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 (Jmol)	Interactive image
ChEBI	CHEBI:9665
ChemSpider	36029
ECHA InfoCard	100.050.986
PubChem	39385
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/cm^3[1]
Melting point	82 °C (180 °F; 355 K) [1]
Boiling point	decomposes
Solubility in water	64 mg/L (20 °C)[1]
Hazards
Lethal dose or concentration (LD, LC):
LD50 (median dose)	363 mg/kg (oral, rat)[1] > 5000 mg/kg (dermal, rat)[1]
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

1. Record in the GESTIS Substance Database of the IFA
2. "Triadimefon Reregistration Eligibility Decision (RED) and Triadimenol Tolerance Reassessment and Risk Management Decision (TRED) Fact Sheet". Environmental Protection Agency.