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Merck
CN

45442

Supelco

Diclofop-methyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H14Cl2O4
CAS Number:
Molecular Weight:
341.19
Beilstein:
2224754
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

mp

42-48 °C (if solid)

application(s)

agriculture
environmental

format

neat

SMILES string

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

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

InChI key

BACHBFVBHLGWSL-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - 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

Regulatory Information

农药列管产品
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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
Haifeng Qian et al.
Journal of agricultural and food chemistry, 60(22), 5515-5523 (2012-05-23)
Diclofop methyl (DM) is a chiral herbicide that is widely used as a racemic mixture. This study analyzed the enantioselective effects of R- and S-DM on rice at the physiological and molecular levels. DM exerts an enantioselective effect on rice
Diclofop-methyl affects microbial rhizosphere community and induces systemic acquired resistance in rice.
Chen S, et al.
Journal of environmental sciences (China), 51, 352-360 (2017)
Determination of diclofop-methyl and diclofop in soil by gas-liquid chromatography of their pentafluorobenzyl esters.
Gaynor, John D and MacTavish, Donald C
Analyst, 107(1275), 700-703 (1982)
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

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