Fluazinam

Fluazinam
Names
	IUPAC name 3-Chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-2-pyridinamine
Identifiers
CAS Number	79622-59-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:81843 ;
ChemSpider	82831;
ECHA InfoCard	100.114.073
PubChem CID	91731;
UNII	0P91PCK33Q ;
CompTox Dashboard (EPA)	DTXSID7032551 ;
	InChI InChI=1S/C13H4Cl2F6N4O4/c14-6-1-4(12(16,17)18)3-22-11(6)23-9-7(24(26)27)2-5(13(19,20)21)8(15)10(9)25(28)29/h1-3H,(H,22,23) Key: UZCGKGPEKUCDTF-UHFFFAOYSA-N; InChI=1/C13H4Cl2F6N4O4/c14-6-1-4(12(16,17)18)3-22-11(6)23-9-7(24(26)27)2-5(13(19,20)21)8(15)10(9)25(28)29/h1-3H,(H,22,23) Key: UZCGKGPEKUCDTF-UHFFFAOYAY;
	SMILES C1=C(C=NC(=C1Cl)NC2=C(C=C(C(=C2[N+](=O)[O-])Cl)C(F)(F)F)[N+](=O)[O-])C(F)(F)F;
Properties
Chemical formula	C13H4Cl2F6N4O4
Molar mass	465.09 g·mol−1
Density	1.8±0.1 g/cm3
Melting point	116 °C (241 °F; 389 K)
Boiling point	376.1±42.0°C (Predicted)
Solubility in water	1.76 mg/L
Vapor pressure	5.51×10-8 mmHg (Predicted)
Hazards
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	5000mg/kg (rat, oral); 4190mg/kg (mallard, oral); ≥200μg (bee, contact); ≥1000mg/kg (worm, 28 day)
LC50 (median concentration)	61ppb (rainbow trout, 96h)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Fluazinam is a broad-spectrum fungicide used in agriculture. It is classed as a diarylamine and more specifically an arylaminopyridine. Its chemical name is 3-chloro-N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-2-pyridinamine.[1] The mode of action involves the compound being an extremely potent uncoupler of oxidative phosphorylation in mitochondria[2] and also having high reactivity with thiols.[1] It is unique amongst uncouplers in displaying broad-spectrum activity against fungi and also very low toxicity to mammals due to it being rapidly metabolised to a compound without uncoupling activity.[1][3] It was first described in 1992 and was developed by researchers at the Japanese company Ishihara Sangyo Kaisha.[4]

Uses

Fluazinam is a protectant fungicide, but is neither systemic or curative. It acts by inhibiting the germination of spores and the development of infection structures. Although it has activity against many fungi, it is less potent against rusts and powdery mildew and as such has not been commercialised for use in cereal crops. It is widely used to control late blight (P. infestans) in potato due to its activity against the zoospores of the pathogen which makes it particularly effective at controlling infection of the potato tubers. Despite its common usage to control late blight, there are no reports of resistance to fluazinam appearing in P. infestans. Fluazinam is also used to control Sclerotinia on peanuts and turf, Botrytis on grapes and beans and clubroot in brassicas.[1]

Toxicity

The acute oral median lethal dose in rats is very low at over 5000 mg/kg due to the compound's reactivity with thiols. This reactivity can have negative consequences since repeated exposure can cause skin sensitization and dermatitis to develop in some individuals. Fluazinam also displays low toxicity to birds, bees and worms, but has a high toxicity to fish. The toxicity towards fish is considered to be relatively unimportant, since the compound has a very short half-life (around 1 day) in aquatic systems.[1]

gollark: * i.e. you can pick multiple

gollark: > @a russian spy I agree; but what voting system do you suggest for Esolangs dictatorial elections?... approval voting, basically what we do now but with multiple candidates.

gollark: ++DELETE <@!309787486278909952>

gollark: And? That is not an argument for plurality voting.

gollark: Bees WILL be dispatched toward anyone who glorifies plurality voting/first past the post.

References

Ulrich Schirmer; Peter Jeschke; Matthias Witschel (2012). Modern Crop Protection Compounds: Herbicides. John Wiley & Sons. pp. 662–663. ISBN 978-3-527-32965-6.
Ze-jian Guo, Hideto Miyoshi, Terumasa Komyoji, Takahiro Haga, Toshio Fujita (1991). "Uncoupling activity of a newly developed fungicide, fluazinam [3-chloro-N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-2-pyridinamine]". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1056 (1): 89–92. doi:10.1016/S0005-2728(05)80077-5.CS1 maint: uses authors parameter (link)
Society for General Microbiology. Symposium (4 May 1995). Fifty Years of Antimicrobials: Past Perspectives and Future Trends. Cambridge University Press. pp. 104–105. ISBN 978-0-521-48108-3.
Robert Krieger (17 October 2001). Handbook of Pesticide Toxicology, Two-Volume Set: Principles and Agents. Academic Press. p. 1243. ISBN 978-0-08-053379-7.

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[SchirmerJeschke2012-1] Ulrich Schirmer; Peter Jeschke; Matthias Witschel (2012). Modern Crop Protection Compounds: Herbicides. John Wiley & Sons. pp. 662–663. ISBN 978-3-527-32965-6.

[2] Ze-jian Guo, Hideto Miyoshi, Terumasa Komyoji, Takahiro Haga, Toshio Fujita (1991). "Uncoupling activity of a newly developed fungicide, fluazinam [3-chloro-N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-2-pyridinamine]". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1056 (1): 89–92. doi:10.1016/S0005-2728(05)80077-5.CS1 maint: uses authors parameter (link)

[Symposium1995-3] Society for General Microbiology. Symposium (4 May 1995). Fifty Years of Antimicrobials: Past Perspectives and Future Trends. Cambridge University Press. pp. 104–105. ISBN 978-0-521-48108-3.

[Krieger2001-4] Robert Krieger (17 October 2001). Handbook of Pesticide Toxicology, Two-Volume Set: Principles and Agents. Academic Press. p. 1243. ISBN 978-0-08-053379-7.