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Key Documents

34232

Supelco

Prothioconazole

PESTANAL®, analytical standard

Sinonimo/i:

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

Formula empirica (notazione di Hill):
C14H15Cl2N3OS
Numero CAS:
Peso molecolare:
344.26
Codice UNSPSC:
41116107
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
MNHVNIJQQRJYDH-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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

Note legali

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

Pittogrammi

Environment

Avvertenze

Warning

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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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
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
Hyunkyu Sang et al.
Frontiers in microbiology, 9, 2335-2335 (2018-10-18)
The succinate dehydrogenase inhibitor (SDHI) fungicide, fluopyram, is used as a soybean seed treatment to manage Fusarium virguliforme, the casual agent of sudden death syndrome (SDS). More recently, other species within clade 2 of the Fusarium solani species, F. tucumaniae

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