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Relevant bibliographies by topics / Butadiene

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Academic literature on the topic 'Butadiene'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Butadiene"

1

Bates, Gordon S., Michael D. Fryzuk, and Charles Stone. "Convenient synthesis and cycloaddition reactions of 2-phenylseleno-1,3-butadiene and 2-trialkylstannyl-1,3-butadienes." Canadian Journal of Chemistry 65, no. 11 (1987): 2612–17. http://dx.doi.org/10.1139/v87-431.

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The facile preparation of 2-trialkylstannyl-1,3-butadienes and 2-phenylseleno-1,3-butadiene by reaction of 2-(1,3-butadienyl)magnesium chloride with trialkylstannyl chlorides and phenylselenium chloride, respectively, is reported. The Diels–Alder reactivity of these dienes with a variety of activated dienophiles is also described. Finally, a novel transmetallation of tin, in vinyl stannanes, to selenium by use of phenylselenium chloride is outlined.

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Rahmawati, Atiqa, Andri Saputra, and Uma Fadzilia. "PENGARUH PAPARAN MICROWAVE TERHADAP DERAJAT IKATAN SILANG PADA VULKANISASI KARET STIRENA." Warta Perkaretan 43, no. 1 (2024): 29–38. http://dx.doi.org/10.22302/ppk.wp.v43i1.978.

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Vulkanisasi karet diperlukan untuk meningkatkan sifat kekuatan dan elastisitas suatu produk karet. Selain mempersingkat waktu proses, kelebihan vulkanisasi menggunakan radiasi elektromagnetik dari microwave adalah panas yang seragam yang tidak tergantung pada ketebalan produk. Penelitian ini bertujuan mengetahui karakteristik vulkanisasi karet stirena butadiena pada berbagai waktu paparan radiasi microwave. Kompon karet stirena butadiena dimasukkan dalam microwave dan diberi paparan radiasi elektromagnetik menggunakan daya 5 W pada berbagai waktu (10, 30, 50, 60, dan 70 menit). Derajat ikatan

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B.L., van Drooge, Marco E., and Grimalt J.O. "Atmospheric pattern of volatile organochlorine compounds and hexachlorobenzene in the surroundings of a chlor-alkali plant." Science of the total Environment 628-629 (April 24, 2018): 782–90. https://doi.org/10.5281/zenodo.1227688.

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The outdoor atmospheric distributions of chlorinated volatile organic compounds (VOCs) from locations receiving the emissions of a chlor-alkali plant have been studied. Trichloroethylene and tetrachloroethylene (medians 2.4 µg/m<sup>3</sup> and 1.7 µg/m<sup>3</sup>, respectively) were the most abundant compounds, which was in accordance with the production processes from these installations. The concentrations of trichlorofluoromethane, median 1.6 µg/m<sup>3</sup>, are rather similar to the average levels described in general in the troposphere and cannot be attributed to thi

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B.L., van Drooge, Marco E., and Grimalt J.O. "Atmospheric pattern of volatile organochlorine compounds and hexachlorobenzene in the surroundings of a chlor-alkali plant." Science of the Total Environment 628-629 (February 20, 2018): 782–90. https://doi.org/10.1016/j.scitotenv.2018.02.088.

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The outdoor atmospheric distributions of chlorinated volatile organic compounds (VOCs) from locations receiving the emissions of a chlor-alkali plant have been studied. Trichloroethylene and tetrachloroethylene (medians 2.4 μg/m<sup>3</sup> and 1.7 μg/m<sup>3</sup>, respectively) were the most abundant compounds, which was in accordance with the production processes from these installations. The concentrations of trichlorofluoromethane, median 1.6 μg/m<sup>3</sup>, are rather similar to the average levels described in general in the troposphere and cannot be attributed to this specifi

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5

Skuratov, K. D., M. I. Lobach, A. S. Khachaturov, and V. A. Kormer. "Cis-1,4-copolymerization of butadiene and 2-alkyl butadienes." Polymer Science U.S.S.R. 29, no. 7 (1987): 1544–52. http://dx.doi.org/10.1016/0032-3950(87)90415-1.

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Hazarika, Parasa, Pallab Pahari, Manash Jyoti Borah, and Dilip Konwar. "I2-SDS-H2O System: A highly Efficient Dual Catalytic Green System for Deprotection of Imines and in Situ Preparation of Bis(indolyl)alkanes from Indoles in Water." ISRN Organic Chemistry 2012 (August 27, 2012): 1–6. http://dx.doi.org/10.5402/2012/635835.

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A novel catalytic system consisting of I2-SDS-H2O has been developed which cleaves 2,3-diaza-1,3-butadiene, 1-aza-1,3-butadienes, oximes and in presence of indoles in the medium uses the corresponding aldehyde products to produce bis(indolyl)alkanes in situ. This one pot simple and mild dual catalytic system works in water at room temperature under neutral conditions.

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Jiménez-Vázquez, Hugo Alejandro, Luis Almazán, and Adriana Benavides. "Contribution of Dispersion to the Intrinsic Energy Barriers of Neutral Model Diels-Alder Reactions." Journal of the Mexican Chemical Society 68, no. 1 (2024): 73–87. http://dx.doi.org/10.29356/jmcs.v68i1.1867.

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The intrinsic reaction coordinates for the cycloadditions between ethene and 1,3-butadiene, and ethene and cyclopentadiene, were determined at the SCS-MP2/aug-cc-pVTZ level of theory. The energy contents of the points determined for both coordinates were decomposed into their deformation and interaction contributions. From this analysis it is concluded that the higher reaction barrier for the butadiene-ethene cycloaddition can be attributed primarily to the conformational change of butadiene required by the reaction (higher deformation energy). There is also a minor contribution of the interac

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8

Wiberg, Nils, and Susanne Wagner. "Zur Reaktivität des Germaethens Me2Ge=C(SiMe3)2: Mechanistische Aspekte der Diels-Aider- und En-Reaktionen [1] / On the Reactivity of Germaethene Me2Ge=C (SiMe3)2: Mechanistic Aspects of Diels Alder and Ene Reactions [1]." Zeitschrift für Naturforschung B 51, no. 6 (1996): 838–50. http://dx.doi.org/10.1515/znb-1996-0614.

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Abstract Diels-Alder and ene reactions of germaethene Me2Ge=C(SiMe3)2 (2) with butadienes respectively, take place regioselectively, as well as stereoselectively. They are accelerated by an increasing tendency of substituents in butadiene or propene to donate electrons (e.g. 2-methylbutadiene > butadiene; 2-methylpropene > propene), and retarded by an increasing bulkyness of substituents in 1,4- or 1,3-positions (e.g. 1-methylbutadiene > 2-methylbutadiene; 1-vinylpropene > propene). It is concluded from these studies that Diels-Alder and ene reactions of 2 occur - like those of Me2

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9

Botros, S. H., A. F. Moustafa, and S. A. Ibrahim. "Homogeneous Styrene Butadiene/Acrylonitrile Butadiene Rubber Blends." Polymer-Plastics Technology and Engineering 45, no. 4 (2006): 503–12. http://dx.doi.org/10.1080/03602550600553705.

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Kantlehner, Willi, Kai Edelmann, Jochen Mezger, Markus Vettel, and Wolfgang Frey. "Orthoamide und Iminiumsalze, CIV. Umsetzungen von Orthoamiden der Alkincarbonsäuren mit enolisierbaren Carbonylverbindungen – Cyclisierung der Kondensationsprodukte zu Pyran-Derivaten." Zeitschrift für Naturforschung B 76, no. 8 (2021): 417–30. http://dx.doi.org/10.1515/znb-2021-0005.

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Abstract Orthoamides of alkynecarboxylic acid 15 condense with enolisable β-dicarbonyl compounds and as well with acetophenones to give 3-acryl-1,1-bis(dimethyl-amino)-1,3-butadienes. Some acylbutadienes cyclize affording 2-pyranon-derivatives 33 upon heating with aqueous ethanol. 2H-pyranes are accessible from acetone dicarboxylic acid ester and orthoamides 15. The constitution of one 4-acyl-1,1-bis(dimethylamino)-1,3-butadiene (16f) and one 2H-pyrane (44b) was confirmed by crystal structure determinations.

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Dissertations / Theses on the topic "Butadiene"

1

Parent, John Scott. "Catalytic hydrogenation of butadiene copolymers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq21378.pdf.

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Wilson, Joanne Patricia. "The molecular toxicology of butadiene." Thesis, University of Newcastle Upon Tyne, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.287826.

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Macqueron, Benoit. "Étude du comportement des systèmes catalytiques métallocène de néodyme / dialkylmagnésium pour la copolymérisation de l'éthylène avec le butadiène et fonctionnalisation des polymères synthétisés." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10083.

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au, D. James@murdoch edu, and Donny Lawrence James. "Biochemical Dechlorination of Hexachloro-1,3-butadiene." Murdoch University, 2010. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20100216.212048.

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Hexachloro-1,3-butadiene (HCBD) is a toxic aliphatic chlorinated hydrocarbon which is widely used as a fungicide, herbicide and heat transformer fluid. HCBD is resistant to microbial degradation and, therefore, persists in aquatic and soil environments worldwide. In this thesis, the ability of non-specific bacteria from various sources to dechlorinate HCBD in the presence of either acetate or lactate (as an electron donor) and cyanocobalamin (as an electron shuttle) under different conditions was investigated. Cultivating specific populations to reduce cyanocobalamin as a method to increase HC

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James, Donny Lawrence. "Biochemical dechlorination of hexachloro-1,3-butadiene /." Murdoch University Digital Theses Program, 2009. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20100216.212048.

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James, Donny Lawrence. "Biochemical Dechlorination of Hexachloro-1,3-butadiene." Thesis, James, Donny Lawrence (2010) Biochemical Dechlorination of Hexachloro-1,3-butadiene. PhD thesis, Murdoch University, 2010. https://researchrepository.murdoch.edu.au/id/eprint/1674/.

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Hexachloro-1,3-butadiene (HCBD) is a toxic aliphatic chlorinated hydrocarbon which is widely used as a fungicide, herbicide and heat transformer fluid. HCBD is resistant to microbial degradation and, therefore, persists in aquatic and soil environments worldwide. In this thesis, the ability of non-specific bacteria from various sources to dechlorinate HCBD in the presence of either acetate or lactate (as an electron donor) and cyanocobalamin (as an electron shuttle) under different conditions was investigated. Cultivating specific populations to reduce cyanocobalamin as a method to increase HC

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James, Donny Lawrence. "Biochemical Dechlorination of Hexachloro-1,3-butadiene." James, Donny Lawrence (2010) Biochemical Dechlorination of Hexachloro-1,3-butadiene. PhD thesis, Murdoch University, 2010. http://researchrepository.murdoch.edu.au/1674/.

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Hexachloro-1,3-butadiene (HCBD) is a toxic aliphatic chlorinated hydrocarbon which is widely used as a fungicide, herbicide and heat transformer fluid. HCBD is resistant to microbial degradation and, therefore, persists in aquatic and soil environments worldwide. In this thesis, the ability of non-specific bacteria from various sources to dechlorinate HCBD in the presence of either acetate or lactate (as an electron donor) and cyanocobalamin (as an electron shuttle) under different conditions was investigated. Cultivating specific populations to reduce cyanocobalamin as a method to increase HC

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8

Booker, Randall Sulter Jr. "Microbial reductive dechlorination of hexachloro-1,3-butadiene." Diss., Georgia Institute of Technology, 1999. http://hdl.handle.net/1853/20921.

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9

Donehue, Jessica Erin. "Excited state dynamics of 1,4-diphenyl-1,3-butadiene and 1,1,4,4-tetraphenyl-1,3-butadiene probed by time-resolved electronic spectroscopy." Connect to resource, 2009. http://hdl.handle.net/1811/37111.

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Wang, Zhao. "Selective Hydrogenation of Butadiene over Non-noble Bimetallic Catalysts." Electronic Thesis or Diss., Paris 6, 2017. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2017PA066102.pdf.

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Ce travail porte sur la préparation et la caractérisation de catalyseurs bimétalliques Cu-Zn, Ni-Zn et Fe-Zn supportés sur TiO2 avec des rapports atomiques variables et sur l'étude de leurs propriétés catalytiques pour l'hydrogénation sélective d'hydrocarbures polyinsaturés. Les méthodes de co-dépôt-précipitation à l'urée (DPu) et co-dépôt-précipitation à pH fixe (DP8) ont été utilisées pour la préparation des matériaux. Les ions métalliques se déposent séquentiellement sur la surface de TiO2 (selon la séquence CuII < ZnII ?FeII <br>This work investigates the preparation and characterizatio

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Books on the topic "Butadiene"

1

Canada, Canada Environment, Canada Health Canada, and Canada, eds. 1,3-butadiene. Environment Canada, 2000.

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2

Marja, Sorsa, World Health Organization, and International Agency for Research on Cancer., eds. Butadiene and styrene: Assessment of health hazards. International Agency for Research on Cancer, 1993.

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United States. Agency for Toxic Substances and Disease Registry, ed. Draft toxicological profile for 1,3-butadiene. U.S. Department of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 2009.

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4

T, Vermeire, WHO Task Group on Environmental Health Critera for Hexachlorobutadiene., United Nations Environment Programme, International Labour Organisation, World Health Organization, and International Program on Chemical Safety., eds. Hexachlorobutadiene. World Health Organization, 1994.

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5

National Toxicology Program (U.S.). NTP technical report on the toxicology and carcinogenesis studies of 1,3-butadiene: (CAS no. 106-99-0) in B6C3F mice (inhalation studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Toxicology Program ; Springfield, VA : Available for sale from the National Technical Information Service, U.S. Dept. of Commerce, 1993.

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6

United States. Environmental Protection Agency. Office of Air Quality Planning and Standards, ed. Locating and estimating air emissions from sources of 1,3-butadiene. Office of Air Quality and Planning Standards, Office of Air and Radiation, U.S. Environmental Protection Agency, 1996.

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7

K, Hughes, World Health Organization, International Labour Organisation, United Nations Environment Programme, International Program on Chemical Safety., and Inter-Organization Programme for the Sound Management of Chemicals., eds. 1,3-butadiene: Human health aspects. World Health Organization, 2001.

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8

Illing, H. P. A. 1,3-Butadiene and related compounds. HMSO, 1985.

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D.C.) National Center for Environmental Assessment (Washington. Health assessment of 1,3-butadiene. The Center, 2002.

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. 1,3-butadieno. Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, Agencia para Sustancias Tóxicos y el Registro de Enfermedades, 1992.

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Book chapters on the topic "Butadiene"

1

Gooch, Jan W. "Butadiene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1702.

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Gooch, Jan W. "Butadiene Rubber." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1704.

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Gooch, Jan W. "Styrene Butadiene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11338.

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Gooch, Jan W. "Methyl Butadiene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7397.

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Kaminsky, W., and R. Kramolowsky. "Butadiene Polymerization." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch116.

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Patnaik, Pradyot. "1,3-Butadiene." In Handbook of Environmental Analysis. CRC Press, 2017. http://dx.doi.org/10.1201/9781315151946-75.

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Bährle-Rapp, Marina. "Butadiene/Acrylonitrile Copolymer." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1396.

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Whelan, Tony, and John Goff. "Acrylonitrile Butadiene Styrene." In Injection Molding of Thermoplastics Materials — 1. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-0582-9_6.

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Bährle-Rapp, Marina. "Styrene/Butadiene Copolymer." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10146.

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Gooch, Jan W. "Butadiene-Acrylonitrile Copolymer." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1703.

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Conference papers on the topic "Butadiene"

1

Gomes, Jo�o P., Rodrigo Silva, Clemente Nunes, and Domingos Barbosa. "Green Solvent Alternative for Extractive Distillation of 1,3-Butadiene." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.132161.

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The separation of 1,3-butadiene from C4 hydrocarbon mixtures is a crucial step in the production of synthetic rubbers and plastics. Conventional extractive distillation methods using solvents, like N,N-dimethylformamide (DMF), have proven effective but presents significant health and environmental challenges. This study explores the feasibility of using propylene carbonate (PC) as a green solvent alternative for butadiene extractive distillation, leveraging its environmentally friendly properties and industrial compatibility. Simulations were conducted using Aspen Plus�, employing the Non-Rand

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Kass, Michael D., Christopher J. Janke, Samuel A. Lewis, James R. Keiser, and Raynella M. Connatser. "Elastomer Compatibility with a Pyrolysis-derived Bio-oil." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14613.

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Abstract The compatibility of fueling infrastructure elastomers in bio-oil and diesel fuel was determined by measuring the volume swell and hardness before and after drying. The bio-oil was produced via fast pyrolysis from a blend of pine feedstocks. The elastomer materials included two fluorocarbons, six acrylonitirile butadiene rubbers (NBRs), fluorosilicone, styrene butadiene rubber, neoprene, polyurethane, neoprene, silicone, ethylene propylene diene monomer (EPDM), hydrogenated acrylonitrile butadiene rubber (HNBR), a blend of NBR and PVC (OZO), and a blend of epichlorohydrin and ethylene

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Kass, Michael D., Christopher J. Janke, Raynella M. Connatser, James R. Keiser, Samuel A. Lewis, and Katherine Gaston. "Elastomer and Plastic Compatibility with a Pyrolysis-derived Bio-oil." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-13566.

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Abstract The compatibility of fueling infrastructure elastomers and plastics in bio-oil and diesel fuel was determined by measuring the volume swell. The bio-oil was produced via fast pyrolysis of woody feedstocks. The elastomer materials included fluorocarbons, acrylonitrile butadiene rubbers, neoprene, polyurethane, neoprene, styrene butadiene (SBR) and silicone. The plastic materials included polyphenylene sulfide (PPS), polyethylene terephthalate (PET), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), polyoxymethylene (POM), POM copolymer, high density polyethylene (HDPE), p

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Terrill, Edward, Jonathan Martens, and Yosuke Uehara. "Evaluation of Farnesene/Butadiene and Farnesene/Styrene/Butadiene Liquid Rubbers in a Silica Tread." In Technical Meeting of the Rubber Division, ACS. Rubber Division - American Chemical Society (ACS), 2023. http://dx.doi.org/10.52202/073692-0017.

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Xiong, Jianping, Aiqin Shen, JunLin Liang, and Hao Wang. "Mechanism of Butadiene-Styrene Modified Concrete." In 2012 Second International Conference on Intelligent System Design and Engineering Application (ISDEA). IEEE, 2012. http://dx.doi.org/10.1109/isdea.2012.748.

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Reffaee, Abeer S. A., D. E. El Nashar, S. L. Abd-El-Messieh, and K. N. Abd-El Nour. "Electrical and Mechanical Properties of acrylonitrile butadiene rubber / styrene butadiene rubber blends filled with carbon black." In 2007 IEEE International Conference on Solid Dielectrics. IEEE, 2007. http://dx.doi.org/10.1109/icsd.2007.4290805.

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Cândido, L. H. A., D. B. Ferreira, W. Kindlein Júnior, R. Demori, and R. S. Mauler. "Recycling cycle of materials applied to acrylonitrile-butadiene-styrene/policarbonate blends with styrene-butadiene-styrene copolymer addition." In PROCEEDINGS OF PPS-29: The 29th International Conference of the Polymer Processing Society - Conference Papers. American Institute of Physics, 2014. http://dx.doi.org/10.1063/1.4873865.

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Bisal, K. B., and Kamal K. Kar. "Exfoliated Graphite reinforced Acrylonitrile butadiene styrene Composites." In Proceedings of the International Conference on Nanotechnology for Better Living. Research Publishing Services, 2016. http://dx.doi.org/10.3850/978-981-09-7519-7nbl16-rps-95.

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ANZENGRUBER, Gertrud, and Christof LANZERSTORFER. "Remediation of Hexachloro-1,3-Butadiene Contaminated Groundwater." In Air and Water Components of the Environment 2019 Conference. Casa Cărţii de Ştiinţă, 2019. http://dx.doi.org/10.24193/awc2019_33.

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Fleitz, Paul A., Daniel G. McLean, and Richard L. Sutherland. "Nonlinear absorption in diphenyl butadiene, diphenyl butadiyne, and a series of acetylene compounds using the Z-scan technique." In SPIE's International Symposium on Optical Engineering and Photonics in Aerospace Sensing, edited by M. J. Soileau. SPIE, 1994. http://dx.doi.org/10.1117/12.179591.

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Reports on the topic "Butadiene"

1

Rutkowski, Joseph V., and Barbara C. Levin. Acrylonitrile-butadiene-styrene copolymers (ABS) :. National Bureau of Standards, 1985. http://dx.doi.org/10.6028/nbs.ir.85-3248.

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2

Thornton-Manning, J. R., A. R. Dahl, and W. E. Bechtold. Gender differences in the metabolism of 1,3-butadiene to butadiene diepoxide in Sprague-Dawley rats. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/381366.

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Wijmans, J. G., D. Alvarado, R. W. Baker, I. Pinnau, M. Rezac, and J. E. Stearns. Membrane reactor for the production of butadiene. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/763896.

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4

Klepeis, J., W. Evans, N. Zaitseva, E. Schwegler, and S. Teat. Crystallographic Information File of 1,1,tetraphenyl-1,3-butadiene. Office of Scientific and Technical Information (OSTI), 2009. http://dx.doi.org/10.2172/963124.

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Bechtold, W. E., and R. B. Hayes. Biological monitoring to determine worker dose in a butadiene processing plant. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/381369.

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Borkowsky, S., W. Tumas, and R. M. Waymouth. Transition metal catalyzed polymerization of butadiene in supercritical CO{sub 2}. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/631181.

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Dagle, Robert, and Vanessa Dagle. Production of 1,3-Butadiene from Renewable Oxygenated Feedstocks (Abstract) - CRADA 560. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1958878.

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Smith, R. E. Chemical characterization of CTBN (carboxyl-terminated butadiene/acrylonitrile) and its epoxy adduct. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/5054971.

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Hackett, P. L., M. R. Sikov, T. J. Mast, et al. Inhalation developmental toxicology studies of 1,3-butadiene in the rat: Final report. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/5664174.

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Hackett, P. L., M. R. Sikov, T. J. Mast, et al. Inhalation developmental toxicology studies: Teratology study of 1,3-butadiene in mice: Final report. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/5555439.

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