Relevant bibliographies by topics / 4-triazine

Contents

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

Academic literature on the topic '4-triazine'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "4-triazine"

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Fuerst, E. Patrick, Michael Barrett, and Donald Penner. "Control of Triazine-Resistant Common Lambsquarters (Chenopodium album) and Two Pigweed Species (Amaranthusspp.) in Corn (Zea mays)." Weed Science 34, no. 3 (1986): 440–43. http://dx.doi.org/10.1017/s0043174500067151.

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Various chemical treatments were evaluated over two growing seasons for control of triazine-resistant common lambsquarters (Chenopodium albumL. # CHEAL) and for control of a triazine-resistant infestation containing both redroot pigweed (Amaranthus retroflexusL. # AMARE) and Powell amaranth (A. powelliiS. Wats. # AMAPO). Atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine], cyanazine {2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl] amino]-2-methylpropanenitrile}, and metribuzin [4-amino-6-(1,1-dimethylethyl)-3-(methylthio)-1,2,4-triazin-5(4H)-one] provided unsatisfactory c
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Fuerst, E. Patrick, Charles J. Arntzen, Klaus Pfister, and Donald Penner. "Herbicide Cross-Resistance in Triazine-Resistant Biotypes of Four Species." Weed Science 34, no. 3 (1986): 344–53. http://dx.doi.org/10.1017/s0043174500066960.

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The cross-resistance of triazine-resistant biotypes of smooth pigweed (Amaranthus hybridusL. # AMACH), common lambsquarters (Chenopodium albumL. # CHEAL), common groundsel (Senecio vulgarisL. # SENVU), and the crop canola (Brassica napusL. var. Atratower) to a selection of herbicides was evaluated at both the whole plant and chloroplast level. The triazine-resistant biotypes of all four species showed a similar pattern of cross-resistance, suggesting that a similar mutation had occurred in each species. The four triazine-resistant biotypes were resistant to injury from atrazine [6-chloro-N-eth
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Deohate, Pradip P., and Roshani S. Mulani. "Microwave Irradiative Synthesis of Triazine Substituted Pyrazoles and Study of Antitubercular and Antimicrobial Activities." Asian Journal of Chemistry 31, no. 5 (2019): 1087–90. http://dx.doi.org/10.14233/ajchem.2019.21826.

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Microwave irradiative synthesis of triazine substituted pyrazoles i.e. (4-benzylideneamino-6-methyl-[1,3,5]-triazin-2-yl)-(5-methyl-2-substituted benzoyl/isonicotinoyl/cinnamoyl-pyrazol-3-yl)-amines have been achieved by the cyclocondensation of N-(4-benzylideneamino-6-methyl-[1,3,5]-triazin-2-yl)-3-oxo butyramide with substituted acid hydrazides. Synthesis of required butyramide was done by reacting 2,4-diamino-6-methyl-[1,3,5]-triazine with benzaldehyde and then condensing the product with ethyl acetoacetate. Structural investigation of synthesized compounds has been done by chemical transfo
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GAYNOR, J. D., J. A. STONE, and T. J. VYN. "TILLAGE SYSTEMS AND ATRAZINE AND ALACHLOR RESIDUES ON A POORLY DRAINED SOIL." Canadian Journal of Soil Science 67, no. 4 (1987): 959–63. http://dx.doi.org/10.4141/cjss87-091.

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Seasonal residues of an acetanilide and triazine herbicide were monitored in ridge, conventional, and zero tillage systems. Alachlor (2-chloro-2′,6′-diethyl-N-(methoxymethyl)acetanilide), and atrazine (2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine) residues were less than 8% of the spring application concentration at the end of the growing season. Moldboard plowing in the fall reduced herbicide residues in spring because of soil dilution by plowing to greater than the sampling depth. Ridge tillage systems had higher spring residues apparently because of reduced herbicide dissipation on
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Chaudhari, J. A., R. P. Patel, and M. V. Hathi. "Studies on Novel Bisaryl Hydrazino-s-triazine Derivatives - Part 2." E-Journal of Chemistry 4, no. 3 (2007): 385–89. http://dx.doi.org/10.1155/2007/805637.

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Various 2(4-chloro phenyloxy)-4,6-bisarylhydrazino-1,3,5-triazines(3a-f) were prepared by reaction of 2(4-chloro phenyloxy)-4,6-dichloro -1,3,5-triazine and various aryl hydrazine derivatives. All the 3a-f derivatives were characterized by elemental analysis and IR spectral studies. All the compounds were screened for microbial activity against gram-positive and gram-negative bacteria.
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Collins, David J., Timothy C. Hughes, and Wynona M. Johnson. "Dihydro-1,2,4-triazin-6(1H)-ones. III. Oxidation Products of 1-Methyl-3-phenyl- 4,5-dihydro-1,2,4-triazin-6(1H)-one." Australian Journal of Chemistry 52, no. 10 (1999): 971. http://dx.doi.org/10.1071/ch99047.

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1-Methyl-3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one (1) undergoes aerial oxidation to give a mixture of 1- methyl-3-phenyl-1,2,4-triazin-6(1H)-one (2) and 1-methyl-3-phenyl-1,4-dihydro-1,2,4-triazine-5,6-dione (3). The dehydro derivative (2) was cleanly prepared by the oxidation of (1) with 2,3-dichloro-5,6-dicyano-1,4- benzoquinone (ddq). The dehydro derivative (2) underwent a surprising rearrangement to the triazole (12) upon oxidation with OxoneR. Several attempts at unambiguous synthesis of the α-dicarbonyl derivative (3) were unsuccessful; it was obtained, together with the 1,4-dimethyl
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Kumar, Vipan, Manish Gupta, and M. P. Mahajan. "Effect of the nature of substituents on aromatic aldehydes in microwave induced N-cyclohexylamidine–aldehyde condensation reactions." Canadian Journal of Chemistry 84, no. 3 (2006): 453–57. http://dx.doi.org/10.1139/v06-014.

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A simple, environmentally friendly protocol for the selective synthesis of the 4-aryl substituted acyclic 1,3-dienes and the medicinally potent triazines has been developed using a domestic microwave oven with excellent yields and reproducibility.Key words: microwave, dihydrotriazine, triazine, imine metathesis.
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Jeon, Youngeun, Jineun Kim, Gihang Kang, and Tae Ho Kim. "Crystal structure of anilazine." Acta Crystallographica Section E Structure Reports Online 70, no. 9 (2014): o923. http://dx.doi.org/10.1107/s160053681401647x.

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The title compound [systematic name: 4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazin-2-amine], C9H5Cl3N4, is a triazine fungicide. The dihedral angle between the planes of the triazine and benzene rings is 4.04 (8)°. In the crystal, two weak C—H...N hydrogen bonds and short Cl...Cl contacts [3.4222 (4) Å] link adjacent molecules, forming two-dimensional networks parellel to the (112) plane. The planes are linked by weak intermolecular π–π interactions [3.6428 (5) and 3.6490 (5) Å], resulting in a three-dimensional architecture.
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Braun, Dietrich, Reza Ghahary, and Harald Pasch. "Triazine-based polymers: 4. MALDI-MS of triazine-based polyamines." Polymer 37, no. 5 (1996): 777–83. http://dx.doi.org/10.1016/0032-3861(96)87253-3.

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Kunishima, Munetaka, Daiki Kato, Nobu Kimura, Masanori Kitamura, Kohei Yamada, and Kazuhito Hioki. "Potent triazine-based dehydrocondensing reagents substituted by an amido group." Beilstein Journal of Organic Chemistry 12 (August 24, 2016): 1897–903. http://dx.doi.org/10.3762/bjoc.12.179.

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This study describes the synthesis of triazine-based dehydrocondensing reagents substituted by amido substituents and demonstrates their efficiency for dehydrocondensing reactions in MeOH and THF. N-Phenylbenzamido-substituted chlorotriazine is readily converted to a stable, non-hygroscopic triazinylammonium-based dehydrocondensing reagent that is superior to 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) in terms of its reactivity in dehydrocondensing reactions.
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Dissertations / Theses on the topic "4-triazine"

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Dupont, Carine. "Conception, synthèse et caractérisation de molécules polyhétérocycliques azotées pour la complexation spécifique de cations métalliques." Phd thesis, Université d'Orléans, 2010. http://tel.archives-ouvertes.fr/tel-00590462.

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La loi du 6 juin 2006 sur la gestion des déchets radioactifs de haute activité et à vie longue prévoit la recherche de solutions permettant la séparation et la transmutation des radioéléments à vie longue, pour réduire les quantités et la nocivité des déchets radioactifs ultimes. Ces déchets issus du retraitement du combustible nucléaire usé sont actuellement vitrifiés à La Hague. Ainsi, le projet " séparation poussée " vise à compléter le procédé industriel PUREX par le développement de procédés permettant d'extraire les actinides mineurs des raffinats PUREX où se trouvent également des produ
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Le, Falher Laetitia. "Préparation et dérivatisation de 4H-pyrido[e][1,3]oxazinones : une contribution à la diversité chimique." Thesis, Paris 6, 2014. http://www.theses.fr/2014PA066344.

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Ce manuscrit porte sur la synthèse et les applications d'une nouvelle série de composés hétéroaromatiques : les 4H-pyrido[e][1,3]oxazin-4-ones. La première partie de ce manuscrit présente la préparation de ces squelettes via une réaction d'O-arylation intramoléculaire. La seconde partie du manuscrit repose sur la réactivité de ces entités chimiques et de leur utilisation en tant qu'intermédiaires de synthèse. La fonctionnalisation des 4H-pyrido[e][1,3]oxazin-4-ones, via des réactions de couplage pallado-catalysées, a permis d'obtenir des systèmes polyfonctionnalisés plus complexes. Les pyrido-
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Badarau, Eduard. "Conception, synthèse et évaluation biologique de nouvelles classes de ligands sérotoninergiques 5-HT7." Phd thesis, Université d'Orléans, 2009. http://tel.archives-ouvertes.fr/tel-00480279.

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Parmi tous les neurotransmetteurs identifiés à ce jour, la sérotonine (5-hydroxytryptamine, 5-HT) est impliquée dans le système le plus complexe de récepteurs. Parmi eux, les récepteurs 5-HT7 qui sont les derniers découverts (1993) semblent avoir des implications multiples tant au niveau central que périphérique. Le potentiel thérapeutique représenté par la découverte de ligands 5-HT7 sélectifs vis-à-vis d'autres RCPGs a motivé notre projet de recherche. Nos études sont orientées vers la conception de trois classes distinctes de ligands. Une première famille à été conçue sur une charpente benz
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DU, MOULIN DE LA BRETECHE MARIE-LAURE. "Modification de composes aromatiques en conditions douces : bioconversion de la 2-chloro 4-ethylamino 6-isopropylamino 1,3,5-triazine ou atrazine ; etude de la nitrosation de phenols substitues et des catecholamines." Paris 11, 1994. http://www.theses.fr/1994PA112320.

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La chimie en conditions douces s'avere une alternative de choix, a la fois lors de l'etude de molecules sensibles aux conditions de ph et d'oxydo-reduction, et lors de l'etude des processus physiologiques. L'illustration de ces methodes a ete realisee dans le cas de la biodegradation de l'atrazine, herbicide qui s'accumule dans les sols et dans l'eau et de la reactivite des nitrites sur les phenols. La bioconversion de l'atrazine a ete effectuee par des microorganismes issus du milieu naturel. Les champignons filamenteux rhizopus arrhizus, curvularia lunata et beauveria bassiana transforment l
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Woodland, Elaine Denise. "Investigations of fused 1,2,3-triazin-4-ones and related systems." Thesis, Nottingham Trent University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304105.

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This thesis describes work carried out on several chemical aspects of fused 1,2,3-triazin-4-ones. In the first section several sUbstituted l,2,3-benzotriazinones were prepared with a view to observing their rate of deazoniation. It ,was envisaged that a kinetic analysis of this reaction would aid the elucidation of the nature of a hitherto controversial reaction intermediate. The rate constants obtained were used to construct Hammett plots and hence calculate the reaction constants. Several pieces of evidence were obtained that suggested the intermediate was of a diradical nature. Unfortunatel
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FIOROT, R. G. "Síntese e Estudo de Ancoragem Molecular de Novos Híbridos Contendo Os Núcleos 1,4-naftoquinônico, Quinolínico e 1,3,5-triazínico Com Potencial Atividade Antineoplásica." Universidade Federal do Espírito Santo, 2015. http://repositorio.ufes.br/handle/10/4744.

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Made available in DSpace on 2016-08-29T15:35:41Z (GMT). No. of bitstreams: 1 tese_9160_Rodolfo Goetze Fiorot.pdf: 12436359 bytes, checksum: f6d3dc79a76780f5d4d2ad8a84ce69cc (MD5) Previous issue date: 2015-09-04<br>O câncer é uma das doenças mais temidas pela sociedade, sendo uma das principais causas de morte em todo o mundo. Desta maneira, estudos contínuos buscando compreender seus mecanismos de evolução são imprescindíveis para que se possa erradica-lo do organismo. Embora a quimioterapia seja amplamente empregada em praticamente todos os casos de câncer, a resistência a múltiplas drogas
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Pochet, Sylvie. "Synthèse d'oligodésoxynucléotides comportant des sites ambigus ou apuriniques et de sondes ancrées à un support solide." Paris 6, 1986. http://www.theses.fr/1986PA066065.

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Synthèse et étude par spectroscopies RMN, IR et DC d'oligodésoxyribonucléotides contenant un résidu sans base: coexistence des conformations b et z sur un même duplex. Elaboration d'une base universelle dans la série des nucléosides pyrimidiques. Synthèse d'oligodésoxynucléotides ancrés à un support solide; applications.
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Edmont, Blotière Dolores. "Synthèse et réactivité de la 6-fluoro-4-oxo-1, 4-dihydro-2-quinoléinecarboxylate de méthyle : Elaboration de novuelles molécules tricycliques à structure 1,2,4-triazino. Evaluation biologique dans le domaine hypoglycémiant." Orléans, 1999. http://www.theses.fr/1999ORLE2009.

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Le diabete mellitus, maladie metabolique, est un syndrome de plus en plus frequent, qui se rencontre a tous les ages de la vie. Des donnees recentes revelent l'existence d'environ 130 millions de diabetiques dans le monde et leur nombre pourrait bien doubler d'ici 2025. Dans le cadre d'une recherche de nouveaux agents hypoglycemiants permettant de traiter les causes et les consequences du diabete non insulino-dependant, nous avons prepare, a partir d'un synthon de base de 6-fluoro-4-oxo-1,4-dihydro-2-quinoleinecarboxylate de methyle, des composes du type 4-oxo-1,4-dihydroquinoleinique diversem
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Leconte, Nicolas. "Synthèse et caractérisation de molécules polyhétérocycliques azotées pour la complexation de cations metalliques polluants." Phd thesis, Université d'Orléans, 2007. http://tel.archives-ouvertes.fr/tel-00465122.

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La séparation des actinides(III) du mélange actinides(III)/lanthanides(III) constitue un problème crucial dans le retraitement du combustible nucléaire usé. Il a été montré expérimentalement que les dérivés de la 2,6-bis(1,2,4-triazin-3-yl)pyridine (BTP) sont capables d'extraire sélectivement les actinides(III) par rapport aux lanthanides(III). Cependant, les propriétés de ces molécules doivent être améliorées pour afficher de meilleures performances d'extraction et pour résister aux conditions dures du milieu à extraire. Des ligands fonctionnalisés de manière originale ont été synthétisés pui
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Hajbi, Youssef. "Application de la réaction de Diels-Alder à demande électronique inverse à la synthèse de nouveaux composés oxygénés et azotés à visée thérapeutique." Phd thesis, Université d'Orléans, 2007. http://tel.archives-ouvertes.fr/tel-00151105.

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Cette thèse s'inscrit dans une volonté de développer de nouvelles architectures hétéroaromatiques susceptible de montrer un potentiel thérapeutique. Pour cela la synthèse de dihydrofuro[2,3-b]pyridines et dihydropyrano[2,3-b]pyridines hautement et diversement fonctionnalisées est apparue particulièrement intéressante notamment en vue de l'obtention de nouveaux analogues sérotoninergiques. L'accès à ces nouveaux squelettes a été réalisé via une réaction intramoléculaire de Diels-Alder à demande électronique inverse avec des 1,2,4-triazines. <br /><br />Pour ce faire, des 3-méthylsulfanyl-1,2,4-
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Books on the topic "4-triazine"

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Neunhoeffer, Hans, and Paul F. Wiley. Chemistry of 1 2 3-Triazines and 1 2 4-Triazines, Tetrazines, and Pentazin. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "4-triazine"

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "2,4-Bis(octylmercapto)-6-(4-hydroxy-3,5-di-tert-butylanilino)-1,3,5-triazine." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_17.

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-1,3,5-triazine-2,4,6(1H,3H,5H)trione." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_102.

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "Poly[6-[(1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)-imino]hexamethylene[(2,2,6,6-tetramethyl-4-piperidyl)imino]." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_82.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 3-hydrazino-5, 6-diphenyl-1, 2, 4-triazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_175.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with 3-hydrazino-5, 6-diphenyl-1, 2, 4-triazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_347.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of chromium(III) complex with 3-hydrazino-5, 6-diphenyl-1, 2, 4-triazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_458.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with 3-hydrazino-5, 6-diphenyl-1, 2, 4-triazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_635.

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Lindsley, C. W., and M. E. Layton. "C3-Amination of 1,2,4-Triazine 4-Oxides." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00637.

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Aggarwal, P., and M. W. P. Bebbington. "Reaction of 1,2,4-Triazine 4-Oxides with Terminal Alkynes." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00260.

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Aggarwal, P., and M. W. P. Bebbington. "Nucleophilic Addition of Cyanide to 1,2,4-Triazine 4-Oxides." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00269.

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Conference papers on the topic "4-triazine"

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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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Anichina, K. "SYNTHESIS AND ANTINEMATODAL ACTIVITY STUDIES OF SOME FUSED TRIAZINOBENZIMIDAZOLES." In International Trends in Science and Technology. RS Global Sp. z O.O., 2020. http://dx.doi.org/10.31435/rsglobal_conf/30122020/7351.

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4-Aryl-3,4-dihydro[1,3,5]triazino[1,2-a]benzimidazole-2-amines 3a-f were synthesized in the reaction of cyclocondensation between 2-guanidinobenzimidazole and versatilebenzaldehydes. Structures of all prepared compounds were confirmed by IR, 1H NMR spectroscopyand elemental analysis.Antinematodal activity in vitro of the substances was investigated using isolated Trichinella spiralis muscle larvae. The tested triazonobenzimidazoles showed different activity depending on the substituent R in their moleculeas the derivatives substituted with a hydroxyl group demonstrated the best anti-Trichinell
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Jin, Meizhong, Prafulla Gokhale, Andy Cooke, et al. "Abstract 3900: Discovery of FQIT: An imidazo[5,1-f][1,2,4]triazine derived dual IGF-1R/IR inhibitor." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3900.

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Dolzhenko, Anton, Anna Dolzhenko, and Wai-Keung Chui. "Synthesis of Fused 2-amino-4-oxo-1,3,5-triazines via Microwave-Assisted Ring Closure Carbonylation of Azahetarylguanidines." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01635.

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Dolzhenko, Anton, Anna Dolzhenko, and Wai-Keung Chui. "Reaction of 2-amino-4-aryl-3,4-dihydro[1,3,5]triazino[1,2-a]-benzimidazoles with diethyl ethoxymethylenemalonate." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01381.

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Xiang, Haoyue, Xiang Wang, Yanhong Chen, et al. "Abstract LB-268: Discovery of clinical candidate methyl (5-(6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinopyrrolo[2,1-f][1,2,4]triazin-2-yl)-4-(trifluoromethyl)pyridin-2-yl)carbamate (CYH33) : A highly potent and selective PI3K alpha inhibitor for the treatment of advanced solid tumors." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-lb-268.

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Reports on the topic "4-triazine"

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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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Abstract:
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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