Fluazolate

Structural formula
General
Surname	Fluazolate
other names	Isopropyl 5- [4-bromo-1-methyl-5- (trifluoromethyl) pyrazol-3-yl] -2-chloro-4-fluorobenzoate ( IUPAC ); 1-Methylethyl 5- [4-bromo-1-methyl-5- (trifluoromethyl) -1 H -pyrazol-3-yl] -2-chloro-4-fluorobenzoate;
Molecular formula	C 15 H 12 BrClF 4 N 2 O 2
Brief description	colorless solid
External identifiers / databases
PubChem	3083545
Wikidata	Q1430444
properties
Molar mass	443.62 g mol −1
Physical state	firmly
density	1.62 g cm −3 (bulk density)
Melting point	80 ° C
solubility	practically insoluble in water
safety instructions
GHS labeling of hazardous substances	no GHS pictograms
	no GHS pictograms
H and P phrases	H: no H-phrases
	P: no P-phrases
Toxicological data	5000 mg kg −1 ( LD 50 , rat , oral )
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Fluazolate is a chemical compound from the group of phenylpyrazoles .

properties

Fluazolate is a colorless solid that is practically insoluble in water. It is structurally related to pyraflufen-ethyl and was developed by Monsanto .

use

Fluazolate is used as a herbicide . The effect is based on the inhibition of photosynthesis .

Admission

The approval of the active ingredient for the European Union was granted in 1997 by Twinagro Ltd. requested. The Commission initially assessed the documents as complete and, with Decision 98/676 / EC, granted the provisional authorization of plant protection products containing fluazolate. However, pesticides containing fluazolate have not been approved in any country of the Union. Gaps were later identified in the application documents that the applicant could not or did not want to fix. The Commission withdrew the possibility of provisional approval in 2002.

In Germany, Austria and Switzerland, no pesticides with the active ingredient fluazolate are permitted.

Individual evidence

↑ ^a ^b ^c ^d ^e ^f ^g ^h Entry on fluazolate in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on August 1, 2013.
↑ ^a ^b clearsynth: Fluazolate , accessed on May 6, 2017.
↑ Wolfgang Krämer, Ulrich Schirmer, Peter Jeschke, Matthias Witschel: Modern Crop Protection Compounds . John Wiley & Sons, 2012, ISBN 978-3-527-32965-6 , pp. 168 ( limited preview in Google Book search).
↑ Decision of the Commission of September 10, 2002 amending Decision 98/676 / EC with regard to fluazolate (PDF)
↑ General Directorate Health and Food Safety of the European Commission: Entry on Fluazolate (formerly isopropozole) in the EU pesticide database ; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on February 24, 2016.

[PPDB-1] ↑ ^a ^b ^c ^d ^e ^f ^g ^h Entry on fluazolate in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on August 1, 2013.

[clearsynth-2] rsynth: Fluazolate , accessed on May 6, 2017.

[Wolfgang_Krämer,_Ulrich_Schirmer,_Peter_Jeschke,_Matthias_Witschel-3] Wolfgang Krämer, Ulrich Schirmer, Peter Jeschke, Matthias Witschel: Modern Crop Protection Compounds . John Wiley & Sons, 2012, ISBN 978-3-527-32965-6 , pp. 168 ( limited preview in Google Book search).

[4] Decision of the Commission of September 10, 2002 amending Decision 98/676 / EC with regard to fluazolate (PDF)

[PSM-5] General Directorate Health and Food Safety of the European Commission: Entry on Fluazolate (formerly isopropozole) in the EU pesticide database ; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on February 24, 2016.