Orysastrobin

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Structural formula
Structural formula of orysastrobin
General
Surname Orysastrobin
other names

(2 E ) -2- (methoxyimino) -2- {2 - [(3 E , 5 E , 6 E ) -5- (methoxyimino) -4,6-dimethyl-2,8-dioxa-3,7- diazanona-3,6-dien-1-yl] phenyl} - N -methylacetamide

Molecular formula C 18 H 25 N 5 O 5
Brief description

white to yellowish solid with a slightly aromatic odor

External identifiers / databases
CAS number 248593-16-0
EC number 607-448-1
ECHA InfoCard 100.121.438
PubChem 11486133
Wikidata Q19297703
properties
Molar mass 391.42 g mol −1
Physical state

firmly

Melting point

96-100 ° C

boiling point

225 ° C (decomposition)

solubility
  • practically insoluble in water (80 mg l −1 at 20 ° C)
  • Easily soluble in ethyl acetate and toluene
safety instructions
GHS labeling of hazardous substances
07 - Warning 08 - Dangerous to health 09 - Dangerous for the environment

Caution

H and P phrases H: 302-332-351-410
P: 273-281-501
Toxicological data
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Orysastrobin is a chemical compound from the group of amides and methoxyiminoacetamide - strobilurins .

properties

Orysastrobin is a white to yellowish solid with a slightly aromatic odor that is practically insoluble in water.

use

Orysastrobin is used as a fungicide . It is a systemic fungicide with curative and protective properties and a broad spectrum of activity. It disrupts the respiratory processes of the mushrooms (QoI fungicide - Quinone outside inhibitors). It was presented by BASF in 2004, launched in 2007 and marketed against fungal diseases in rice.

Plant protection products containing this active ingredient are not permitted in any EU country or in Switzerland .

Individual evidence

  1. a b c d e f g h i j data sheet Orysastrobin at Sigma-Aldrich , accessed on May 21, 2017 ( PDF ).
  2. a b Entry on orysastrobin in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on January 28, 2015.
  3. Ulrich Schirmer, Peter Jeschke, Matthias Witschel: Modern Crop Protection Compounds: Herbicides . John Wiley & Sons, 2012, ISBN 978-3-527-32965-6 , pp. 586,616 ( limited preview in Google Book Search).
  4. ^ Directorate-General for Health and Food Safety of the European Commission: Entry on orysastrobin in the EU pesticide database; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on February 14, 2016.