Relevant bibliographies by topics / Naphthalenone

Contents

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

Academic literature on the topic 'Naphthalenone'

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

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Journal articles on the topic "Naphthalenone"

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Ibrahim, Sabrin R. M., Sana A. Fadil, Haifa A. Fadil, Bayan A. Eshmawi, Shaimaa G. A. Mohamed, and Gamal A. Mohamed. "Fungal Naphthalenones; Promising Metabolites for Drug Discovery: Structures, Biosynthesis, Sources, and Pharmacological Potential." Toxins 14, no. 2 (2022): 154. http://dx.doi.org/10.3390/toxins14020154.

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Fungi are well-known for their abundant supply of metabolites with unrivaled structure and promising bioactivities. Naphthalenones are among these fungal metabolites, that are biosynthesized through the 1,8-dihydroxy-naphthalene polyketide pathway. They revealed a wide spectrum of bioactivities, including phytotoxic, neuro-protective, cytotoxic, antiviral, nematocidal, antimycobacterial, antimalarial, antimicrobial, and anti-inflammatory. The current review emphasizes the reported naphthalenone derivatives produced by various fungal species, including their sources, structures, biosynthesis, a
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Paat, F. J., S. Wantasen, M. M. Toding, et al. "GC-MS method for identification of organic chemical compounds nutmeg flesh of North Minahasa local varieties." IOP Conference Series: Earth and Environmental Science 1241, no. 1 (2023): 012004. http://dx.doi.org/10.1088/1755-1315/1241/1/012004.

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Abstract The organic chemical compound Myristica fragrans has been identified in North Minahasa Regency. This study succeeded in identifying Neoisolongifolane, hydroxy-, 1HCyclopropa [a]naphthalene, 1a, 2, 3, 5, 6, 7, 7a, 7b-octahydro-1, 1, 7, 7a-tetramethyl, [1aR(1aα,7a,7aα,7bα)]-; 4,7-Methanoazulene, 1, 2, 3, 4, 5, 6, 7, 8-octahydro-1, 4, 9, 9-tetramethyl-, [1S-(1a,4a,7a)]-; Patchouli alcohol, 1(2H)- Naphthalenone, octahydro-4a, 8a-dimethyl-7-(1-ethylethyl)- [4aR-(4aα,7ß,8aα)]-, and Isoleden.
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Song, Xiaohan, Xu Han, Rui Zhang, Hong Liu, and Jiang Wang. "Rhodium(III)-Catalyzed [4+2] Annulation via C-H Activation: Synthesis of Multi-Substituted Naphthalenone Sulfoxonium Ylides." Molecules 24, no. 10 (2019): 1884. http://dx.doi.org/10.3390/molecules24101884.

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A convenient Rh(III)-catalyzed C-H activation and cascade [4+2] annulation for the synthesis of naphthalenone sulfoxonium ylides has been developed. This method features perfect regioselectivity, mild and redox-neutral reaction conditions, and broad substrate tolerance with good to excellent yields. Preliminary mechanistic experiments were conducted and a plausible reaction mechanism was proposed. The new type naphthalenone sulfoxonium ylides could be further transformed into multi-substituted naphthols, which demonstrates the practical utility of this methodology.
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Joshi Shrestha, Sudha. "Volatile organic metabolites and their importance in Senecio L. (Senecioneae: Asteraceae)." Botanica Orientalis: Journal of Plant Science 10 (November 1, 2016): 12–18. http://dx.doi.org/10.3126/botor.v10i0.21018.

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The present work aims to characterize volatile secondary metabolites in Senecio L. for delimiting taxa at the infrageneric level. Analysis of n-hexane fraction of ethanolic extracts of five species of Senecio L. (S. laetus Edgew., S. nudicaulis Buch.-Ham. ex D. Don, S. raphanifolius Wall. ex DC., S. royleanus DC. and S. scandens Buch.-Ham. ex D. Don) from Nepal Himalaya revealed the presence of a number of volatile secondary metabolites. Among them, 17 metabolites, viz., acorenol, bergamotene, cadin, cadinene, calarene, caryophyllene, cumialdehyde, cycloprop(e)azulene, elemol, farnesene, hexan
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Cheng, Peiming, Lixuan Cai, Danni Yan, Lipeng Zhou, and Qingfu Sun. "Molecular Cage Promoted Aerobic Oxidation or Photo-Induced Rearrangement of Spiroepoxy Naphthalenone." Catalysts 11, no. 4 (2021): 484. http://dx.doi.org/10.3390/catal11040484.

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Herein, we report a Pd4L2-type molecular cage (1) and catalyzed reactions of spiroepoxy naphthalenone (2) in water, where selective formation of 2-(hydroxymethyl)naphthalene-1,4-dione (3) via aerobic oxidation, or 1-hydroxy-2-naphthaldehyde (4) via photo-induced rearrangement under N2 have been accomplished. Encapsulation of four molecules of guest 2 within cage 1, i.e., (2)4⊂1, has been confirmed by NMR, and a final host-guest complex of 3⊂1 has also been determined by single crystal X-Ray diffraction study. While the photo-induced ring-opening isomerization from 2 to 4 are known, appearance
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Ning, Yaoyao, Xiaoqing Wang, Kangjia Sheng, et al. "A novel colorimetric and fluorescence turn-on pH sensor with a notably large Stokes shift for its application." New Journal of Chemistry 42, no. 17 (2018): 14510–16. http://dx.doi.org/10.1039/c8nj02860e.

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Shan, R., M. Stadler, H. Anke, and O. Sterner. "Naphthalenone and Phthalide Metabolites fromLachnum papyraceum1." Journal of Natural Products 60, no. 8 (1997): 804–5. http://dx.doi.org/10.1021/np970145s.

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Li, Jian, Haibo Huo, Fang Yang, et al. "Gold(iii)-catalyzed bicyclizations of alkylidenecyclopropane-tethered ynones for divergent synthesis of indene and naphthalenone-based polycycles." Organic Chemistry Frontiers 8, no. 17 (2021): 4853–59. http://dx.doi.org/10.1039/d1qo00821h.

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A gold(iii)-catalyzed cascade oxidation/cyclization of alkylidenecyclopropane-tethered ynones for the assembly of indene and naphthalenone-based polycycles by employing different N-oxides is reported.
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Fan, Yan-Hui, Xiao-Yu Guan, Wen-Pei Li та ін. "Synthesis of amidines via iron-catalyzed dearomative amination of β-naphthols with oxadiazolones". Organic Chemistry Frontiers 9, № 2 (2022): 380–85. http://dx.doi.org/10.1039/d1qo01687c.

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An efficient and convenient method for the synthesis of amidines bearing a β-naphthalenone moiety catalyzed by cheap iron(ii) chloride is presented by employing oxadiazolones as the nitrene precursors.
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Semar, Martin, Heidrun Anke, Wolf-Rüdiger Arendholz, Robert Veiten, and Wolfgang Steglich. "Lachnellins A, B, C, D, and Naphthalene-l,3,8-triol, Biologically Active Compounds from a Lachnellula Species (Ascomycetes)." Zeitschrift für Naturforschung C 51, no. 7-8 (1996): 500–512. http://dx.doi.org/10.1515/znc-1996-7-808.

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Abstract In the course of our search for new biologically active metabolites, lachnellin A (1), a metabolite with high cytotoxic and antimicrobial activities, the structurally related lachnellins B, C and D (3, 4, 7), and naphthalene-1,3,8-triol (8), an inhibitor of malate synthase (EC 4.1.3.2), were isolated from submerged cultures of the ascomycete Lachnellula sp. A 32 -8 9 . The antimicrobial, cytotoxic and phytotoxic activities of lachnellin A depended on its reactivity and could be abolished by the addition of cysteine. The enzyme inhibiting activity of (8) was due to reactive intermediat
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Dissertations / Theses on the topic "Naphthalenone"

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Quinn, Samuel. "Colouring naphthalene diimides." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50038/.

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Naphthalene diimides have been explored in a wide variety of ways; They are a promising candidate for organic electronics, boasting the ability to form n-type semiconductor materials, the stability of their anions further aiding in this regard. Their electron poor aromatic core can be used in host guest chemistry to generate interlocked species. The ability to tune their electronic properties and how this could be manipulated to create photovoltaic devices is primarily focus of this thesis. A series of naphthalene diimides substituted at the core with morpholine moieties have been synthesized
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Nehls, Benjamin S. "Naphthalene based conjugated materials." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=976731363.

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Kim, Michelle B. "The Hydrolysis of Naphthalene Diimides." Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/chemistry_theses/7.

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The hydrolyses of naphthalene diimides (NDIs) bearing aliphatic side chains with N-methylpyrrolidinium groups placed two (1) and three (5) atoms from the central core were studied. The Ka values for the first and second hydrolyses for 1 were 2.5 ± 0.2 x 105 M-1 and 2.0 ± 0.1 x 102 M-1, respectively; for 5 they were 1.4 ± 0.1 x 105 M-1 and 44 ± 2 M-1, respectively. NDI 1 hydrolyzed 6.8 times faster than did 5. The rates for the first and second hydrolyses of 1 at 100 mM hydroxide measured by stopped-flow were 17.0 ± 0.2 s-1 and 53.0 ± 0.1 x 10-2 s-1, respectively. NMR showed both the syn and an
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黃文菁 and Man-ching Wong. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzoneA." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B31211033.

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Wong, Man-ching. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzone A /." [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13457093.

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Gubellini, Federico. "Designing heterogeneous catalysts for naphthalene isopropylation." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/20659/.

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2,6 di-isopropylnaphthalene is a plant growth regulator and it is used for the manufacturing of products intended to prevent sprouting of stored potatoes; despite that in the last decades it has been mainly produced as a precursor of the corresponding dicarboxylic acid (2,6-naphthalene dicarboxylic acid) which is, with ethylene glycol, the monomer for polyethylene naphthalate (PEN) polymerization. PEN results appealing for many uses for which PET is more commonly utilized; the most relevant, higher glass transition temperature (PEN 122°C, PET 80°C), higher Young’s modulus (PEN 5200 MPa, PET 3
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Bakker, M. G. "ESR studies on some naphthalene derivatives." Thesis, University of Canterbury. Chemistry, 1985. http://hdl.handle.net/10092/8639.

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ESR Spectroscopy has been used to study conformational interconversion and addivity relationships in a number of series of naphthalene derivatives. Oscillation of the alkyl rings in 1,2,3,6,7,8-hexahydropyrene ions, and the ions of the related 5, 6 and 7 membered ring compounds has been studied. The temperature dependance of the ESR spectra have been used to assign the coupling constants. The aromatic ring coupling constants in the asymmetric compounds have been assigned on the basis of an additivity relationship. The ESR spectra of a number of methylnaphthalene anions have been recorded and
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Carey, Michelle Jocelyn. "The photophysics of naphthalene containing synthetic polymers." Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320273.

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Senior, Kerry Charles. "Biotreatment of industrial effluents containing naphthalene sulphonate." Thesis, University of Kent, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270819.

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LaPlante, Troy David. "Supercritical fluid extraction of naphthalene from soil slurries." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0003/MQ31844.pdf.

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Books on the topic "Naphthalenone"

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances Disease Registry, Division of Toxicology, Dept. of Health and Human Services, Public Health Service, 2005.

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naftalina, 1-metilnaftalina y 2-metilnaftalina. Agencia para Sustancias Tóxicas y el Registro de Enfermedades, División de la Toxicología, Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, 2005.

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Antsyforov, Gleb I., and Alyona F. Ivanski. Napthalene: Structure, properties, and applications. Nova Science Publishers, 2011.

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D, Nitterauer James, and United States. Environmental Protection Agency, eds. Biotransformation of benzothiophene by isopropylbenzene-degrading bacteria. Environmental Protection Agency], 1994.

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Nii͡azov, A. N. Naftenaty. Ylym, 1992.

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United States. Environmental Protection Agency. Emissions Standards and Engineering Division. and United States. Environmental Protection Agency. Office of Air Quality Planning and Standards., eds. Summary of emissions associated with sources of naphthalene. U.S. Environmental Protection Agency, 1986.

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Kreutz, Martin. Halogen-Metall-Austausch bei Bromnaphthalinen: Synthese, Struktur, und Reaktionsweisen mono- und polylithiierter Naphthaline. A.S. Intemann, 1991.

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Humans, IARC Working Group on the Evaluation of Carcinogenic Risks to. Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. IARC Press, 2002.

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Hisham, El-Masri, United States. Agency for Toxic Substances and Disease Registry., United States. Environmental Protection Agency., and Syracuse Research Corporation, eds. Toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances and Disease Registry, 2005.

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Derner, Harald. Untersuchungen über den Resonanz-Ramaneffekt an Anthracen, Naphthalin und p-nitro-p-dimethylamino-azobenzol. Hochschulverlag, 1986.

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Book chapters on the topic "Naphthalenone"

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Turhan, Munire. "Moisture, Electrical Conductivity, Water-Insoluble Solid Matter, Free Acidity and Ph Analysis Methods in Honey." In Methods of Biochemical Analysis of Bee Products. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359326.2.

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Honey is a very important natural food consumed as a source of healing. However, it can become harmful due to different chemicals mixed into the content of honey. Naphthalene is a carcinogenic hydrocarbon compound that forms residues in honey. Naphthalene, which beekeepers use to prevent honeycombs from mothballing but are prohibited from using, has many harmful effects on health. The Turkish Food Codex Honey Communiqué states that naphthalene in honey can be at a maximum concentration of 10 µm/kg. Many international organizations and states have set this limit. Therefore, naphthalene analysis
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Izol, Ebubekir. "Naphthalene Analysis in Honey by Gas Chromatography Technology." In Methods of Biochemical Analysis of Bee Products. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359326.1.

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Honey is a very important natural food consumed as a source of healing. However, it can become harmful due to different chemicals mixed into the content of honey. Naphthalene is a carcinogenic hydrocarbon compound that forms residues in honey. Naphthalene, which beekeepers use to prevent honeycombs from mothballing but are prohibited from using, has many harmful effects on health. The Turkish Food Codex Honey Communiqué states that naphthalene in honey can be at a maximum concentration of 10 µm/kg. Many international organizations and states have set this limit. Therefore, naphthalene analysis
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Capinera, John L., Marjorie A. Hoy, Paul W. Paré, et al. "Naphthalene." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_2142.

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Bailey, Lisa A., Laura E. Kerper, and Lorenz R. Rhomberg. "Naphthalene." In Hamilton & Hardy's Industrial Toxicology. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch65.

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Gooch, Jan W. "Naphthalene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7776.

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Lide, David R. "Naphthalene." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-358.

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Bährle-Rapp, Marina. "Dibenzoxazoyl Naphthalene." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2867.

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Schomburg, Dietmar, and Dörte Stephan. "Naphthalene 1,2-dioxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_81.

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Wohlfarth, Ch. "Viscosity of naphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_335.

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Vogt, J. "731 C10H8O 1-Naphthalenol." In Asymmetric Top Molecules. Part 3. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_153.

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Conference papers on the topic "Naphthalenone"

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Jia, Dan, Huimin Liu, and Dongyan Gu. "Preparation of Naphthalene Molecularly Imprinted Absorbent and its adsorption for Naphthalene." In 2017 3rd International Forum on Energy, Environment Science and Materials (IFEESM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/ifeesm-17.2018.288.

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Melker, Alexander I., Dimitri A. Kornilov, Tatiana V. Vorobyeva, and Denis Kalinin. "Conformational transitions in naphthalene." In SPIE Proceedings, edited by Alexander I. Melker. SPIE, 2004. http://dx.doi.org/10.1117/12.555442.

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Junbiao Peng, Runguang Son, Yuguang Ma, Haifeng Zhang, and Shiyong Liu. "Electroluminescent of plasma polymerized naphthalene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835421.

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Ciocci, Richard C. "Characterizing Naphthalene via Material Flow Analysis." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-82808.

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An Environmental Protection Agency-funded project centers on the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The analysis commences with manufacturers who use naphthalene-containing products in their processes. Also, the analysis works in reverse by starting with the naphthalene user, as the material will be traced to the source in an effort to identify elimination/reduction opportunities throughout the material’s life cycle. A particular focus is the potential for removal of naphthalene from the primary pr
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Ciocci, Richard, Daniel Massey, and Steve Funck. "Developing a Process to Identify Material Flow of a Priority Chemical." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-13727.

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An Environmental Protection Agency-funded project was the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The project analysis began with manufacturers who use naphthalene-containing products in their processes. It identifies the basic characteristics of naphthalene as a common polynuclear aromatic hydrocarbon, which is released to the environment. Included are likely sources of naphthalene emissions and releases as they were identified for further investigation. This paper, which is the sequel to IMECE 2005-82
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Nikulina, N., Sergey Nikulin, and A. Dmitrenkov. "PRODUCTION OF MODIFIED WOOD USING VINYL NAPHTHALENE DERIVATIVE." In ENERGY-SAVING AND ENVIRONMENTALLY SAFE TECHNOLOGIES OF THE TIMBER INDUSTRY – 2025. FSBE Institution of Higher Education Voronezh State University of Forestry and Technologies named after G.F. Morozov, 2025. https://doi.org/10.58168/e-sestti2025_284-288.

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The compositions for processing natural birch wood, obtained on the basis of ethenyl derivatives of naphthalene, are investigated in the work. A solution of naphthalene derivatives in toluene with additives of pinane hydroperoxide was used for wood processing. The removal of toluene from modified timber samples was combined with radical polymerization of ethenyl naphthalene derivatives in an autoclave at 160-165 0C for 5 hours. The polymer content in the timber varied from 10 to 26%. Manufactured timber products containing ethenyl naphthalene derivatives will provide products based on them not
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Song, Fu, Yifei Shi, Shiru Jia, Zhilei Tan, and Huabing Zhao. "Advances of naphthalene degradation in Pseudomonas putida ND6." In ADVANCES IN ENERGY SCIENCE AND ENVIRONMENT ENGINEERING II: Proceedings of 2nd International Workshop on Advances in Energy Science and Environment Engineering (AESEE 2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5029792.

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Dixon, D., W. Wilson, V. Steullet, and S. Takenaka. "Studies of Naphthalene Diimides as DNA-binding Agents." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02060.

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He, Fei, Akiyoshi Hanai, Hiroshi Nagamochi, and Tatsuya Akutsu. "Enumerating Naphthalene Isomers of Tree-like Chemical Graphs." In 7th International Conference on Bioinformatics Models, Methods and Algorithms. SCITEPRESS - Science and and Technology Publications, 2016. http://dx.doi.org/10.5220/0005783902580265.

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Du, Yong, Hongxia Fang, Qi Zhang, and Zhi Hong. "Terahertz spectroscopic characterization of naphthalene and 1-nitronaphthalene." In 2015 40th International Conference on Infrared, Millimeter, and Terahertz waves (IRMMW-THz). IEEE, 2015. http://dx.doi.org/10.1109/irmmw-thz.2015.7327425.

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Reports on the topic "Naphthalenone"

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Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1226965.

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Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1281678.

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Buchholz, Bruce A. Metabolic Mechanisms of Naphthalene Toxicity in Lung. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1529177.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7149929.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6884708.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6929711.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6986489.

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Ghoshal, S., A. Ramaswami, and R. G. Luthy. Biodegradation of naphthalene from coal tar. Research progress report. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10178125.

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Lotufo, Guilherme, Mandy Michalsen, Danny Reible, et al. Interlaboratory study of polyethylene and polydimethylsiloxane polymeric samplers for ex situ measurement of freely dissolved hydrophobic organic compounds in sediment porewater. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/48512.

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We evaluated the precision and accuracy of multilaboratory measurements for determining freely dissolved concentrations (Cfree) of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in sediment porewater using polydimethylsiloxane and low-density polyethylene polymeric samplers. Four laboratories exposed performance reference compound (PRC) preloaded polymers to actively mixed and static ex situ sediment for approximately one month or more. For Cfree results, intralaboratory precision was high for single compounds; most PAHs and PCBs variability was low. Variability w
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Buchholz, B. A. Mechanism for Clastogenic Activity of Naphthalene. Quarterly Technical Progress Report. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1239176.

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