Etridiazole
You can help expand this article with text translated from the corresponding article in German. (August 2015) Click [show] for important translation instructions.
- View a machine-translated version of the German article.
- Machine translation, like DeepL or Google Translate, is a useful starting point for translations, but translators must revise errors as necessary and confirm that the translation is accurate, rather than simply copy-pasting machine-translated text into the English Wikipedia.
- Consider adding a topic to this template: there are already 1,848 articles in the main category, and specifying
|topic=
will aid in categorization. - Do not translate text that appears unreliable or low-quality. If possible, verify the text with references provided in the foreign-language article.
- You must provide copyright attribution in the edit summary accompanying your translation by providing an interlanguage link to the source of your translation. A model attribution edit summary is
Content in this edit is translated from the existing German Wikipedia article at [[:de:Etridiazol]]; see its history for attribution.
- You may also add the template
{{Translated|de|Etridiazol}}
to the talk page. - For more guidance, see Wikipedia:Translation.
Names | |
---|---|
Preferred IUPAC name 5-Ethoxy-3-(trichloromethyl)-1,2,4-thiadiazole | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChemSpider |
|
ECHA InfoCard | 100.018.175 |
EC Number |
|
KEGG |
|
MeSH | C014547 |
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C5H5Cl3N2OS |
Molar mass | 247.52 g·mol−1 |
Appearance | Pure samples are colourless and odourless; impure samples take on a pale yellow appearance with a mild, persistent odour |
Density | 1.497 g cm−3 [1] |
Melting point | 22 °C (72 °F; 295 K) |
Boiling point | 95 °C (203 °F; 368 K) at 1 mmHg |
Solubility in water | 0.117 g dm−3 |
log P | 3.37 |
Vapor pressure | 0.011 mmHg/1.43 Pa at 25°C |
Acidity (pKa) | 2.27 |
Hazards | |
Flash point | 154.5 °C (310.1 °F; 427.6 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) | 1028 mg/kg (rat, oral) 2000 mg/kg (mouse, oral) 779 mg/kg (rabbit, oral) 1700 mg/kg (rabbit, dermal) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Etridiazole is a fungicide and pesticide used for prevention of pythium ultimum on cotton plants.[2]
Synthesis
Etridiazole can be synthesised from acetonitrile as follows:
It can also be is produced by the reaction of trichloroacetamidine hydrochloride with trichloromethanesulfenyl chloride, and then with sodium hydroxide in ethanol.[3]
Reactivity
Etridiazole is stable under normal conditions,[4] but degrades upon continuous exposure to sunlight,[5] and is hydrolysed by alkalis.[6] When heated to decomposition, it emits toxic fumes of hydrogen chloride, sulfur oxides, and nitrogen oxides.[7]
Safety
Etridiazole has been classified as a Group B2 Probable Human Carcinogen.[8]
References
- ^ MacBean C, ed; e-Pesticide Manual. 15th ed., ver. 5.1, Alton, UK; British Crop Protection Council. Etridazole (2593-15-9) (2008-2010)
- ^ "Applying a Fungicide May Prevent Cotton Replanting". Ag Alert. March 27, 2002.
- ^ 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
- ^ 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
- ^ Tomlin, C.D.S. (ed.). The Pesticide Manual - World Compendium. 10th ed. Surrey, UK: The British Crop Protection Council, 1994., p. 420
- ^ 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
- ^ Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 11th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2004., p. 1623
- ^ USEPA Office of Pesticide Programs, Health Effects Division, Science Information Management Branch: "Chemicals Evaluated for Carcinogenic Potential" (April 2006)