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35031

Supelco

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
Beilstein:
2065259
EC Number:
255-983-0
MDL number:
MFCD00072435
UNSPSC Code:
41116107
PubChem Substance ID:
329755114
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

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

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

InChI key

OQMBBFQZGJFLBU-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH2937
BCBW2993
SZBD037XV
SZBB014XV
SZB7017XV

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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)
Laura Scrano et al.
Journal of environmental quality, 33(2), 605-611 (2004-04-13)
The photochemical behavior of oxyfluorfen [2-chloro-1-(3-etoxy-4-nitrophenoxy)-4-(trifluoromethyl) benzene] on two Greek soils was investigated. Soils were sampled from Nea Malgara and Preveza regions, characterized by a different organic matter content. Soils were spiked with the diphenyl-ether herbicide and irradiation experiments were
Iris Sandorf et al.
Planta, 216(1), 173-179 (2002-11-14)
Coronatine-inducible tyrosine aminotransferase (TAT), which catalyses the transamination from tyrosine to p-hydroxyphenylpyruvate, is the first enzyme of a pathway leading via homogentisic acid to plastoquinone and tocopherols, the latter of which are known to be radical scavengers in plants. TAT
Chloé Bonnineau et al.
Ecotoxicology (London, England), 21(4), 1208-1224 (2012-03-13)
In multiple stress situations, the co-occurrence of environmental and chemical factors can influence organisms' ability to cope with toxicity. In this context, the influence of light adaptation on the response of freshwater biofilms to sudden light changes or to herbicides
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