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Merck
CN

35031

Oxyfluorfen

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H11ClF3NO4
CAS Number:
42874-03-3
Molecular Weight:
361.70
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755114
EC Number:
255-983-0
Beilstein/REAXYS Number:
2065259
MDL number:
MFCD00072435

Key Documents

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InChI key

OQMBBFQZGJFLBU-UHFFFAOYSA-N

InChI

1S/C15H11ClF3NO4/c1-2-23-14-8-10(4-5-12(14)20(21)22)24-13-6-3-9(7-11(13)16)15(17,18)19/h3-8H,2H2,1H3

SMILES string

CCOc1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([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

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General description

Oxyfluorfen is a diphenyl-ether herbicide, which can be commonly used in vineyards for weed control management. It can block the chlorophyll biosynthesis in plants by inhibiting protoporphyrinogen oxidase enzyme

Application

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

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH2937
BCBW2993

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Photochemical behaviour of oxyfluorfen: a diphenyl-ether herbicide
Scrano L, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 129, 65-70 (1999)
Effect of oxyfluorfen and diuron alone and in mixture on antioxidative enzymes of Scenedesmus obliquus
Geoffroy L, et al.
Pesticide Biochemistry and Physiology, 72, 178-185 (2002)
Jui-Hung Yen et al.
Ecotoxicology and environmental safety, 54(2), 151-156 (2003-01-29)
The dissipation and mobility of the herbicide oxyfluorfen (2-chloro-alpha,alpha,alpha-trifluoro-p-tolyl 3-ethoxy-4-nitrophenyl ether) in field soil of Taiwan were investigated in the laboratory with six tea garden soils. The dissipation coefficients of oxyfluorfen in soils of different moisture content (30%, 60%, and
Sunyo Jung et al.
Plant physiology and biochemistry : PPB, 43(5), 423-430 (2005-05-14)
We analyzed the herbicidal and antioxidant defense responses of transgenic rice plants that overexpressed the Myxococcus xanthus protoporphyrinogen oxidase gene. Leaf squares of the wild-type incubated with oxyfluorfen were characterized by necrotic leaf lesions and increases in conductivity and malonyldialdehyde
H M Hassanein et al.
Archives of environmental contamination and toxicology, 37(1), 78-84 (1999-05-26)
This paper deals with the expression of the biomarker hsp70 in the liver and kidney of the freshwater fish Oreochromis niloticus following exposure to the herbicide oxyfluorfen (Goal). Fishes were exposed to three concentrations, the 96-h LC50 (3 mg/L), the
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