block design, with 5 treatments studied: T1—control without application of foliar nitrogen (N); T2—foliar application of conventional urea solution and three treatments with Hexion foliar fertilizers based on urea-formaldehyde and triazone (N-Hexion®), with varying levels o
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Sommer, S., S. M. Wilkinson, J. S. C. English, and J. Ferguson. "Photoallergic contact dermatitis from the sunscreen octyl triazone." Contact Dermatitis 46, no. 5 (2002): 304–5. http://dx.doi.org/10.1034/j.1600-0536.2002.460514.x.

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Ricci, Andrea, Michelle N. Chrétien, Abdelhamid Sayari, and J. C. Scaiano. "Photophysical Properties of Methyl Triazone Included in MCM-41¶." Photochemistry and Photobiology 81, no. 4 (2005): 949. http://dx.doi.org/10.1562/2005-03-19-rn-466r.1.

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Dissertations / Theses on the topic "Triazone"

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Wright, Glenn C., and Marco A. Peña. "Use of a Slow Release Triazone-Based Nitrogen Fertilizer on Lemon Trees." College of Agriculture, University of Arizona (Tucson, AZ), 2000. http://hdl.handle.net/10150/223855.

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Trisert CB replaced conventional foliar applied low-biuret urea and liquid urea ammonium nitrate in a typical N fertilization regime, a urea triazone based N source. There was no yield decrease, change in fruit size or grade with the use of the Trisert CB. There were no differences in leaf P, K, Ca, Mg, Cu, Fe, Mn or Zn concentration. Occasionally, leaf N concentration of trees supplied with foliar applied Trisert CB was higher than that of the control treatment.
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Glowacki, Aurore. "Synthèse de nouveaux dérivés d’hydrazine pour la propulsion spatiale." Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE1187.

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Ce travail est dédié à la synthèse de composés polyazotés linéaires (N-N)2 et cycliques (N N)3, composés peu étudiés, pour des applications dans le domaine de la propulsion spatiale. La forte toxicité des hydrazines, utilisées actuellement dans les systèmes à biergols stockables et menacées par la réglementation REACH, impose aux industriels de les remplacer par de nouveaux ergols verts, aussi voire plus performants au niveau de la propulsion, mais surtout ne présentant aucun impact significatif sur la santé humaine et l’environnement. À ce jour, aucun candidat n’a été identifié pour remplacer
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Horner, Katherine A. "Synthesis and applications of triazole- and triazine-containing amino acids." Thesis, University of Leeds, 2015. http://etheses.whiterose.ac.uk/11024/.

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Through their use as mimics of post-translational modifications (PTMs) and in bioorthogonal chemical reporting strategies, unnatural amino acids (UAAs) are vital tools for studying biological systems. τ-Phosphotriazolylalanine I can act as a non-hydrolysable analogue of phosphohistidine and is compatible with the Fmoc-strategy for peptide synthesis. Peptides containing either I or an alternative phosphoamino acid were synthesised and used to demonstrate the selectivity of the SH2 domain of the growth factor receptor-bound 2 protein (a phosphotyrosine binding protein) towards τ-phosphohistidine
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Santos, Júlia Scherer. "Desenvolvimento de formulações fotoprotetoras contendo filtros solares nanoencapsulados." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2014. http://hdl.handle.net/10183/115970.

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A utilização de nanopartículas poliméricas como carreadores de filtros solares tem sido descrita na literatura, com intuito de possibilitar uma maior retenção desses no estrato córneo. Esse trabalho teve por objetivo desenvolver formulações nanotecnológicas fotoprotetoras a partir de variações na composição do núcleo oleoso e na composição quali-quantitativa dos filtros solares selecionados. Inicialmente, foram preparadas formulações contendo somente metoxicinamato de octila (OMC), afim de determinar a melhor concentração do filtro no núcleo. A análise da estabilidade dessas nanocápsulas mostr
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Khaldi, Zineb. "Elaboration et évaluation biologique de nouveaux matériaux lignocellulosiques antibactériens." Thesis, Limoges, 2018. http://www.theses.fr/2018LIMO0090/document.

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La contamination des surfaces par des bactéries et l’émergence de souches résistantes aux antimicrobiens sont des problèmes très préoccupants dans différents domaines tel que les domaines hospitalier et alimentaire. Cette contamination commence par l’adhésion de bactéries pathogènes sur une surface jusqu’à la formation de biofilms. Ces derniers contribuent à l’émergence de résistances de certaines souches bactériennes aux traitements conventionnels. Pour répondre à ces problèmes de contamination des surfaces, ces travaux de thèse portent sur le développement de nouveaux matériaux antibactérien
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Vieira, Andreia Sofia da Costa. "Rethinking Triazoles as Antifungals: Synthesis and Evaluation of New Triazole Derivatives." Master's thesis, Universidade Nova de Lisboa, Instituto de Tecnologia Química e Biológica António Xavier, 2017. http://hdl.handle.net/10362/81407.

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"In the last decades, fungal infections have become a serious problem, mainly due to the excessive use of this reduced number of drugs, leading to an increase of acquired resistances1. Therefore, it is urgent to develop new and more effective antifungal medicines. The main objective of this master's thesis was the development of novel antifungal drugs, based on triazoles and pyrimidines, combining two groups with antifungal properties, known to be active in combinatorial therapies, in a single molecule. For the synthesis of these compounds, Huisgen's 1,3-dipolar cycloaddition methodologies, c
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Litvinov, Dmitry Nikolayevich. "Celogentin C and Thioviridamide: Synthetic and Structural Studies." BYU ScholarsArchive, 2010. https://scholarsarchive.byu.edu/etd/2528.

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Project I Celogentin C, isolated by Kobayashi from the seeds of Celosia argentea in 2001 exhibits strong inhibitory behavior towards polymerization of tubulin – globular protein, which plays crucial role during the cell division cycle. We have attempted synthesis of the left-hand ring of celogentin C via the intramolecular alkylation and the Knoevenagel condensation strategies. Utilizing synthetic methodologies in the field of nitroacetyl chemistry, developed by Kornblum and Rajappa we have successfully prepared the intermolecular Knoevenagel condensation product – the late-stage precursor to
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Fiscus, David Michael. "The chemistry of 3-diazo-3H̲-1,4-triazole and 3H̲-1,2,4- triazol-3-ylidene /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487260135358319.

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Canduzini, Hugo Antonio. "Síntese e funcionalização de 1,2,3-triazóis via reação de cicloadição [3+2] de azidas e acetilenos terminais." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-07032013-094439/.

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O objetivo deste trabalho é explorar a síntese e funcionalização de 1,2,3- triazóis empregando o uso de reações do tipo \"Click-chemistry\", que é uma abordagem para a síntese de diversos compostos com base em reações de formação de ligação carbono-heteroátomo, onde a reação é estereoespecífica, altamente eficiente e geralmente com elevados rendimentos e em alguns casos ausência de subprodutos. O composto 1,2,3-triazol, sendo o material de partida para a continuidade do projeto foi preparado a partir do álcool propargílico (4) em presença de uma azida orgânica (1) e utilizando cobre(I) como ag
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Windisch, Alana Carolina. "Síntese de cristais líquidos discóticos derivados do núcleo trifenol tris-[1,2,4]-triazolo-[1,3,5]-triazina." reponame:Repositório Institucional da UFSC, 2014. https://repositorio.ufsc.br/xmlui/handle/123456789/131006.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas, Programa de Pós-Graduação em Química, Florianópolis, 2014.<br>Made available in DSpace on 2015-03-18T21:08:17Z (GMT). No. of bitstreams: 1 332778.pdf: 3083604 bytes, checksum: 5820bd0bf3c0d1e606e1add372e58ced (MD5) Previous issue date: 2014<br>Neste trabalho é descrito o planejamento, síntese e caracterização, além de estudos térmicos e ópticos de uma nova série de moléculas com estrutura discótica, facilmente sintetizadas a partir do versátil núcleo trifenol tristriazolotriazina. Todos
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Books on the topic "Triazone"

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Giraldi, Tullio, Thomas A. Connors, and Giuseppe Cartei, eds. Triazenes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3832-5.

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Ballantine, Larry G., Janis E. McFarland, and Dennis S. Hackett, eds. Triazine Herbicides: Risk Assessment. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0683.

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Košmrlj, Janez, ed. Click Triazoles. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29429-7.

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Dehaen, Wim, and Vasiliy A. Bakulev, eds. Chemistry of 1,2,3-triazoles. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-07962-2.

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Saka, John Danwell Kalenga. Studies in 1, 2, 3-triazine chemistry. University of East Anglia, 1985.

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Blackman, Claire. Studies on carbinolamine-containing triazine antitumour agents. University of Portsmouth, 1994.

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Patel, Ramesh. Triazines: Synthesis, applications, and toxicity. Nova Science Publishers, 2011.

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International, Conference on Trazenes: Chemical Biological and Clinical Aspects (1989 Trieste Italy). Triazenes: Chemical, biological, and clinical aspects. Plenum Press, 1990.

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United States. Environmental Protection Agency. Office of Pesticide Programs. Special Review and Reregistration Division. Reregistration eligibility decision: 1,3,5-triethylhexahydro-s-triazine, list C, case 3147. Environmental Protection Agency, Office of Pesticide Programs, Special Review and Reregistration Division, 1997.

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Byrne, John Joseph. Disease Control and Yield Improvement in Winter Wheat using Strobilurin and Triazole Chemistry. University College Dublin, 1998.

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Book chapters on the topic "Triazone"

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Bährle-Rapp, Marina. "Ethylhexyl Triazone." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3767.

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Bährle-Rapp, Marina. "Diethylhexyl Butamido Triazone." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2940.

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Aizpurua, Jesus M., Maialen Sagartzazu-Aizpurua, and Zaira Monasterio. "Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/7081_2014_120.

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Gooch, Jan W. "Triazine." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12076.

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Crowley, James D., and David A. McMorran. "“Click-Triazole” Coordination Chemistry: Exploiting 1,4-Disubstituted-1,2,3-Triazoles as Ligands." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2011_67.

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Wilman, Derry E. V. "Triazenes and Triazene N-Oxides: Antitumour Action in Animal Tumour Systems." In Triazenes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3832-5_3.

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Muir, D. C. G. "Triazine Herbicides." In Mass Spectrometry in Environmental Sciences. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2361-7_19.

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Edmunds, Andrew J. F. "Triazine Herbicides." In Bioactive Heterocyclic Compound Classes. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664412.ch2.

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Gooch, Jan W. "Trihydrazide Triazine." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12127.

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Gooch, Jan W. "Triazine Resin." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12077.

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Conference papers on the topic "Triazone"

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Jenkins, Alyn, Santosh Gopi, Jody Hoshowski, Warinthon Lertpornsuksawat, Jennifer Jackson, and Thomas Wilson. "Application of a New H2S Scavenger with Improved Performance in The Field." In SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206057-ms.

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The presence of hydrogen sulfide (H2S) gas occurs naturally, or can be introduced via bacteria contamination, in oil and gas reservoirs worldwide. There are several options for the removal of H2S from produced oil and gas ranging from fixed assets that scrub H2S to chemical injection at the wellsite. The area of interest for many operators is in the continuous application of non-reversible chemical H2S scavengers as an easy, reliable and cost-effective solution. The majority of the non-reversible chemical H2S scavenger market is based on triazine technology derived from the reaction products o
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Seijas, Julio A., M. Pilar Vázquez-Tato, María García-Fernández, Alberto Díaz-Seivane, and Xesús Feás. "Synthesis of 1H-1,2,3-Triazoles from Alkyne Derivatives of 1,3,5-Triazines by Huisgen\'s Reaction." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01097.

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Dolzhenko, Anton, Anna Dolzhenko, and Wai-Keung Chui. "Synthesis of 2,5,7-triamino[1,2,4]triazolo[1,5-a][1,3,5]triazines as potential antifolate agents." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01424.

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Dreyer, Christian, Alfred Blume, Monika Bauer, Jörg Bauer, and Jens Neumann-Rodekirch. "Triazine based Dendrimers." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01879.

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Chachibaia, Tamar, and Joy Hoskeri. "In silico computer simulation risk assessment of triazole fungicides on human cytochrome p450 aromatase enzyme: cyp19a1 inhibition by triazoles using autodock software." In MOL2NET, International Conference on Multidisciplinary Sciences. MDPI, 2015. http://dx.doi.org/10.3390/mol2net-1-f002.

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Silva, Marina Goulart da, Graziele Diniz da Silva, Clebson L.Veber, Andersson Barison, Gustavo H. R. Viana, and José Augusto F. P. Villar. "Design and synthesis of triazole-chalcones." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0263-1.

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Yu, Pan, Ningning Liu, Weiyuan Yuan, Yining Wen, and Qinpei Wu. "Synthesis of 1,2,3- Triazole Nucleoside Analogues." In 2015 International Conference on Industrial Technology and Management Science. Atlantis Press, 2015. http://dx.doi.org/10.2991/itms-15.2015.264.

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Alvarez, Jimmy, Christopher J. Bish, and Andres Rodriguez. "Introducing an Innovative Perfluoroelastomer Cross Linking Technology: Achieving Superior Chemical Resistance and Thermal Stability." In Offshore Technology Conference. OTC, 2021. http://dx.doi.org/10.4043/31229-ms.

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Objectives/Scope Perfluoroelastomers are a class of synthetic elastomers that provide extraordinary resistance to oils, chemicals, and heat. The outstanding thermal stability and excellent corrosion resistance of these materials is dependent on the perfluorinated polymer chain, and the absence of unsaturation. However, the cross-link which is necessary to impart elastomeric properties must also share those stability traits. Unfortunately, designing a suitably inert cross-link is technically difficult to achieve and consequently it has not been possible to provide the ultimate in perfluoroelast
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T. Supuran, Claudiu, Mohammed Arifuddin, Krishna kartheek, and Andrea Angeli. "Design, synthesis, and biological evaluation of 1,2,3-triazole-linked triazino[5,6-b]indole-benzene sulfonamide conjugates as potent carbonic anhydrase I, II, IX , and XIII inhibitors." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07395.

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Taylor, G. N., J. J. Wylde, T. Müller, J. Murison, and F. Schneider. "Fresh Insight into the H2S Scavenging Mechanism of MEA-Triazine vs. MMA-Triazine." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/184529-ms.

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Reports on the topic "Triazone"

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Xu, Y. E., and C. S. Sung. Photophysics of Polycyanate Resin and Triazine Compounds. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada327097.

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Kinkead, E. R., S. K. Bunger, and R. E. Wolfe. Irritation and Sensitization Studies on Triazine T17-2. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada221922.

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Caflin, Kelley C., and Peggy Sanchez. Solubility Report of 1-Methyl-3,5-Dinitro-1H-1,2,4-Triazole (MDNT) and 2-Methyl-4,5-Dinitro-2H-1,2,3-Triazole 1-Oxide (MDNTO) for Co-Crystallization Screen. Defense Technical Information Center, 2015. http://dx.doi.org/10.21236/ada627559.

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Tesfaselassie, Elias. Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2503.

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Cao, Cheng J., Gunda Reddy, Desmond I. Bannon, and Mark S. Johnson. In Vitro Study of Hexahydro-1,3,5-Trinitro-1,3,5-Triazine (RDX) Metabolism in Human Liver. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada638277.

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Haley, Mark V., Roman G. Kuperman, and Ronald T. Checkai. Aquatic Toxicity of 3-Nitro-1,2,4-Triazol-5-One. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada508035.

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Stromer, Bobbi, Rebecca Crouch, Katrinka Wayne, Ashley Kimble, Jared Smith, and Anthony Bednar. Methods for simultaneous determination of 29 legacy and insensitive munition (IM) constituents in aqueous, soil-sediment, and tissue matrices by high-performance liquid chromatography (HPLC). Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/1168142105.

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Standard methods are in place for analysis of 17 legacy munitions compounds and one surrogate in water and soil matrices; however, several insensitive munition (IM) and degradation products are not part of these analytical procedures. This lack could lead to inaccurate determinations of munitions in environmental samples by either not measuring for IM compounds or using methods not designed for IM and other legacy compounds. This work seeks to continue expanding the list of target analytes currently included in the US Environmental Protection Agency (EPA) Method 8330B. This technical report pr
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Adams, Valerie H. In Vitro Endocrine Disruption Screening of 3-nitro-1,2,4-triazol-5-one (NTO). Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ad1007533.

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Becher, Julie, Samuel Beal, Susan Taylor, Katerina Dontsova, and Dean Wilcox. Photo-transformation of aqueous nitroguanidine and 3-nitro-1,2,4-triazol-5-one : emerging munitions compounds. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41743.

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Two major components of insensitive munition formulations, nitroguanidine (NQ) and 3-nitro-1,2,4-triazol-5-one (NTO), are highly water soluble and therefore likely to photo-transform while in solution in the environment. The ecotoxicities of NQ and NTO solutions are known to increase with UV exposure, but a detailed accounting of aqueous degradation rates, products, and pathways under different exposure wavelengths is currently lacking. We irradiated aqueous solutions of NQ and NTO over a 32-h period at three ultraviolet wavelengths and analyzed their degradation rates and transformation produ
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Crouse, Lee C., and Arthur J. O'Neill. Acute Inhalation Toxicity and Blood Absorption of 3-Nitro-1,2,4-Triazol-5-One (NTO) in Rats. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada590390.

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