Dimefox
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Dimefox | |||||||||||||||
other names |
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Molecular formula | C 4 H 12 FN 2 OP | |||||||||||||||
Brief description |
colorless liquid with a fishy odor |
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properties | ||||||||||||||||
Molar mass | 154.12 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
1.1151 g cm −3 |
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boiling point |
85 ° C (20 hPa) |
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Vapor pressure |
0.14 mbar (20 ° C) |
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solubility |
miscible with water and most organic solvents |
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Refractive index |
1.4266 |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
Dimefox is a chemical compound from the group of organic fluorine compounds and phosphoric acid amides .
Extraction and presentation
Dimefox can be obtained by fluorinating bis (dimethylamido) phosphoryl chloride.
properties
Dimefox is a colorless liquid with a fishy odor that can be mixed with water. It acts as an inhibitor of acetylcholinesterase .
use
Like the related compounds Schradan , Mazidox and Mipafox , Dimefox , which came on the market in 1940, is used as an insecticide . Dimefox was used against plant lice and spider mites , among other things . The active ingredient is absorbed and stored by the plant, where it remains effective for a long time.
However, it is classified as obsolete by the World Health Organization and is rarely used worldwide.
Admission
In the European Union, Dimefox is not included in Annex I of Directive 91/414 / EEC with Regulation (EC) No. 2076/2002 of November 20, 2002, so the active ingredient is no longer a plant protection product in the EU countries authorized. In Switzerland, too, no pesticides containing this active ingredient are permitted.
Individual evidence
- ↑ a b c d e f g h Entry on Dimefox in the GESTIS substance database of the IFA , accessed on January 8, 2018(JavaScript required) .
- ↑ a b c Entry on Dimefox in the Hazardous Substances Data Bank , accessed July 29, 2012.
- ↑ Nikitin, EV; Ignat'ev, Yu. A .; Romakhin, AS; Parakin, OV; Kosachev, IP; et al .: Anodic fluorination of phosphorodiamidites and phosphorous triamides . In: Journal of general chemistry of the USSR . tape 52 , no. 12 , 1982, ISSN 0022-1279 , pp. 2792-2793 .
- ↑ Entry on Dimefox in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on February 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
- ↑ a b Entry on Dimefox in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on December 30, 2011.
- ^ Robert Irving Krieger, Handbook of Pesticide Toxicology: Principles. ISBN 978-0-1242-6260-7 , p. 914.
- ↑ World Health Organization: The WHO recommended classification of pesticides by hazard and guidelines to classification: 2009 . Wissenschaftliche Verlagsgesellschaft mbH, 2009, ISBN 978-92-4154796-3 , ISSN 1684-1042 ( who.int [PDF]).
- ↑ Regulation (EC) No. 2076/2002 (PDF) of the Commission of November 20, 2002
- ↑ General Directorate Health and Food Safety of the European Commission: Entry on Dimefox in the EU pesticide database; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on March 26, 2016.