Dichlofluanid
Names | |
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IUPAC name
N-{[Dichloro(fluoro)methyl]sulfanyl}-N′,N′-dimethyl-N-phenylsulfuric diamide | |
Identifiers | |
1085-98-9 | |
3D model (Jmol) | Interactive image |
ChemSpider | 13520 |
ECHA InfoCard | 100.012.835 |
PubChem | 14145 |
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Properties | |
C9H11Cl2FN2O2S2 | |
Molar mass | 333.22 g·mol−1 |
Density | 1,55 g/cm3 |
Melting point | 105-106 °C |
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 scab, 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.
References
- ↑ 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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