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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
Yepeng Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 1012-1019 (2012-09-05)
The binding mechanism of triadimenol (NOL) to calf thymus DNA (ctDNA) in physiological buffer (pH 7.4) was investigated by multispectroscopic methods including UV-vis absorption, fluorescence, circular dichroism (CD), Fourier transform infrared (FT-IR), and nuclear magnetic resonance ((1)H NMR) spectroscopy, coupled
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
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
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