Dichlofluanid
 | |
| Names | |
|---|---|
| IUPAC name
N-{[Dichloro(fluoro)methyl]sulfanyl}-N′,N′-dimethyl-N-phenylsulfuric diamide | |
| Identifiers | |
| 3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.012.835 |
| PubChem CID |
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| Properties | |
| C9H11Cl2FN2O2S2 | |
| Molar mass | 333.22 g·mol−1 |
| Density | 1,55 g/cm3 |
| Melting point | 105-106 °C |
| Hazards | |
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) |
2500 mg/kg (rat)[1] |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Dichlofluanid (N-dichlorofluoromethylthio-N′, N′-dimethyl-N-phenylsulfamide) is a fungicide used to protect strawberries, grapes, berries, apples, pears and other fruit, vegetables and ornamental plants from diseases such as apple scab (Venturia inaequalis),[2] black spot, leather rot, gray mold, downy mildew and others caused by the fungi Botrytis, Alternaria, Sclerotinia, and Monilinia. It is also used to protect against diseases of fruit during storage, and as a wood preservative, often as part of a paint undercoat.[3]
Dichlofluanid was first marketed by Bayer Company in 1964, for use as a fungicide on plants.[3] Its trade names include Euparen and Elvaron.[1]
References
- 1 2 Zhou, X; Cao, S; Li, X; Xi, C; Ding, X; Xu, F; Hu, J; Chen, Z (2016). "Rapid Determination of Dichlofluanid Residues in Vegetables Using Dispersive-SPE Sample Preparation Combined with Gas Chromatography-Mass Spectrometry". Journal of chromatographic science. 54 (5): 858–63. PMC 4890451
. PMID 26921896. doi:10.1093/chromsci/bmw006. - ↑ Matolcsy, György; Nádasy, Miklós; Andriska, Viktor, eds. (1988). "5. Fungicides". Studies in Environmental Science: Volume 32 Pesticide chemistry. Amsterdam: Elsevier. p. 341. ISBN 978-0-444-98903-1.
- 1 2 Unger, A; Schniewind, AP; Unger, W (2001). "7.3.9.1.: Dichlofluanid (N-Dichlorofluoromethylthio-N'-N'-dimethyl-N-phenylsulfamide)". Conservation of Wood Artifacts: A Handbook. Berlin, Heidelberg: Springer Berlin Heidelberg. pp. 217–218. ISBN 9783662063989.
- Rocket NXT
- Monitoring of the booster biocide dichlofluanid ... [Chemosphere. 2005] - PubMed - NCBI
- Dichlofluanid toxicity reports, review - hazard potential, risk
- GC determination of dichlofluanid (Euparen) residues and its metabolite dimethylphenylsulfamide (DMSA) in strawberries - Springer
- Directive 98/8/EC concerning the placing of biocidal products on the market, Assessment Report Dichlofluanid
- PAN Pesticides Database - Chemicals: N,N-Dimethylsulfamide (metabolite of tolylfluanid).
- Ham, N.S.: Dichlorofluoromethanesulfenyl chloride in J. Am. Chem. Soc. 83 (1961) 751–752, doi:10.1021/ja01464a052.
- T.R. Roberts, D.H. Hutson, Metabolic Pathways of agrochemicals. Part one: Herbicides and Plant Growth Regulators, Royal Society of Chemistry Publishers, London (1998)
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