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Bentazon

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H12N2O3S
CAS Number:
Molecular Weight:
240.28
Beilstein:
530220
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

CC(C)N1C(=O)c2ccccc2NS1(=O)=O

InChI

1S/C10H12N2O3S/c1-7(2)12-10(13)8-5-3-4-6-9(8)11-16(12,14)15/h3-7,11H,1-2H3

InChI key

ZOMSMJKLGFBRBS-UHFFFAOYSA-N

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General description

Bentazon is a commonly used pesticide which effectively controls weed in paddy fields.

Application

Bentazon has been used as analytical standard in liquid chromatograph with a photodiode array (PDA) detector coupled in series with a mass spectroscopy (MS) detector equipped with an atmospheric pressure electrospray ionization source (ESI) for the determination of bentazon and its transformation products.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Sens. 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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Certificates of Analysis (COA)

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Study of the decomposition and detoxification of the herbicide bentazon by heterogeneous photocatalysis: Kinetics, intermediates and transformation pathways.
Berberidou, Chrysanthi, et al.
Applied Catalysis. B, Environmental, 200, 150-163 (2017)
Mode of action of bentazon: Effect on photosynthesis.
Mine, Akihiko, and Shooichi Matsunaka.
Pesticide Biochemistry and Physiology, 5.5, 444-450 (1975)
Denis de la Broise et al.
Marine pollution bulletin, 64(11), 2480-2488 (2012-10-09)
Microcosms, each consisting of 2L natural surface seawater maintained in 2.3-L glass bottles, were immersed at a depth of 6m. The renewal of 10% of microcosm volumes was carried out every other day. Phytoplankton-containing seawater was used for renewal (previously
Liping Ke et al.
PloS one, 7(7), e39974-e39974 (2012-07-07)
Cotton plants engineered for resistance to the herbicides, glyphosate or glufosinate have made a considerable impact on the production of the crop worldwide. In this work, embryogenic cell cultures derived from Gossypium hirsutum L. cv Coker 312 hypocotyl callus were
Mushtaq Ahmed et al.
Bulletin of environmental contamination and toxicology, 89(2), 229-233 (2012-06-02)
The toxicological effects of the active ingredients of the herbicides diuron and bentazon on the activity of acetylcholinesterase (AChE) of krait (Bungarus sindanus) venom and electric eel (Electrophorus electricus) were studied. The diuron and entazon caused non-competitive inhibition of AChE

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