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36156

Supelco

Methabenzthiazuron

PESTANAL®, analytical standard

Sinonimo/i:

1-(Benzothiazol-2-yl)-1,3-dimethylurea

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About This Item

Formula empirica (notazione di Hill):
C10H11N3OS
Numero CAS:
Peso molecolare:
221.28
Beilstein:
196633
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
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

CNC(=O)N(C)c1nc2ccccc2s1

InChI

1S/C10H11N3OS/c1-11-9(14)13(2)10-12-7-5-3-4-6-8(7)15-10/h3-6H,1-2H3,(H,11,14)
RRVIAQKBTUQODI-UHFFFAOYSA-N

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Descrizione generale

Methabenzthiazuron is commonly used to control weeds and grasses, particularly in cereals, legumes and maize fields. It is regarded as very toxic for the environment and aquatic organisms. Mode of action of the herbicide involves inhibition of the ′Hill reaction′.[1][2]

Applicazioni

Methabenzthiazuron may be used as an analytical reference standard for the determination of the analyte in drinking water,[3] soil[4] and fruits[5] using various chromatography techniques.
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, Faceshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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The influence of the herbicide methabenzthiazuron on the synthesis of plastidic lipids in Hordeum vulgare seedlings.
Kleudgen HK
Pesticide Biochemistry and Physiology, 9(1), 57-60 (1978)
Methabenzthiazuron degradation with illuminated TiO2 aqueous suspensions. Kinetic and reactional pathway investigations.
Mezioud N, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 288, 13-22 (2014)
Florence Lagarde et al.
Journal of agricultural and food chemistry, 54(20), 7450-7459 (2006-09-28)
An analytical method has been developed for the quantification of two herbicides (ethidimuron and methabenzthiazuron) and their two main soil derivatives. This method involves fluidized-bed extraction (FBE) prior to cleanup and analysis by reverse-phase liquid chromatography with UV detection at
How to overcome matrix effects in the determination of pesticides in fruit by HPLC ESI MS MS.
Bester K, et al.
Fresenius Journal of Analytical Chemistry, 371(4), 550-555 (2001)
H P Malkomes
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes, 134(7), 573-586 (1979-01-01)
In a field experiment the herbicides U 46 PD-Fluid (dichlorprop salt) and Tribunil (methabenzthiazuron) were applied in April 1976 post-emergence to winter wheat cultivated in 3 different soils. After 4 days, 1, 2 and 3 months samples were taken from

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