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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
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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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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary 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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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)
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
Palash Kumar Das et al.
Protoplasma, 249(1), 65-74 (2011-01-27)
In this article, we describe the modifications in the antioxidant system of Synechococcus elongatus PCC7942 mutant Mu2 capable of growing at five times higher concentration of bentazone than wild type. Nevertheless, in both the strains, bentazone almost identically induced light-dependent
Mohamed A Balah et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(5), 390-396 (2012-03-20)
Efficiency of different tank-mixed additives with bentazon at half rate was investigated on (Malva parviflora) and other broad leaf weeds compared with bentazon at the full recommended rate without additives in peas in open field. All the tested additives enhanced
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