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45693

Supelco

Triadimefon

PESTANAL®, analytical standard

Synonym(s):

1-(4-Chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanone

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About This Item

Empirical Formula (Hill Notation):
C14H16ClN3O2
CAS Number:
43121-43-3
Molecular Weight:
293.75
Beilstein:
619231
EC Number:
256-103-8
MDL number:
MFCD00055506
UNSPSC Code:
41116107
PubChem Substance ID:
329756906
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2cncn2

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

InChI key

WURBVZBTWMNKQT-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H302 - H317 - H330 - H410

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Skin Sens. 1

Storage Class Code

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF2519
BCBW0134
BCBT6245
BCBT9575
SZBD071XV

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Jones A Kapeleka et al.
PloS one, 15(7), e0235345-e0235345 (2020-07-16)
This study was carried out to investigate the risks of simultaneous exposure to pesticide residues and bacteria contaminants in locally produced fresh vegetables and vegetables in Tanzania. A total of 613 samples were analyzed for pesticide residues, out of which
Galina V Kokurkina et al.
European journal of medicinal chemistry, 46(9), 4374-4382 (2011-08-02)
A series of 2-arylhydroxynitroindoles were prepared and tested for antifungal activity in vitro. The preliminary bioassays indicated that some compounds are comparable to the commercial fungicide (triadimefon). To further explore the structure-activity relationships, the data set of the seventeen structures
Xin Liu et al.
Fungal genetics and biology : FG & B, 48(2), 113-123 (2010-10-20)
Analysis of the genome sequence of Fusarium graminearum revealed three paralogous cyp51 genes (designated cyp51A, -B, and -C) encoding 14-α demethylases in this fungus. Targeted gene disruption showed that the cyp51A, -B or -C disruption mutants were morphologically indistinguishable from
Arthur W Garrison et al.
Environmental science & technology, 45(6), 2186-2193 (2011-02-24)
The microbial transformation of triadimefon, an agricultural fungicide of the 1,2,4-triazole class, was followed at a nominal concentration of 50 μg/mL over 4 months under aerobic conditions in three different soil types. Rates and products of transformation were measured, as
Zhaoyang Li et al.
Environmental science & technology, 45(7), 2797-2803 (2011-03-12)
Triadimefon is a widely used triazole fungicide with one chiral carbon center. In soils, plants, and animals, triadimefon could be metabolized to triadimenol by reduction of the carbonyl group to an alcohol, resulting in the occurrence of a second chiral
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