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Merck
CN

31596

Cycloxidim

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C17H27NO3S
CAS Number:
101205-02-1
Molecular Weight:
325.47
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753841
MDL number:
MFCD01741622
Beilstein/REAXYS Number:
8436332

Key Documents

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InChI

1S/C17H27NO3S/c1-3-6-14(18-21-4-2)17-15(19)9-13(10-16(17)20)12-7-5-8-22-11-12/h12-13,19H,3-11H2,1-2H3/b18-14+

SMILES string

CCC\C(=N/OCC)C1=C(O)CC(CC1=O)C2CCCSC2

InChI key

GGWHBJGBERXSLL-NBVRZTHBSA-N

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

storage temp.

−20°C

Quality Level

100

Related Categories

General description

Cycloxidim belongs to cyclohexanedione group and is an active selective ingredient used in herbicides.

Application

Cycloxidim has been used as working standard in the determination residual pesticides in rice using liquid chromatography-tandem mass spectrometry with electrospray ionization in positive mode (LC-MS/MS).
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

Health hazard
GHS08

signalword

Warning

hcodes

H361d

Hazard Classifications

Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCK1410
BCBZ4184
BCBW0525

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Determination of twenty pesticides in rice by employing QuEChERS and LC-ESI-MS/MS.
Rebelo, Andrey M., et al.
Analytical Methods : Advancing Methods and Applications, 6.23, 9469-9476 (2014)
The effect of cycloxydim tolerant maize (CTM) alleles on grain yield and agronomic traits of maize single cross hybrid.
Vancetovic, J., et al.
Maydica, 54.1 , 91-91 (2009)
Shirin Monadjemi et al.
Chemosphere, 89(3), 269-273 (2012-05-19)
The reactivity of the herbicide cycloxydim (CD) toward singlet oxygen was studied in organic solution and on wax films to mimic the leaf surface. Experiments in solution were conducted in acetonitrile using phenalenone as a sensitizer. For the experiments in
K M Cocker et al.
Pest management science, 57(7), 587-597 (2001-07-24)
Herbicide-resistant Lolium multiflorum (Italian rye-grass) was first reported in the UK in 1993 and had been confirmed on 25 farms by 1999. In this study, resistance to five herbicides belonging to the aryloxyphenoxypropionate, cyclohexanedione and phenyl-urea classes was determined in
Cafer Turgut
Environmental science and pollution research international, 12(6), 342-346 (2005-11-25)
Aquatic plants have a great potential to function as in situ, on-site biosinks and biofilters of pollutants. They are used for phytoremediation and phytotoxicity studies. Pesticide uptake studies are very important to predict contaminant accumulation, translocation, and transformation. There are
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