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Merck
CN

45442

Diclofop-methyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H14Cl2O4
CAS Number:
51338-27-3
Molecular Weight:
341.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756737
EC Number:
257-141-8
Beilstein/REAXYS Number:
2224754
MDL number:
MFCD00128052

Key Documents

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InChI key

BACHBFVBHLGWSL-UHFFFAOYSA-N

InChI

1S/C16H14Cl2O4/c1-10(16(19)20-2)21-12-4-6-13(7-5-12)22-15-8-3-11(17)9-14(15)18/h3-10H,1-2H3

SMILES string

COC(=O)C(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

42-48 °C (if solid)

application(s)

agriculture
environmental

format

neat

Quality Level

100

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General description

Diclofop-methyl is an early post-emergence phenoxypropanoic acid herbicide. Its mode of action involves inhibition of acetyl CoA carboxylase (ACCase) activity, which in turn decreases fatty acid synthesis in weeds and inhibits photosynthesis and the activity of meristem.

Application

Diclofop-methyl may be used as a reference standard for the determination of diclofop-methyl in soil samples by gas-liquid chromatography (GLC).
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

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - 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
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH5172
BCBZ5051
BCBT3269

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Q Yu et al.
Plant, cell & environment, 36(4), 818-827 (2012-10-11)
Lolium rigidum is an obligately cross-pollinated, genetically diverse species and an economically important herbicide resistance-prone weed. Our previous work has demonstrated that recurrent selection of initially susceptible L. rigidum populations with low herbicide rates results in rapid herbicide resistance evolution.
Xiyun Cai et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 41(7), 1115-1129 (2006-08-23)
Cyclodextrins (CDs) possess a hydrophilic external surface and a hydrophobic cavity. They are thus highly soluble and, in the meantime, effectively form inclusion complexes with hydrophobic organic compounds to enhance their solubilities. In this study, the complexation between modified beta-CDs
Danuta Palut et al.
Roczniki Panstwowego Zakladu Higieny, 53(1), 1-9 (2002-06-11)
The study was designed to determine whether diclofop, introduced to environment as herbicide, would exert properties of chemical inducers of rat liver monooxygenase system related to CYP1A and CYP2B isozymes. For this purpose, the effect of diclofop on 7-etoxyresorufin O-dealkylase
Xi-yun Cai et al.
Journal of environmental sciences (China), 17(1), 67-71 (2005-05-20)
Hydrolytic degradation of the herbicide diclofop-methyl was investigated in the multi-pH deionized water, natural aquatic systems and soil suspensions. Resulting data indicated that the herbicide was stable in the acidic and nearly neutral solutions for at least 15 d. The
Peter J Holloway et al.
Pest management science, 59(11), 1237-1244 (2003-11-19)
Although it is well known that judicious use of adjuvants can increase the performance of foliage-applied sprays of many agrochemicals, little information is available in the public domain about their ultimate effects on pesticide residues in treated crops. In the
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