Langbahn Team – Weltmeisterschaft

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
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.050.986 Edit this at Wikidata
UNII
  • 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
  • CC(C)(C)C(=O)C(N1C=NC=N1)OC2=CC=C(C=C2)Cl
Properties
C14H16ClN3O2
Molar mass 293.75 g·mol−1
Density 1.22 g/cm3[1]
Melting point 82 °C (180 °F; 355 K)[1]
Boiling point decomposes
64 mg/L (20 °C)[1]
Hazards
Lethal dose or concentration (LD, LC):
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).

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


Quelle: https://en.wikipedia.org/wiki/Triadimefon