Triadimefon

Triadimefon
Names
	IUPAC name 1-(4-Chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one
	Other names Triadimeform
Identifiers
CAS Number	43121-43-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:9665 ;
ChemSpider	36029;
ECHA InfoCard	100.050.986
PubChem CID	39385;
UNII	1HW039CJF0 ;
CompTox Dashboard (EPA)	DTXSID3023897 ;
	InChI InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3 Key: WURBVZBTWMNKQT-UHFFFAOYSA-N; InChI=1/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3 Key: WURBVZBTWMNKQT-UHFFFAOYAV;
	SMILES CC(C)(C)C(=O)C(N1C=NC=N1)OC2=CC=C(C=C2)Cl;
Properties
Chemical formula	C14H16ClN3O2
Molar mass	293.75 g·mol−1
Density	1.22 g/cm3
Melting point	82 °C (180 °F; 355 K)
Boiling point	decomposes
Solubility in water	64 mg/L (20 °C)
Hazards
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	363 mg/kg (oral, rat); > 5000 mg/kg (dermal, rat)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Triadimefon is a fungicide used in agriculture to control various fungal diseases. As a seed treatment, it is used on barley, corn, cotton, oats, rye, sorghum, and wheat.^[2] In fruit it is used on pineapple and banana.^[2] Non-food uses include pine seedlings, Christmas trees, turf, ornamental plants, and landscaping.^[2]

References

^ ^a ^b ^c ^d ^e Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
^ ^a ^b ^c "Triadimefon Reregistration Eligibility Decision (RED) and Triadimenol Tolerance Reassessment and Risk Management Decision (TRED) Fact Sheet". Environmental Protection Agency.

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[GESTIS-1] Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health

[EPA-2] "Triadimefon Reregistration Eligibility Decision (RED) and Triadimenol Tolerance Reassessment and Risk Management Decision (TRED) Fact Sheet". Environmental Protection Agency.

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[2]