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Muller F et al; Ullmann's
Encyclopedia of Industrial Chemistry 7th ed. (1999-2012). NY, NY: John Wiley & Sons; Fungicides, Agricultural, 2. Individual Fungicides. Online Posting Date: October 15, 2011
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Etridiazole is stable under normal conditions, but degrades upon continuous exposure to sunlight, and is hydrolysed by alkalis. When heated to decomposition, it emits toxic fumes of
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Spencer, E. Y. Guide to the
Chemicals Used in Crop Protection. 7th ed. Publication 1093. Research Institute, Agriculture Canada, Ottawa, Canada: Information Canada, 1982., p. 279
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It can also be is produced by the reaction of trichloroacetamidine hydrochloride with trichloromethanesulfenyl chloride, and then with sodium hydroxide in ethanol.
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Worthing, C.R., S.B. Walker (eds.). The
Pesticide Manual - A World Compendium. 7th ed. Lavenham, Suffolk, Great Britain: The Lavenham Press Limited, 1983., p. 252
821:
USEPA Office of
Pesticide Programs, Health Effects Division, Science Information Management Branch: "Chemicals Evaluated for Carcinogenic Potential" (April 2006)
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Lewis, R.J. Sr. (ed) Sax's
Dangerous Properties of Industrial Materials. 11th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2004., p. 1623
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Do not translate text that appears unreliable or low-quality. If possible, verify the text with references provided in the foreign-language article.
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Tomlin, C.D.S. (ed.). The
Pesticide Manual - World Compendium. 10th ed. Surrey, UK: The British Crop Protection Council, 1994., p. 420
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MacBean C, ed; e-Pesticide Manual. 15th ed., ver. 5.1, Alton, UK; British Crop
Protection Council. Etridazole (2593-15-9) (2008-2010)
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Content in this edit is translated from the existing German
Knowledge (XXG) article at ]; see its history for attribution.
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Pure samples are colourless and odourless; impure samples take on a pale yellow appearance with a mild, persistent odour
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Etridiazole has been classified as a Group B2 Probable Human
Carcinogen.
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Except where otherwise noted, data are given for materials in their
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InChI=1S/C5H5Cl3N2OS/c1-2-11-4-9-3(10-12-4)5(6,7)8/h2H2,1H3
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162:5-Ethoxy-3-(trichloromethyl)-1,2,4-thiadiazole
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113:{{Translated|de|Etridiazol}}
620:or concentration (LD, LC):
579:0.011 mmHg/1.43 Pa at 25°C
124:Knowledge (XXG):Translation
83:will aid in categorization.
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58:Machine translation, like
848:Trichloromethyl compounds
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443:CCOC1=NC(=NS1)C(Cl)(Cl)Cl
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640:2000 mg/kg (mouse, oral)
680:used for prevention of
122:For more guidance, see
638:1028 mg/kg (rat, oral)
95:copyright attribution
158:Preferred IUPAC name
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506: g·mol
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658:Infobox references
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169:Identifiers
138:Etridiazole
99:edit summary
90:
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670:Etridiazole
632:median dose
618:Lethal dose
608:Flash point
556:0.117 g dm
511:Appearance
452:Properties
268:100.018.175
230:CHEBI:81761
838:Fungicides
832:Categories
744:References
716:Reactivity
499:Molar mass
366:9F8237I875
241:ChemSpider
197:3D model (
176:CAS Number
692:Synthesis
678:pesticide
674:fungicide
281:EC Number
186:2593-15-9
117:talk page
69:Consider
37:in German
688:plants.
602:Hazards
93:provide
585:Acidity
520:Density
333:PubChem
324:C014547
115:to the
97:in the
39:.
736:Safety
728:, and
686:cotton
504:247.52
436:SMILES
307:C18460
152:Names
672:is a
597:2.27
569:3.37
414:InChI
346:17432
250:16489
221:ChEBI
199:JSmol
60:DeepL
676:and
562:log
357:UNII
318:MeSH
298:KEGG
91:must
89:You
53:View
684:on
383:EPA
336:CID
62:or
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489:O
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483:N
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