Skip to Content
Merck
CN

32052

Bentazon

PESTANAL®, analytical standard

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C10H12N2O3S
CAS Number:
25057-89-0
Molecular Weight:
240.28
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753982
EC Number:
246-585-8
Beilstein/REAXYS Number:
530220
MDL number:
MFCD00078640

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Bentazon, PESTANAL®, analytical standard

InChI key

ZOMSMJKLGFBRBS-UHFFFAOYSA-N

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

SMILES string

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

grade

analytical standard

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

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

General description

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

Other Notes

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

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM5259
BCCL8155
BCCC5313
BCBZ3560

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service