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Sakiyama T 1, Weber R 2 *, Behnisch P 3, Nakano T 4 1 Osaka City Institute of Public Health and Env. Sciences, Tohjo-cho 8-34, Tennoji- ku, Osaka 543-0026, Japan; 2 POPs Environmental Consulting, Ulmenstrasse 3, 73035 Göppingen, Germany 3 BioDetection Systems BV (BDS), Kruislaan 406, 1098 SM Amsterdam, The Netherlands, 4 Osaka University, Research Center for Environm. Preservation 2-5 Yamadaoka, Suita, Osaka 565-0871, Japan
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Dioxins and pesticide history in Japan Dioxin and pesticide screening Australia (2010) 2,4,5-T and chlorpyrifos as Twins? Chlorpyrifos as Formation of Pyridin analogue 2,3,7.8-TCDD in thermal experiments Analytical behaviour of 2,3,7.8-TCDD-Py Dioxin-like toxicity of thermal experiments Possible practical experience 2,3,7.8-TCDD-Py
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Masunaga et al. 1998 Pesticide production, use and disposal have contributed significantly to polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/F) emissions in the past.
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Formulation basis (FL) Active Ingredient basis (AI) DIOXIN IMPURITIES IN PESTICIDE FORMULATIONS UNEP Emission Factor for 2,4,5-T Holt et al. ES&T. 44, 5409–5415 (2010)
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OR In 2,4,5-T production and in product high 2,3,7,8-TCDD level 2,4,5-Trichlorphenol (R=H) 2,4,5-T (R=Essigsäure) 2,3,7,8-TCDD (Seveso-Dioxin; in Agent Orange) Cl O O O O N N OR N Chlorpyrifos (R=Phosphor acid ester) 3,5,6-trichloro-2-pyridinol (R=H)
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2,3,7,8-TCDD (Seveso Dioxin) 2,3,7,8-TCDD-pyridin-analogue 2,4,5-Trichlorophenol (R=H) 2,4,5-T (R=Acetic Acid) (in Agent Orange) Production Thermal Stress Production? Thermal Stress? Smiles Rearrangement Chlorpyrifos (R=Phosphor acid ester) 3,5,6-trichloro-2-pyridinol (R=H)
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Highest sales of chlorpyrifos of all organophosphate pesticides worldwide, and the third among all pesticides. In 2010, the consumption of chlorpyrifos globally (converted into technical) reached 80,000 tonnes with CAGR of about 12% in the past five years (2005 to 2010). Chinese production capacity was 116,000 tonnes (2010). Chlorpyrifos Chlorpyrifos-Methyl In Vietnam about 37,000 tonnes of 2,4,5-T have been sprayed in total containing 366 kg TEQ to 1123 kg TEQ (Stellmann et al., Nature 422, 681-687 (2003)
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All pyrolysis experiments were carried out in sealed brown glass ampoules (10 ml; air) with about 2 mg of respective chemical chlorpyrifos, chlorpyrifos-methyl and the major degradation product of chlorpyrifos, 3,5,6-trichloro-2- pyridinol (TCPy) at temperatures between 300ºC and 380ºC. Chlorpyrifos Chlorpyrifos-Methyl Analytical grade chlorpyrifos, TCPy (both Dr. Ehrenstorfer GmbH, Augsburg/Germany) and chlorpyrifos-methyl (Wako Pure Chemicals, Osaka/Japan) were used.
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Relative abundance of 2,3,7,8-TCDD-pyridine-analogues formed in thermal experiments (ampoule; air;15 min) 2378-TCDD-pyridine- analogue (1)* 2378-TCDD-pyridine- analogue (2)** 300ºC340ºC380ºC 300ºC340ºC380ºC chlorpyrifos001x10^5003x10^5 chlorpyrifos- methyl 006x10^5003x10^6 3,5,6-trichloro-2- pyridinol 1x10^56x10^63x10^7 1x10^51x10^71x10^8 *trans-isomer of 2,3,7,8-TCDD-Py; **cis-isomer of 2,3,7,8-TCDD-Py
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2,3,7,8-TCDD- N-analogues TriCDD N-analogue TriCDD N-analogues DiCDD N-analogue 2,3,7,8-TCDD N-analogues PentaCDD N-analogue
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The 2,3,7,8-TCDD-Py does not elute gogether with PCDD/PCDF in the following clean-up columns: (mention which columns The Pyridin-analogues as base are adsorbed on the column and need specific elution in the clean-up Therefore PCDD-Py are not transfered to GC/MS with (most?) current clean-up columns and would therefore not be detected in GC/MS (even in scan mode).
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Dioxin-like toxicities were assessed with the DR-CALUX TM assay. Extremely high dioxin-like toxicity was detected from the treatment at 380ºC of TCPy (143,000 ng 2,3,7,8-TCDD bio-TEQ/g treated TCPy). The 48 h kinetic indicated that the dioxin-like active compounds were stable.
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2,3,7,8-TCDD-Py (having dioxin-like toxicity) is formed from chlorpyrifos, chlorpyrifos-methyl and in particular their major degradation product (TCPy) in heating experiments highlighting the need to investigate the formation of 2,3,7,8-TCDD-Py in real world scenarios with thermal stress e.g. cigarette smoking (chlorpyrifos used in tobacco cultivation) the combustion of post-harvest residues fires in pesticide production or storage.
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Furthermore, 2,3,7,8-TCDD-Py is a high volume pesticide used for e.g. should be screened in chlorpyrifos pesticide formulations. With the background that 2,4,5-TCP based pesticides (Agent Orange, Pink, Purpule, White contained extreme high 2,3,7,8-TCDD levels). Such assessments should include bio-assays for quantitative toxicity information on the extent of dioxin-like activity considering that also compounds other then 2,3,7,8-TCDD-Py seem to have dioxin-like activity in thermal treatment of chlorpyrifos.
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Assessment: PFOA, PFXSi, PFHxS DeBDE,HBCDD,PBB, PBDD/F, HBBz, PBP, TBBPA, TBPAE, SCCP, MCCP, PCN, HCBD, OCS, PCP, PCNB PAHs, Nitro-PAH Halogenated PAHs PT-Pesticides, PT-Biocides PT-Pharmaceuticals PT-Siloxanes Sn-Organics Hg, Cd. Pb et al. PCDD PCDF PCBs Dieldrin Aldrin DDT PCB HCB Chlordane Heptachlor Mirex Toxaphene Endrin “The dirty dozen” www.pops.int www.saicm.org www.ipen.org http://www.springerlink.com/content/0q10km8582605r1x/fulltext.pdf http://www.springerlink.com/content/0q10km8582605r1x/fulltext.pdf “The nasty nine” alpha-, beta-, gamma-HCH, PeCB, Chlordecone, PeBDE, OBDE, HBB, PFOS Evil Endo sulfan
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Litres of herbicides sprayed over 1962–1971. The data are taken from the corrected HERBS file Stellmann et al., Nature 422, 681-687 (2003)
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