Relevant bibliographies by topics / Dichloropropane

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

Academic literature on the topic 'Dichloropropane'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 February 2023

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Journal articles on the topic "Dichloropropane"

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Zebarth, B. J., S. Y. Szeto, B. Hii, H. Liebscher, and G. Grove. "Groundwater Contamination by Chlorinated Hydrocarbon Impurities Present in Soil Fumigant Formulations." Water Quality Research Journal 33, no. 1 (1998): 31–50. http://dx.doi.org/10.2166/wqrj.1998.003.

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Abstract Groundwater contamination of the Abbotsford aquifer by 1,2-dichloropropane (1,2-DCP) was reported previously. The purpose of the present study is to quantify groundwater contamination by other chlorinated hydrocarbon compounds which are present in fumigant formulations containing 1,2-DCP. Widespread contamination of 1,2,2-trichloropropane (1,2,2-TCP) was measured consistent with a non-point source. 1,2,2-TCP concentration generally decreased with depth suggesting a surface source. Localized contamination by 1,2,3-trichloro-propane, 2,3-dichloropropene and 1,3-dichloropropane was detected. Detection of these compounds was associated with higher concentrations of 1,2-DCP suggesting contamination by these compounds may have been from the same fumigant sources. The lack of a decrease in the concentration of most of these compounds over time suggests that the measured contamination will persist for some time. The results highlight the potential for persistent trace impurities in chlorinated fumigant formulations to contaminate groundwater in vulnerable aquifers.
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Merriman, John C., John Struger, and Richard S. Szawiola. "Distribution of 1,3-dichloropropene and 1,2-dichloropropane in big Creek watershed." Bulletin of Environmental Contamination and Toxicology 47, no. 4 (1991): 572–79. http://dx.doi.org/10.1007/bf01700948.

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Crowder, G. A. "Vibrational analysis of 2,2-dichloropropane and 2,2-dichloropropane-d6." Spectrochimica Acta Part A: Molecular Spectroscopy 42, no. 9 (1986): 1079–82. http://dx.doi.org/10.1016/0584-8539(86)80022-8.

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Pérez, P., J. Valero, M. Gracia, and C. Gutiérrez Losa. "GmE(298.15 K) of mixtures containing 1,2-dichloropropane or 1,3-dichloropropane." Journal of Chemical Thermodynamics 21, no. 3 (1989): 259–64. http://dx.doi.org/10.1016/0021-9614(89)90015-3.

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Baños, I., J. Valero, P. Pérez, M. Gracia, and C. Gutiérrez Losa. "Excess molar volumes of mixtures containing 1,2-dichloropropane or 1,3-dichloropropane." Journal of Chemical Thermodynamics 22, no. 5 (1990): 431–37. http://dx.doi.org/10.1016/0021-9614(90)90133-b.

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Grove, Gary, Sunny Y. Szeto, Hugh Liebscher, Basil Hii, and Bernie J. Zebarth. "Occurrence of 1,2-Dichloropropane and 1,3-Dichloropropene in the Abbotsford Aquifer, British Columbia." Water Quality Research Journal 33, no. 1 (1998): 51–72. http://dx.doi.org/10.2166/wqrj.1998.004.

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Abstract Forty piezometers at 13 sites in the Canadian portion of the Abbotsford aquifer were tested for 1,2-dichloropropane (1,2-DCP) and 1,3-dichloropropene (1,3-DCP) on an approximate monthly interval from July 1991 to June 1994. Detectable levels of 1,2-DCP were found in 32 of the 40 piezometers. Average 1,2-DCP concentrations within a piezometer ranged up to 2.23 µg/L and a maximum concentration of 7.07 µg/L was recorded in one piezometer. 1,3-DCP was detected for only a short period of time in one piezometer and at a maximum concentration of 0.23 µg/L. 1,2-DCP contamination in the aquifer is attributed to application of fumigants containing this compound as an active ingredient or as an impurity for the control of root nematodes in red raspberry crops. The nature of the contamination is consistent with a non-point source that is highly variable in space and time. Although soil fumigants containing 1,2-DCP as an active ingredient are no longer used in the Abbotsford area, fairly constant values of 1,2-DCP would indicate there is still a contaminant source providing input to the groundwater. 1,2-DCP has apparently accumulated on the soil sediments above the water table and is slowly being released to the groundwater. In the top 15 m of the saturated zone, concentrations generally decreased with depth below the water table to near nondetectable levels. Correlation between contaminant levels and rainfall or other environmental factors that might affect the distribution of 1,2-DCP could not be established. More detailed soil measurements and controlled laboratory experiments are needed to determine 1,2-DCP movement as well as rates of dissipation in the Abbotsford aquifer.
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Trevisan, Andrea, Stefano Maso, and Paola Meneghetti. "Renal Cortical Slices: An In Vitro Model for Kidney Metabolism and Toxicity." Alternatives to Laboratory Animals 20, no. 1 (1992): 71–76. http://dx.doi.org/10.1177/026119299202000110.

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The in vitro renal cortical slice model was used to study: 1) the effects on the kidney of some haloalkanes and haloalkenes using 3-month-old male Wistar rats; 2) influence of age and sex on renal cortical slice indices in non-treated rats; and 3) effects of 1,2-dichloropropane on the slices after pretreatment of 3-month-old male Wistar rats with DL-butathionine-[S,R]-sulphoximine. The most nephrotoxic chemical used was 1,3-dichloropropene, which caused a total depletion in the levels of reduced glutathione, a high peroxidation of lipid (about three thousand-fold with respect to control), a significant release of tubular enzymes into the medium, and loss of organic anion ( p-aminohippurate) accumulation. All the chemicals affected the cytosol more than the brush border. The most remarkable age-related differences in the untreated slices were the progressive decrease of reduced glutathione (p<0.05 from three months of age), and an increase in lactate dehydrogenase release into the medium (p<0.05 from six months of age). By contrast, sex differences were slight. The ‘treatment with 1,2-dichloropropane of slices prepared from rats pretreated with DL-butathionine-[S,R]-sulphoximine significantly increased the depletion of glutathione content (p<0.05) and malondialdehyde release in the medium (p<0.001) caused by the solvent alone.
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Honma, T. "Toxicity of 1, 2-dichloropropane." SANGYO EISEIGAKU ZASSHI 40, Special (1998): 712. http://dx.doi.org/10.1539/sangyoeisei.kj00001990533.

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Trevisan, Andrea, Paola Meneghetti, Stefano Maso, and Ornella Troso. "In-Vitro Mechanisms of 1,2-Dichloropropane Nephrotoxicity using the Renal Cortical Slice Model." Human & Experimental Toxicology 12, no. 2 (1993): 117–21. http://dx.doi.org/10.1177/096032719301200204.

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1 Renal cortical slices isolated from the kidneys of male Wistar rats were used as an experimental model for studying the nephrotoxicity induced by 1,2-dichloropropane. 2 The solvent causes a depletion of renal reduced glutathione content and slight, but significant, lipid peroxidation. The block of the oxidative pathway with carbon monoxide prevents glutathione content depletion, and shows that this conjugation is the major step in 1,2-dichloropropane metabolism. 3 Loss of organic anion accumulation and release into the incubation medium of tubular enzymes, mainly from the soluble fraction, are the toxic effects of the solvent. The brush border is only slightly affected. 4 The mechanism of nephrotoxicity appears to occur via mercapturic acid metabolism. Acivicin and aminooxyacetic acid, inhibitors of gammaglutamyltransferase and β-lyase activity, respectively, partially but significantly prevent the loss of organic anion accumulation induced by 1,2-dichloropropane. Furthermore, α-ketobutyrate, an activator of β-lyase, enhances the effects of 1,2-dichloropropane on the target, but is itself toxic for organic anion accumulation.
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Tornero-Velez, Rogelio, Matthew K. Ross, Courtney Granville, et al. "METABOLISM AND MUTAGENICITY OF SOURCE WATER CONTAMINANTS 1,3-DICHLOROPROPANE AND 2,2-DICHLOROPROPANE." Drug Metabolism and Disposition 32, no. 1 (2004): 123–31. http://dx.doi.org/10.1124/dmd.32.1.123.

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Dissertations / Theses on the topic "Dichloropropane"

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Schlötelburg, Cord. "Mikrobielle Diversität und Dynamik einer 1,2-Dichlorpropan dechlorierenden Mischkultur." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2002. http://dx.doi.org/10.18452/14678.

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Die toxische sowie kanzerogene Verbindung 1,2-Dichlorpropan (DCP) ist weit verbreitet in Industrie und Landwirtschaft. Die Verbindung zeigt eine geringe chemische Reaktivität, ist nur mäßig wasserlöslich und unter aeroben Bedingungen weitestgehend beständig gegenüber mikrobiellen Abbauprozessen in der Umwelt. Als Folge reichert sich DCP in Grundwässern, Sedimenten und Böden an und gefährdet über die Nahrungskette die Gesundheit von Mensch und Tier. Um DCP effizient und ökonomisch zu unbedenklichen Verbindungen abzubauen, wurden mikrobielle Mischkulturen aus belasteten Sedimenten angereichert und in einen Wirbelschichtreaktor überführt. Dieses Verfahren ermöglichte eine kontinuierliche anaerobe Dechlorierung von DCP zu Propen. Grundsätzlich stellen biologische Abbauverfahren, bei denen komplexe mikrobielle Mischpopulationen eingesetzt werden, einen vielversprechenden Weg zur Transformation chlororganischer Verbindungen dar. Jedoch liegen üblicherweise nur wenige Informationen über die Zusammensetzung der betreffenden Populationen vor, so daß eine Optimierung bzw. effiziente Steuerung des Prozesses erheblich erschwert wird. Gegenstand der vorliegenden Arbeit war die Bestimmung der mikrobiellen Zusammensetzung der DCP-dechlorierenden Bioreaktorpopulation. Aufgrund der bekannten Limitierungen klassisch-mikrobiologischer Nachweisverfahren wurde eine Kombination mehrerer molekulargenetischer Methoden eingesetzt, die auf der vergleichenden Sequenzanalyse ribosomaler RNA beruhten. Die Untersuchungen zeigten, daß die Bakterienpopulation des Reaktors außerordentlich divers zusammengesetzt war und im wesentlichen aus bislang nicht-kultivierten Arten bestand. Es dominierten "Grüne nicht-schwefelhaltige Bakterien" (green nonsulfur bacteria) sowie Grampositive Bakterien mit niedrigem GC-Gehalt. Die Archaea hingegen waren fast ausschließlich durch zwei bekannte methanogene Spezies vertreten, Methanosaeta concilii sowie Methanomethylovorans hollandica. Der Vergleich der gewonnenen rDNA-Daten mit denen anderer Lebensräume ergab, daß Süßwasserhabitate, in denen chlororganische Verbindungen reduktiv umgesetzt werden, offenbar eine spezifische Populationsstruktur aufweisen. Es konnten spezifische 16S rDNA-Gruppen definiert werden (SHA-Cluster), die auch nach längerem Reaktorbetrieb noch nachgewiesen werden konnten. Darüber hinaus wurden Dehalobacter restrictus- sowie Dehalococcoides ethenogenes-ähnliche Bakterien in der DCP-dechlorierenden Bioreaktorpopulation gefunden. Beide Spezies sind in der Lage, chlororganische Verbindungen unter Verwendung von Wasserstoff als alleinigem Elektronendonor reduktiv zu dechlorieren. Es ist davon auszugehen, daß Dehalobacter und Dehalococcoides spp. aufgrund ihrer Physiologie an der reduktiven Umsetzung des DCPs beteiligt sind. Die Untersuchung der Population über einen längeren Zeitraum zeigte überdies, daß Bakterien der Gattung Dehalobacter überproportional angereichert und daraufhin zur dominierenden Spezies im Reaktor wurden. Dieser Befund läßt auf eine zentrale Rolle von Dehalobacter spp. bei der Transformation von DCP zu Propen schließen. Konsequenterweise führte die Zugabe von Wasserstoff zum Reaktor zur einer deutlichen Steigerung des DCP-Umsatzes. Dehalobacter und Dehalococcoides spp. sowie die anderen durch SHA-Cluster repräsentierten Bakterien stellen potentielle Indikatororganismen für die DCP-Transformation im Reaktor dar. Ein kontinuierliches Monitoring dieser Bakterien würde zu einer effizienteren Steuerung des Dechlorierungsprozesses und damit zu einer Optimierung des Verfahrens führen.
The toxic and carcinogenic compound 1,2-dichloropropane (DCP) is widely used in industry and agriculture. DCP shows a low chemical reactivity. It is only moderately soluble in aqueous systems and almost recalcitrant to microbial degradation under aerobic conditions. As a consequence DCP accumulates in groundwater, sediments and soil, thus endangering humans and animals via the food chain. To efficiently transform DCP to harmless organic compounds microbial mixed cultures have been enriched from sediments and were subsequently transferred into a fluidized bed bioreactor. This process allowed a continuous anaerobic dechlorination of DCP to propene. Bioreactor processes using complex microbiota represent a promising technology for transformation of chlorinated compounds. However, the composition of the used population is usually unknown, hence hindering both optimization and control of the degradation process. Subject of this work was the analysis of the microbial diversity of the DCP-dechlorinating bioreactor population. Conventional culture-dependent microbiological methods are often limited if used for the analysis of complex communities. Therefore, a combination of different molecular methods based on comparative 16S rRNA analysis was applied. It was found that the bioreactor population was highly diverse and consisted mainly of as yet-uncultured bacteria. Members of the green nonsulfur bacteria and the gram-positive bacteria with low G+C content dominated the consortium. In contrast the archaea were represented by only two species, Methanosaeta concilii and Methanomethylovorans hollandica. The comparison of the rDNA data with those of other biotopes revealed that reductively dechlorinating freshwater habitats show a specific community structure. 16S rDNA-clusters were defined, which could still be detected after a longer operation time of the bioreactor. Furthermore, Dehalobacter restrictus- and Dehalococcoides ethenogenes-like bacteria were found in the DCP-dechlorinating bioreactor population. Both species are capable of reductive dechlorination using hydrogen as the sole electron source. Therefore, it could be assumed that these bacteria were also involved in the dechlorination of DCP. The investigation of the bioreactor population for a longer period of time revealed that Dehalobacter-like bacteria were significantly enriched and subsequently became the most frequently found bacterium within the bioreactor. This indicates a major role of Dehalobacter spp. within the transformation process of DCP to propene. Consequently, the addition of hydrogen to the bioreactor led to an increase of the DCP transformation rate. Dehalobacter und Dehalococcoides spp. as well as the bacteria represented by the specific SHA-clusters are possibly suitable as indicator organisms for the transformation of DCP within the bioreactor. A continuous monitoring of these bacteria would lead to a more efficient control and hence, to an optimization of the transformation process.
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Minnis, Stephen T. "Distribution of potato cyst nematodes in England and Wales and the use of 1,3-dichloropropene for their control." Thesis, Open University, 2000. http://oro.open.ac.uk/58068/.

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In the UK the most problematic pests of the potato crop are the potato cyst nematodes Globodera rostochiensis and G. paUida. A structured survey of potato growing land in England and Wales was undertaken to reassess their occurrence and distribution. peN were present in 64% of sites sampled and of the populations found, 67% were G. pallida, 8% were G. rostochiensis and 25% contained both species. Just over 50% of the sites sampled had a rotation length of 1 in 5 or less and cultivars with partial resistance to G. paUida represented only 6% of the total number of plantings while those with resistance to G. rostochiensis represented 43%. The results show an increase in the incidence of peN compared with previous surveys and confirm the perceived shift towards G. paUida as the predominant species. Two field experiments were done to look at the integration of methods for the control of peN and subsequent reduction in yield loss in situations of very high peN levels. The first experiment assessed the use of 1,3-dichloropropene (1,3-D) with the granular nematicides aldicarb, oxamyl and fosthiazate when growing the susceptible cultivar Estima. The second experiment assessed the use of the resistant cultivar Sante with 1,3-D and oxamyl at full and half-rates. 1,3-D significantly advanced emergence, increased percentage ground cover, root invasion, yield, tuber numbers, and improved tuber size distribution. Nematode multiplication was significantly reduced by fumigation in the first experiment. The use of 1,3-D for the control of weed seeds was assessed and the results show a reduction in germination of weed seeds in soil after fumigation. The use of 1,3-D for the control of Rhizoctonia solani was also assessed and a trend in reduction in R. solani was observed after fumigation although the differences were not statistically significant.
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LAMASTRA, LUCREZIA. "Le caratteristiche ambientali di selezionate alternative chimiche all'uso del Metil Bromuro come geodisinfestante: 1,3- Dicloropropene e Cloropicrina." Doctoral thesis, Università Cattolica del Sacro Cuore, 2011. http://hdl.handle.net/10280/976.

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La produzione e l’uso del Metile di Bromuro, un fumigante estesamente usato in agricoltura, sono stati sottoposti a severe restrizioni dovute alla sua azione di depletore dello strato di ozono. Questa tesi è rivolta ad indagare il destino e le caratteristiche ambientali di due tra le più importanti alternative chimiche all’uso del Bromuro di Metile: l’ 1,3-Dicloropropene (1,3-D) e la Cloropicrina (CP). 1,3-D è un fumigante del suolo, con spiccata attività nematocida, consistente di due isomeri (Z), e (E)-1,3-D; nella sua formulazione sono presenti, inoltre, un esteso numero di impurezze clorurate potenzialmente correlate al processo produttivo. In laboratorio, è stato effettuato uno studio per valutare la stabilità idrolitica delle impurezze clorurate e per prevederne, quindi, il destino ambientale. Allo stesso tempo un piano di monitoraggio è stato svolto per valutare il leaching dell’1,3-D, dei suoi metaboliti, e delle impurezze clorurate. La CP è anch’essa un fumigante del suolo, caratterizzato da un importante profilo tossicologico. Questo lavoro ha valutato l’esposizione degli operatori e l’emissione in atmosfera durante e dopo l’applicazione nel suolo, secondo le pratiche agronomiche vigenti. Infine tramite l’applicazione di modelli matematici quali FOCUS PELMO e FOCUS PEARL si è valutato il destino ambientale della CP rispetto alle acque di falda. La simulazione è stata eseguita in 5 scenari europei realistici.
Production and use of methyl bromide, a soil fumigant, are being restricted because of this chemical’s deleterious effects on stratospheric ozone concentrations. This research examines the environmental fate and properties of methyl bromide replacement: 1,3-Dichloropropene (1,3-D), and Chloropicrin (CP). 1,3-D is a broad-spectrum soil fumigant used to control numerous species of soil-borne plant-parasitic nematodes. 1,3-D consists of two isomers, (Z)- and (E)-1,3-D, and has a number of low-level chlorinated compounds that could potentially be part of the manufacturing process. This study has investigated the hydrolytic stability, under biotic and abiotic conditions, of an extensive representative list of 1,3-D potentially related chlorinated compounds. Furthermore, a monitoring programme was carried out to investigate the leaching of all of this compounds. CP is a broad-spectrum fumigant chemical which is extensively used in agriculture and has an important toxicological profile. This study has assessed CP emission in the atmosphere and operator exposure during and after application in soil through injection of the test substances with routine agronomical application. Finally the environmental fate of CP and its metabolite dichloronitromethane in groundwater were investigated through the use of simulation model FOCUS PELMO and FOCUS PEARL using fully justified input parameters in five realistic scenarios.
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Ahubelem, Nwakamma. "Formation of toxic compounds in the thermal decomposition of 1,3-dichloropropene." Thesis, 2016. http://hdl.handle.net/1959.13/1311967.

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Research Doctorate - Doctor of Philosophy (PhD)
The formation of chlorobenzenes from oxidative thermal decomposition of 1,3-dichloropropene have been investigated using a combined combustion experiments and quantum chemical calculations. Experimental and computational results elucidate the chemistry of formation of toxic compounds from combustion chlorinated pesticides as could occur in bush fires or accidental fires of such chemicals in their storage facilities. Mono- to hexa-chlorobenzenes were observed between 800 – 1150 K, and the extent of chlorination was proportional to the combustion temperature. Higher chlorinated congeners of chlorobenzene (tetra-, penta-, hexa-chlorobenzene) were only observed in trace amounts between 950 – 1050 K. DFT calculations indicated that cyclisation of chlorinated hexatrienes proceeds via open-shell, radical pathways. Oxidation of phenylvinyl radical intermediates and subsequent ring closure were the key mechanistic pathways in the formation of benzofuran and chlorobenzofuran. Quantum chemical molecular dynamics (QM/MD) at 1,500 and 3,000 K revealed that the thermal oxidation of 1,3-dichloropropene was initiated by (1) abstraction of allylic H/Cl by O₂ and (2) intra-annular C-Cl bond scission and elimination of allylic Cl. A kinetic analysis showed that (2) is the more dominant initiation pathway, in agreement with QM/MD results. These QM/MD simulations revealed new routes to the formation of major products (H₂O, CO, HCl, CO₂), which were propagated primarily by the chloroperoxy (ClO₂), OH and 1,3-dichloropropene derived radicals. In particular, intra-annular C-C/C-H bond dissociation reactions of intermediate aldehydes/ketones were shown to play a dominant role in the formation of CO and CO₂. QM/MD simulations demonstrated that both combustion temperature and radical concentration can influence the product yield, however not the combustion mechanism. In order to elucidate the dehydrochlorination kinetics of 1,3-dichloropropene and related compounds, the unimolecular HCl elimination reactions of 1,3-dichloropropene and other chloroaliphatic hydrocarbons were investigated using high level computational chemistry methods. Two generic pathways for the elimination of HCl was found. The first involves a C-Cl fission at an allylic site and a C-H cleavage at a vinylic site, whereas the second entails scissions of allylic Cl and methylenic H. The latter pathway appears more favourable from thermodynamic and kinetic standpoints. The effect of the length of carbon chain on reaction and activation enthalpies was also investigated by considering analogous dehydrochlorination pathways for short chlorinated aliphatics (i.e., C₃, C₄), discovering the reaction and activation enthalpies required for HCl elimination to be independent of the length of the carbon chain. Dehydrochlorination reactions investigated exhibited a pressure-independent behaviour even under ambient pressure and results suggest that electronic factors rather than anchimeric assistance influence dehydrochlorination reactions of substituted ethyl halides.
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Books on the topic "Dichloropropane"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 1,2-jikuroropuropan: 1,2-Dichloropropane. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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B, Terrill James, and United States. Environmental Protection Agency., eds. The Subacute and subchronic oral toxicity of 1,3-dichloropropane in the rat. U.S. Environmental Protection Agency, 1992.

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United, States Environmental Protection Agency Prevention Pesticides and Toxic Substances. Reregistration eligibility decision: 1,3-dichloropropene, list A, case 0328. U.S. Environmental Protection Agency, Prevention, Pesticides, and Toxic Substances, 1998.

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Dichloropropane (1,3), Dichloropropane (1,2) (Health & Safety Guide). World Health Organization, 1992.

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International Program on Chemical Safety., International Labour Organisation, World Health Organization, and United Nations Environment Programme, eds. 1,3-dichloropropene, 1,2-dichloropropane and mixtures health and safety guide. World Health Organization, 1992.

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1, 3-Dichloropropene, 1,2-Dichloropropane and Mixtures (Environmental Health Criteria Series No. 146). World Health Organization, 1993.

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Annette, Ashizawa, United States. Agency for Toxic Substances and Disease Registry., Syracuse Research Corporation, and United States. Environmental Protection Agency., eds. Draft toxicological profile for dichloropropenes. U.S. Dept. of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 2006.

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Reregistration eligibility decision: 1,3-dichloropropene, list A, case 0328. U.S. Environmental Protection Agency, Prevention, Pesticides, and Toxic Substances, 1998.

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Reregistration eligibility decision: 1,3-dichloropropene, list A, case 0328. U.S. Environmental Protection Agency, Prevention, Pesticides, and Toxic Substances, 1998.

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Book chapters on the topic "Dichloropropane"

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Ware, George W. "1,2-Dichloropropane." In Reviews of Environmental Contamination and Toxicology. Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4613-8785-5_8.

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Wohlfarth, Christian. "Refractive index of 1,2-dichloropropane." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_92.

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Wohlfarth, Christian. "Refractive index of 1,3-dichloropropane." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_93.

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Wohlfarth, Ch. "Refractive index of 1,3-dichloropropane." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_59.

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Gorzka, Zbigniew, Marek Kaźmierczak, and Andrzej Żarczyński. "Catalytic Oxidation of 1,2-Dichloropropane on Copper-Zinc Catalyst." In Chemistry for the Protection of the Environment 3. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-9664-3_17.

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Wohlfarth, Christian. "Refractive index of binary liquid mixture of nitromethane and 1,3-dichloropropane." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_468.

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Wohlfarth, Christian. "Refractive index of binary liquid mixture of nitroethane and 1,3-dichloropropane." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_534.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture 1,2-Dichloropropane C3H6Cl2 + C6H6 Benzene (LB2263, VMSD1211)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_681.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture 1,3-Dichloropropane C3H6Cl2 + C6H6 Benzene (LB2262, VMSD1211)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_682.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture 1,2-Dichloropropane C3H6Cl2 + C6H12 Cyclohexane (LB2259, VMSD1211)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_701.

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Conference papers on the topic "Dichloropropane"

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Xie, Fei, Wenhua Song, Lingyue Lv, and Zhen Chen. "FDS Simulation of the Pool Fire in the Dichloropropane Tank." In 2012 4th International Conference on Multimedia Information Networking and Security (MINES). IEEE, 2012. http://dx.doi.org/10.1109/mines.2012.111.

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Lueong, S., S. Villar, V. Cahais, et al. "PO-319 Mutational signatures of 1,2-dichloropropane and dichloromethane identified in mouse carcinogenicity assays." In Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.349.

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Xie, Fei, Wenhua Song, Zhen Chen, and Lingyue Lv. "The Applied Research of Thomas Model in the Pool Fire Risk Assessment in Fire Embankment of Dichloropropane Storage Tank Area." In 2012 4th International Conference on Multimedia Information Networking and Security (MINES). IEEE, 2012. http://dx.doi.org/10.1109/mines.2012.218.

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Reports on the topic "Dichloropropane"

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NIOSH skin notation (SK) profile: 1,3-dichloropropene (1,3-D) [CAS No. 542-75-6]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2011. http://dx.doi.org/10.26616/nioshpub2011155.

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Soil analyses for 1,3-dichloropropene (1,3-DCP), sodium n-methyldithiocarbamate (metam-sodium), and their degradation products near Fort Hall Idaho, September 1999 through March 2000. US Geological Survey, 2001. http://dx.doi.org/10.3133/wri014052.

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