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Methabenzthiazuron

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C10H11N3OS
CAS Number:
Molecular Weight:
221.28
Beilstein:
196633
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

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)

InChI key

RRVIAQKBTUQODI-UHFFFAOYSA-N

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General description

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′.

Application

Methabenzthiazuron may be used as an analytical reference standard for the determination of the analyte in drinking water, soil and fruits 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.

Legal Information

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

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

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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Determination of phenylurea herbicides in drinking water.
Hamada M and Wintersteiger R
J. Planar Chromatogr., 15(1), 11-18 (2002)
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)
Moulay A Malouki et al.
Chemosphere, 60(11), 1523-1529 (2005-08-09)
The influence of nitrate and nitrite ions on the degradation of methabenzthiazuron upon irradiation using artificial solar light has been investigated. The rate of degradation of methabenzthiazuron (1 microM) was accelerated by NO3- (0.1 mM) by a factor of 10.
Moulay Abderrahmane Malouki et al.
Environmental toxicology and chemistry, 22(9), 2013-2019 (2003-09-10)
We investigated the transformation of methabenzthiazuron in water by microorganisms and solar light. This compound was very slowly phototransformed when irradiated at lambda > 290 nm, but it could be successfully oxidized into 6-hydroxymethabenzthiazuron by Aspergillus niger, as shown by
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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