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Merck
CN

34232

Prothioconazole

PESTANAL®, analytical standard

Synonym(s):

2-[2-(1-Chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-3H-1,2,4-triazole-3-thione

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About This Item

Empirical Formula (Hill Notation):
C14H15Cl2N3OS
CAS Number:
Molecular Weight:
344.26
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24
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Product Name

Prothioconazole, PESTANAL®, analytical standard

SMILES string

OC(CN1N=CNC1=S)(Cc2ccccc2Cl)C3(Cl)CC3

InChI

1S/C14H15Cl2N3OS/c15-11-4-2-1-3-10(11)7-14(20,13(16)5-6-13)8-19-12(21)17-9-18-19/h1-4,9,20H,5-8H2,(H,17,18,21)

InChI key

MNHVNIJQQRJYDH-UHFFFAOYSA-N

grade

analytical standard

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

Quality Level

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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.

General description

Prothioconazole is a triazolinethione derivative, which can be used as a fungicide in order to inhibit the activity of demethylase enzyme.(1) It can be used in the treatment of infection in crops like wheat, caused by Mycosphaerella graminicola, a plant-pathogenic fungus.

Legal Information

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

农药列管产品
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Mechanism of binding of prothioconazole to Mycosphaerella graminicola CYP51 differs from that of other azole antifungals
Parker.EJ, et al.
Applied and Environmental Microbiology, 77, 1460-1465 (2011)
Joel D A Tyndall et al.
PloS one, 11(12), e0167485-e0167485 (2016-12-03)
Azole antifungals, known as demethylase inhibitors (DMIs), target sterol 14α-demethylase (CYP51) in the ergosterol biosynthetic pathway of fungal pathogens of both plants and humans. DMIs remain the treatment of choice in crop protection against a wide range of fungal phytopathogens
Carsten Albrecht Brühl et al.
Environmental science and pollution research international, 18(1), 31-37 (2010-06-15)
Seed treatments are widely used on cereals and other annual crops throughout Europe. Most of the formulated pesticide is found on the outside of the seed, the husk. Risk assessments of seed treatments are especially needed for granivorous mice living
Zhaoxian Zhang et al.
Journal of agricultural and food chemistry, 65(37), 8241-8247 (2017-08-29)
An efficient and sensitive chiral analytical method was established for the determination of the chiral fungicide prothioconazole and its major chiral metabolite prothioconazole-desthio in agricultural and environmental samples using ultraperformance liquid chromatography-tandem mass spectrometry. The optical rotation and absolute configuration
Parvaneh Balsini et al.
Journal of separation science, 42(23), 3553-3562 (2019-10-05)
In this study, QuEChERS combined with dispersive liquid-liquid microextraction is developed for extraction of ten pesticides in complex sample matrices of water and milk. In this regard, effective factors of proposed extraction technique combined with gas chromatography with flame ionization

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